SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs149460 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174520 | tcctgcctcagcctt[C/T]tgagtagctgggatt | 10055 |
rs149527 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174906 | tagagacggggtttc[A/C]ccatgttggccaggc | 10055 |
rs160263 | snp | A/T | 0.131381 | 0.220067 | intron-variant | SAE1 | GRCh38.p7 | 19:47172750 | TCATCTACTCCAGAG[A/T]TGAAAAGTGTACACG | 10055 |
rs160264 | snp | A/C | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47174996 | ttacaggcgtgaggc[A/C]ccgtgcccggcAGTG | 10055 |
rs177918 | snp | G/T | 0.179114 | 0.23974 | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131056 | GCGGCTTGAGGCCGC[G/T]AGGGTCTGGAGGGGG | 10055 |
rs184271 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47160211 | AGAGGTTCAAAATCC[C/T]GCAtttttttttttt | 10055 |
rs186289 | snp | A/C | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47172043 | cccgcctcagcctcc[A/C]gagtagctgggatta | 10055 |
rs186290 | snp | C/T | 0.00569796 | 0.0530708 | intron-variant | SAE1 | GRCh38.p7 | 19:47148954 | TTCATTTCAAGCATT[C/T]TTAATTGTGTCTGAT | 10055 |
rs188658 | snp | A/G | 0.0132444 | 0.080292 | intron-variant | SAE1 | GRCh38.p7 | 19:47183615 | ATGTGGGCCTGCTAA[A/G]AAAAAAAGCAAGGCA | 10055 |
rs188659 | snp | C/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47148578 | GGTGAAATAATTCCT[C/G]TGTTCCAGTCCCCAC | 10055 |
rs192807 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47183040 | taatcccagctactc[G/T]ggaggcagaggcagg | 10055 |
rs307895 | snp | A/C | 0.172351 | 0.237636 | intron-variant | SAE1 | GRCh38.p7 | 19:47184074 | TGACTCTCACCTTTA[A/C]GGTGAAACATTCTAA | 10055 |
rs307896 | snp | C/T | 0.1652 | 0.235179 | intron-variant | SAE1 | GRCh38.p7 | 19:47158236 | CTTTTTGTTTTTCAA[C/T]GTTACTAATTTAGGA | 10055 |
rs307897 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | SAE1 | GRCh38.p7 | 19:47195889 | aaaaaaatttagcca[A/G]gtatggtggtgcctg | 10055 |
rs307898 | snp | C/G | 0.100588 | 0.200439 | intron-variant | SAE1 | GRCh38.p7 | 19:47196617 | cccagcactttggga[C/G]gccgaggcaggtgga | 10055 |
rs307899 | snp | C/T | 0.109814 | 0.206997 | intron-variant | SAE1 | GRCh38.p7 | 19:47197603 | CATTGCCTTGAATTT[C/T]GAACCACGTGAATAT | 10055 |
rs307900 | snp | A/G | 0.44651 | 0.154543 | intron-variant | SAE1 | GRCh38.p7 | 19:47186320 | tgcattgtacttacc[A/G]atagagcaccccaaa | 10055 |
rs307901 | snp | C/T | 0.131038 | 0.219882 | intron-variant | SAE1 | GRCh38.p7 | 19:47186507 | CACAGCAGAGGGGAG[C/T]ACGAATGCTCAATGA | 10055 |
rs307902 | snp | A/G | 0.172351 | 0.237636 | intron-variant | SAE1 | GRCh38.p7 | 19:47189613 | TCCCTGCAGCTGAAC[A/G]TAGACTCCTCCCCAG | 10055 |
rs309182 | snp | C/G | 0.421842 | 0.181577 | intron-variant | SAE1 | GRCh38.p7 | 19:47159459 | CTCCTAGTCCAGTGT[C/G]TAGCACAGTCATATC | 10055 |
rs309183 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SAE1 | GRCh38.p7 | 19:47140906 | tgggatggagtgcag[C/T]ggcacagtcttggct | 10055 |
rs309184 | snp | G/T | 0.449091 | 0.151204 | intron-variant | SAE1 | GRCh38.p7 | 19:47133570 | aataggttaaagtgg[G/T]cagaaatggaagtaa | 10055 |
rs309185 | snp | C/T | 0.390651 | 0.206682 | intron-variant | SAE1 | GRCh38.p7 | 19:47132027 | Tgtgcagttgggtga[C/T]ctcggttcactgcag | 10055 |
rs309186 | snp | C/G | 0.0998734 | 0.199905 | intron-variant | SAE1 | GRCh38.p7 | 19:47131994 | gagtgagccaccgcg[C/G]caggACGTCTTTTGT | 10055 |
rs309187 | snp | G/T | 0.131381 | 0.220067 | intron-variant | SAE1 | GRCh38.p7 | 19:47131759 | aggctggagggcagt[G/T]gcgcgatctcggctc | 10055 |
rs309197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149264 | caacctccgcctccc[C/G]tgttgaagtgattct | 10055 |
rs365128 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177363 | CTGGtttttgtttgt[G/T]ttttttcccccccaa | 10055 |
rs365655 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177416 | caggctggagtgtgg[G/T]ggcacaatcataact | 10055 |
rs368952 | snp | C/T | 0.449726 | 0.150364 | intron-variant | SAE1 | GRCh38.p7 | 19:47179323 | ccagcctgggcaaca[C/T]ggtgaaaccctgtct | 10055 |
rs371300 | snp | G/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191342 | CATTTATTTACTCGT[G/T]TTTGTGTTTCTTCTT | 10055 |
rs371510 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47180340 | attcttagagcactt[C/T]cttactttctggcat | 10055 |
rs374428 | snp | A/T | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191243 | ttgtatttttactag[A/T]gacggggcttcacta | 10055 |
rs377035 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177359 | GTGCCTGGGTTTTGT[G/T]TGTGTTTTTTCCCCC | 10055 |
rs384011 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47177343 | GAAACTATCATGTGT[G/T]GTGCCTGGGTTTTGT | 10055 |
rs384394 | snp | C/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191345 | ATTCATTTATTTACT[C/T]GTGTTTGTGTTTCTT | 10055 |
rs385812 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168626 | GTTGtttttgagaca[C/G]agtttcgctcttgtt | 10055 |
rs392204 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47177352 | ATGTGTGGTGCCTGG[G/T]TTTTGTGTGTGTTTT | 10055 |
rs394537 | snp | G/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130490 | ttatcatagctgggt[G/T]tatatttatttctct | 10055 |
rs413035 | snp | A/C | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47167187 | tccaattcctgacct[A/C]tagtgatccacccgc | 10055 |
rs415138 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47180586 | gatcaatttgcctca[G/T]cctcttgggatttat | 10055 |
rs417369 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183141 | ggctggtctcaaact[A/C]ttgacctcaggtgat | 10055 |
rs425703 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47134688 | AACTTTGCCCCACTT[C/T]AAACAAAGCTATCTG | 10055 |
rs425843 | snp | A/C | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191336 | AAAAAAAAGAAGAAA[A/C]ACAAACACGAGTAAA | 10055 |
rs426064 | snp | A/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47134716 | GTTGGTGAGGTTTAA[A/T]CTGGAATGTAGTTAG | 10055 |
rs431566 | snp | A/T | 0.0998734 | 0.199905 | intron-variant | SAE1 | GRCh38.p7 | 19:47137507 | ACAATTACAACTAAA[A/T]TTTTTTTTtctcgct | 10055 |
rs436885 | snp | A/C | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47180375 | ggggcatgtcaaaag[A/C]acaagaagTATAATC | 10055 |
rs440931 | snp | A/C | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47183113 | tggagatgggctttc[A/C]ccatgttggccaggc | 10055 |
rs441173 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191151 | cgtagtgggtcatgc[A/C]tataatcccagcact | 10055 |
rs443002 | snp | C/T | 0.100944 | 0.200705 | intron-variant | SAE1 | GRCh38.p7 | 19:47135964 | gcccgccaccacgcc[C/T]ggctaatttctgtat | 10055 |
rs443700 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47134896 | CAATCCTTTTCATGT[G/T]CTCCACCAAATTTGG | 10055 |
rs448531 | snp | C/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47180555 | aggggtgagccacca[C/G]gcATAGCATAAAAGC | 10055 |
rs457394 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47168698 | acctcccccctccta[G/T]gttcaagcgattctc | 10055 |
rs458763 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175552 | GGGCAGCCTGGCCAA[A/G]ATGGTGAAATCCCGT | 10055 |
rs461709 | snp | A/G | 0.143622 | 0.226238 | intron-variant | SAE1 | GRCh38.p7 | 19:47163454 | tatgggaggccaggc[A/G]cagtgcctcacgcct | 10055 |
rs463437 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149982 | CAAATGATTCTCCTC[C/G]TGCCTCAGCCTCCCA | 10055 |
rs464328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47168793 | atttttaatagagac[A/G]gggtttcactatgtt | 10055 |
rs464343 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168845 | ctgacctcaggcgat[A/C]cacccgcctctgcct | 10055 |
rs464463 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47168856 | cgatccacccgcctc[G/T]gcctcccaaagtgct | 10055 |
rs464964 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149930 | aaaatacaaaaatta[G/T]ctgttgtggtggtgc | 10055 |
rs465186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47165970 | GGAGAGAGAATCTGA[C/T]TGGCCTGGTTGGGGT | 10055 |
rs465213 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149807 | TTAGggctgtgcaca[C/G]tgtttcatgcctgta | 10055 |
rs465547 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149860 | tcaatctcttgacct[C/T]gtgatccgcctgcct | 10055 |
rs466477 | snp | C/T | 0.387832 | 0.208572 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176541 | ATTGTAGAGGGAGAG[C/T]AGTGTGCCCACTGGA | 10055 |
rs467405 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149808 | ttacaggcatgaaac[A/T]ctgtgcacagccCTA | 10055 |
rs473112 | snp | C/G | 0 | 0 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130735 | GTCACGTGACATGCA[C/G]TCGCCGGATCGCCTT | 10055 |
rs481934 | snp | C/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47134500 | GAGAATGTGCCTCTG[C/G]ACATAGGTGGACTGC | 10055 |
rs482870 | snp | A/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47134588 | GGAGGAAACTTTGAG[A/G]AAGCTTGGTGTGTTC | 10055 |
rs578258 | snp | G/T | 0 | 0 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130183 | aaggcagagatgtgt[G/T]catttttattattat | 10055 |
rs686873 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175443 | TTTCAACATATTTAA[A/G]ATATATCTGTAGTCT | 10055 |
rs694405 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174808 | tcgatgttttgacct[C/T]gtgatccgcctgcct | 10055 |
rs734277 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47158769 | AATTTCTCATAGCTT[C/T]TTTATCAGCTATAGA | 10055 |
rs745826 | snp | A/C | 0.332337 | 0.236052 | intron-variant | SAE1 | GRCh38.p7 | 19:47158598 | TTTATCCTACTTCCT[A/C]GGACAGAGCACTGCT | 10055 |
rs751612 | snp | G/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191343 | tcatttatttacttg[G/T]ttttgtttttcttct | 10055 |
rs751613 | snp | C/T | 0.330947 | 0.236533 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191665 | CAGTTGGTGCTTGTG[C/T]CCCAGTAACAAAGAA | 10055 |
rs1043777 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209587 | GCCAGCCCTCTGGGG[A/C]ATTGTGGGAGATGCC | 10055 |
rs1077336 | snp | C/G | 0.33303 | 0.235809 | intron-variant | SAE1 | GRCh38.p7 | 19:47157877 | CCTTGCCTTTGTGCA[C/G]CCTCACCAAGGGCCC | 10055 |
rs1644747 | snp | A/G | 0 | 0 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129873 | ccaggttggagtgca[A/G]aggcatgatcttggc | 10055 |
rs1644748 | snp | A/C | 0.131381 | 0.220067 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129953 | TTCCAAGTAGCTGGG[A/C]CTACAAGTGTGAGCC | 10055 |
rs1644749 | snp | C/G | 0 | 0 | upstream-variant-2KB, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47130804 | ACGAGGTACTGCGCA[C/G]GCGTGGGAGGGTCTG | 10055 |
rs1644750 | snp | C/G | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130830 | GTCTGCGCATGCGCA[C/G]AAGCACTCCGGGCGT | 10055 |
rs1644751 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130833 | TGCGCATGCGCAGAA[A/G]CACTCCGGGCGTGCT | 10055 |
rs1686785 | snp | G/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130108 | aggtgcgagtcaccg[G/T]gcctggccTATTCCT | 10055 |
rs2161241 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47189184 | AAATTTCCAGAAAAA[C/T]TGCAAAGTATGGTAG | 10055 |
rs2431396 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176976 | TGAATGCTGTTTCCA[C/T]ACCAGACTCGGTATT | 10055 |
rs2547408 | snp | A/G | 0.464416 | 0.128553 | | | GRCh38.p7 | 19:47144642 | gcatgatctcggctc[A/G]ttgcaagctccgcct | 10055 |
rs2635773 | snp | A/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47145901 | CCGTGAGCATCTTTC[A/T]atcaccagcacctag | 10055 |
rs2909902 | snp | A/T | 0.143959 | 0.226396 | intron-variant | SAE1 | GRCh38.p7 | 19:47164069 | CCATTGCACCTGGCT[A/T]GTATATGTGTATATA | 10055 |
rs3745621 | snp | C/G | 0.384785 | 0.210554 | intron-variant | SAE1 | GRCh38.p7 | 19:47186664 | AGGTTCCGAGGCGCC[C/G]GATGAAAGTTGTTGA | 10055 |
rs3760765 | snp | A/G | 0.331642 | 0.236293 | intron-variant | SAE1 | GRCh38.p7 | 19:47189904 | TTAGCGCTATAACGG[A/G]AATCTGGACAGCAAC | 10055 |
rs4802332 | snp | C/G | 0.225597 | 0.248806 | intron-variant | SAE1 | GRCh38.p7 | 19:47138660 | TCTGGAGTTTACATT[C/G]TAATGGAGGAGGGGG | 10055 |
rs4802335 | snp | A/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47157198 | TAAGTGTGATACAGA[A/G]GAATTAAGCCCTAAT | 10055 |
rs4804028 | snp | C/G | 0.334871 | 0.235153 | intron-variant | SAE1 | GRCh38.p7 | 19:47147822 | ggagtgcagtggcgc[C/G]atcttggctcactgc | 10055 |
rs6509312 | snp | A/G | 0.371177 | 0.218669 | intron-variant | SAE1 | GRCh38.p7 | 19:47179274 | actttgggaggctga[A/G]gcaggtggattgcct | 10055 |
rs6509314 | snp | C/T | 0.200182 | 0.244986 | intron-variant | SAE1 | GRCh38.p7 | 19:47193369 | cctggccAATTGTTA[C/T]AGCTTTGAGTTGACT | 10055 |
rs7246226 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47138852 | AGACCCCATCTTAAT[A/C]AAAACAAAAACAAGT | 10055 |
rs7250009 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SAE1 | GRCh38.p7 | 19:47198364 | tgatccgcctacctt[A/G]gcctcccaaagtgct | 10055 |
rs7251708 | snp | A/G | 0.389715 | 0.207315 | intron-variant | SAE1 | GRCh38.p7 | 19:47186440 | TAATTCATTCAGCGG[A/G]TAAGGGTCAGGACCT | 10055 |
rs7252221 | snp | C/T | 0.371177 | 0.218669 | intron-variant | SAE1 | GRCh38.p7 | 19:47179075 | cgggcgtctgtagtc[C/T]cagctacttgggagg | 10055 |
rs7254926 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179607 | ctggagtgcagtgtc[A/G]cgatcataacttact | 10055 |
rs7255338 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47200767 | tttatatattatctg[G/T]ggcagcttttgtgcc | 10055 |
rs7256607 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SAE1 | GRCh38.p7 | 19:47166221 | GGTAGCTACACTCAA[A/G]TGCAGAGCCACCAGT | 10055 |
rs7409320 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SAE1 | GRCh38.p7 | 19:47193219 | cccaccaccatgcac[A/G]gctaatttttttggt | 10055 |
rs8100413 | snp | A/G | 0.0704125 | 0.17392 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130395 | aaAATTGAcagttca[A/G]tgtcacctctgataa | 10055 |
rs8101491 | snp | A/G | 0.45866 | 0.137698 | intron-variant | SAE1 | GRCh38.p7 | 19:47139523 | aacgatggtggctca[A/G]actagagtggtgttt | 10055 |
rs8102394 | snp | G/T | 0.331642 | 0.236293 | intron-variant | SAE1 | GRCh38.p7 | 19:47172833 | AGTTCTCTAGGACTT[G/T]CTCTGTGCCGGGCGT | 10055 |
rs8102445 | snp | G/T | 0.440471 | 0.161928 | intron-variant | SAE1 | GRCh38.p7 | 19:47134351 | TTAGAGGGTGCAGTG[G/T]TGGGATGGGAATTAC | 10055 |
rs8107443 | snp | G/T | 0.39979 | 0.200158 | intron-variant | SAE1 | GRCh38.p7 | 19:47204170 | CTCTATTCATCACCA[G/T]GACATCAAAGCCCTC | 10055 |
rs9630861 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SAE1 | GRCh38.p7 | 19:47173835 | tgtcacccaggctgg[A/G]gtgcagtggtgcaat | 10055 |
rs10409846 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47147061 | GAAAGATAAGTAATT[C/T]TGAGATGGAAGCTTG | 10055 |
rs10415835 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47174390 | aatAATCATACAATG[G/T]tttattttattttgt | 10055 |
rs10419833 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | SAE1 | GRCh38.p7 | 19:47136034 | gtctcaatctcctga[C/G]ctcgtgtaccacaat | 10055 |
rs10423223 | snp | A/G | 0.420096 | 0.183214 | intron-variant | SAE1 | GRCh38.p7 | 19:47193079 | TTTTTTTTTTTGGAG[A/G]CAGAGTCTTGCTCTG | 10055 |
rs10424953 | snp | A/G | 0.429987 | 0.173507 | intron-variant | SAE1 | GRCh38.p7 | 19:47202026 | GAATGTGCTGGTCCT[A/G]GCCAGGGCGTAAGGA | 10055 |
rs10425145 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SAE1 | GRCh38.p7 | 19:47133019 | tgagcctcagactta[C/T]atgggaaagagccct | 10055 |
rs10582931 | in-del | -/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47137730 | GTGTGTGTGTGTTGT[-/G]TTTTTTTTTTTTTTT | 10055 |
rs10606115 | in-del | -/TG | 0.5 | 0 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190346 | CAGTCAACAGTGGTA[-/TG]TGTGCGTGTTTGGCT | 10055 |
rs11083862 | snp | A/T | 0.459233 | 0.136827 | intron-variant | SAE1 | GRCh38.p7 | 19:47135282 | TATTCATTGTATTTA[A/T]TTATATTTTTGTATC | 10055 |
rs11083864 | snp | C/T | 0.0363453 | 0.129814 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197354 | GGGTATTAGTCCTGA[C/T]CTGCTTCCTGAGGAC | 10055 |
rs11291244 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47205321 | TTTTCCTAAGGCTAC[-/T]TTTTTTTTTTTTTTT | 10055 |
rs11321351 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47145955 | TTTTTTTTTTTTTTT[-/T]CCGGAAACCATAGCA | 10055 |
rs11366843 | in-del | -/A | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47188350 | CTGAGGCCATGTCTC[-/A]AAAAAAAAAAAGAAA | 10055 |
rs11418627 | in-del | -/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146049 | AAAGAACAAGGAGGG[-/T]TTGTCAAGATAAGAG | 10055 |
rs11456095 | in-del | -/T/TT | 0.453939 | 0.144598 | intron-variant | SAE1 | GRCh38.p7 | 19:47161182 | TTTTTTTTTTTTTTT[-/T/TT]GAGATCTCTTGCTGT | 10055 |
rs11559276 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155164 | TAGAAGATGGGCCCG[A/G]CACCAAGAGAGCAAA | 10055 |
rs11559278 | snp | A/C | 0 | 0 | missense, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143555 | GCTGAAATTGCCAAG[A/C]ATCTCATCTTGGCAG | 10055 |
rs11559279 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209749 | TGGAAGCACAGCTCC[A/C]AGTTCAGACAGGTGC | 10055 |
rs11666272 | snp | C/T | 0.310888 | 0.242472 | intron-variant | SAE1 | GRCh38.p7 | 19:47155063 | TTTTTTTGATTCCAA[C/T]AACATGATTCCTAGG | 10055 |
rs11667301 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47134809 | TGAGTGGGAGATGAC[C/T]TAAGGGACAAGTCAG | 10055 |
rs11667537 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149161 | caggctGCACTGGTC[C/T]ACttttttttttttt | 10055 |
rs11667609 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47179468 | gccgaggttgctcca[C/T]tgcactccagcctgg | 10055 |
rs11668747 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174588 | ttttttttttttttt[G/T]gtgagacggagtctc | 10055 |
rs11669489 | snp | A/T | 0.332799 | 0.23589 | intron-variant | SAE1 | GRCh38.p7 | 19:47196848 | AGGTAAATTGCTTTT[A/T]TAATTATTGGATTGC | 10055 |
rs11670191 | snp | A/G | 0.310599 | 0.242552 | intron-variant | SAE1 | GRCh38.p7 | 19:47155225 | AAAGGTATGTGTAAC[A/G]TGGGGGCAGAGGTCA | 10055 |
rs11670947 | snp | C/G | | | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131051 | CCGGCGCGGCTTGAG[C/G]CCGCTAGGGTCTGGA | 10055 |
rs11671203 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139776 | ttttttttttttttg[G/T]atttttagtagaaac | 10055 |
rs11671631 | snp | A/G | 0.343924 | 0.231686 | intron-variant | SAE1 | GRCh38.p7 | 19:47144155 | cctggccaacatggc[A/G]aaactctgtctgtac | 10055 |
rs11879951 | snp | A/G | 0.375 | 0.216506 | intron-variant | SAE1 | GRCh38.p7 | 19:47165788 | AAAGGATTGTTAAGT[A/G]GAGTGTAAGAAGCAC | 10055 |
rs12232824 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47154297 | ggtttcactatgttg[G/T]ctatgctggtcttga | 10055 |
rs12611339 | snp | A/G | 0.124837 | 0.216412 | intron-variant | SAE1 | GRCh38.p7 | 19:47180827 | gtctcCCCCGAAAAA[A/G]AAGATGCTTTTAAAT | 10055 |
rs12611429 | snp | A/G | 0.332337 | 0.236052 | intron-variant | SAE1 | GRCh38.p7 | 19:47145572 | CCATGCCTCAGTGAC[A/G]ttttatttattttat | 10055 |
rs12973505 | snp | C/T | 0.403158 | 0.197592 | intron-variant | SAE1 | GRCh38.p7 | 19:47200561 | tttttgttgtagaga[C/T]gggggtctcactctg | 10055 |
rs12975381 | snp | A/G | 0.353299 | 0.227661 | intron-variant | SAE1 | GRCh38.p7 | 19:47171294 | GCACTTTTAAttttt[A/G]ttttaattttttttt | 10055 |
rs12979152 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167956 | ccaacactttgggag[A/C]ccgaggcaggcagat | 10055 |
rs12979581 | snp | C/T | 0.36021 | 0.224397 | intron-variant | SAE1 | GRCh38.p7 | 19:47182461 | GGAAAAAGAAAAAAG[C/T]GTAGTGTGTGTGTGT | 10055 |
rs13313713 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47140083 | gctgagattacaggc[A/G]cctgccaccactccc | 10055 |
rs13343481 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193604 | aggtgggaggatcac[A/C]tgaggtcaggaactt | 10055 |
rs16980850 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47170125 | GTTCTAATGACTTCT[C/G]CTTTTTTTACTTGTT | 10055 |
rs16980852 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SAE1 | GRCh38.p7 | 19:47172808 | AAGCACATATCTTCA[C/T]GGATGACAGAGTTCT | 10055 |
rs17369550 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47208200 | ATTATTTCTGCTGTT[G/T]GCCCAATGGTGGTGC | 10055 |
rs17729227 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SAE1 | GRCh38.p7 | 19:47161694 | TTGAAGCATCAAACA[C/T]TACTGGTATGGTGAG | 10055 |
rs17729245 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SAE1 | GRCh38.p7 | 19:47172809 | AGCACATATCTTCAC[A/G]GATGACAGAGTTCTC | 10055 |
rs17802270 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SAE1 | GRCh38.p7 | 19:47167650 | CAAATTATGCTGTTA[C/T]CATCTTGTCTCTCTG | 10055 |
rs28375607 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47182514 | GCGCACGCACGCGCG[C/T]GCGCACACCACTGCC | 10055 |
rs28399748 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207009 | TGCTTAATAAATGTT[A/C]CCTTGACTGGGTGCA | 10055 |
rs28403930 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194853 | GTTCAAGTGATTCTT[C/G]TGCTTCAGCCTCCCA | 10055 |
rs28447566 | snp | G/T | 0.0115649 | 0.0751579 | intron-variant | SAE1 | GRCh38.p7 | 19:47155469 | CCCAAACTTTTTTTT[G/T]TGTGTGTGTGAGATG | 10055 |
rs28608780 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47192407 | GCGTCCGCCACCATG[C/T]CCAGCTAATTTTTGT | 10055 |
rs28733076 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174299 | TTCTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 10055 |
rs34071641 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47153884 | CAATCTCTGCCTCCT[-/G]GGGTTCAAGCCATTC | 10055 |
rs34105470 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47178410 | AAATCAGCCAAGTTA[-/G]GGGGAAAGTACTGTC | 10055 |
rs34159938 | snp | A/G | 0.389903 | 0.207189 | intron-variant | SAE1 | GRCh38.p7 | 19:47187554 | CTGAGCCAGGGTCTC[A/G]CTTTGTCACCCAGCT | 10055 |
rs34180997 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162574 | TAAAGCTTTTTAAAG[-/A]ATTCTTGGTCCCTCT | 10055 |
rs34218710 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47157276 | TTTTGGCCAAAACTT[-/G]GGGTGCCTTTCTTTC | 10055 |
rs34266912 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47160412 | TTTTTTTTTTTTTTT[-/T]GAGATGGACTCTCGC | 10055 |
rs34283144 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195611 | CTTTAAACTGGTCCT[-/G]GCCTAGAATGTGTAC | 10055 |
rs34286215 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47176116 | TATGTAATCAAACTG[-/T]TGAAACACCGGTTGG | 10055 |
rs34344630 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47134769 | TGATTTTTCTGAGAA[A/G]CAGTGAAGAATGGAT | 10055 |
rs34349715 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175395 | GACAGTCAGAATTTA[A/G]ACCATGAGGTTTGTT | 10055 |
rs34368525 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201314 | GCCTCCGAAAGTGCT[-/G]GGGATTACAGGCATG | 10055 |
rs34368873 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139615 | TTTTTGAGACAGAGT[-/A]CTCACTCTTGTCACC | 10055 |
rs34395453 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210457 | TAATAAAGGGAAGTC[-/A]AAAAGTGATGCTTCA | 10055 |
rs34440742 | in-del | -/A | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47150074 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 10055 |
rs34507064 | snp | C/T | 0.332799 | 0.23589 | intron-variant | SAE1 | GRCh38.p7 | 19:47161749 | AAGTTACCACCCTCC[C/T]CAGTTGGGTTTCTCA | 10055 |
rs34530794 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163030 | AATAAGTTCATAATT[-/C]CCAAATGTGGAAAAT | 10055 |
rs34538392 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175380 | TCCGTGGTTTTATAG[-/C]ACAGTCAGAATTTAG | 10055 |
rs34563423 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47161742 | CAACAGAAGTTACCA[-/C]CCCTCCTCAGTTGGG | 10055 |
rs34575308 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47139955 | CCACTTGGGTATTTC[-/T]TTTTTTTTTTTTTTT | 10055 |
rs34624684 | snp | G/T | 0.00865784 | 0.0652224 | intron-variant | SAE1 | GRCh38.p7 | 19:47161446 | CAATCTGTATGCTGT[G/T]TCTCTATCTTCTACT | 10055 |
rs34758939 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137748 | TTTTTTTTTTTTTTG[G/T]GATGGACTCTCACTC | 10055 |
rs34800424 | snp | A/T | 0.245061 | 0.249951 | intron-variant | SAE1 | GRCh38.p7 | 19:47191974 | CAGGAGAATGGCGTG[A/T]ACCCGGGAGGCGGAG | 10055 |
rs34802818 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47175467 | GTAGTCTGGGCGCGG[G/T]GGCTTATGCCTGTAA | 10055 |
rs34836827 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170503 | TCACCGCCCCCCGCC[-/T]TTTTTTTTTTTTTTT | 10055 |
rs34964355 | in-del | -/A | 0.459687 | 0.136129 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130367 | GACCCCATCTCTATG[-/A]AAAAAAAAAAAAAAA | 10055 |
rs35006784 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204501 | CTGTACCCAGCCGCA[-/C]CCCCCCCCCTTTTTT | 10055 |
rs35241626 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141932 | CCTTTTTGAAATCTG[-/A]AAAAATTGTGACTCT | 10055 |
rs35275499 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199391 | GGGAGACTCCTTCTC[-/A]AAAAAAAAAAAAAAA | 10055 |
rs35275776 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170487 | GATCAACCAACTTCT[C/T]TTCACCGCCCCCCGC | 10055 |
rs35290065 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200512 | TATACAAAGCACATC[-/G]TGCCTGAGTTAAATG | 10055 |
rs35368210 | snp | A/G | 0.489318 | 0.0722982 | intron-variant | SAE1 | GRCh38.p7 | 19:47196450 | TTCACTGCAACTTCC[A/G]CCTGCTGGATTCAAG | 10055 |
rs35374865 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47135797 | TTTGTACCACAATTT[-/A]CTATTTTTTTTTTTG | 10055 |
rs35404075 | snp | A/G | 0.375 | 0.216506 | intron-variant | SAE1 | GRCh38.p7 | 19:47184062 | TTTTCATACTAGTTA[A/G]AATGTTTCACCTTAA | 10055 |
rs35426762 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47145713 | GCTTCCCTAGTAGCT[-/G]GGGATTACATAATTA | 10055 |
rs35463823 | in-del | -/T | 0.402454 | 0.198136 | intron-variant | SAE1 | GRCh38.p7 | 19:47136512 | ATTTTTACCCGAGTC[-/T]TTTTTTTTTTTTTTT | 10055 |
rs35545384 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47162571 | TTGTTAAAGCTTTTT[-/A]AAGATTCTTGGTCCC | 10055 |
rs35592429 | in-del | -/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47178211 | TCGCGCCACTGCACT[-/C]CAGCCTGACGACAGG | 10055 |
rs35657499 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200400 | ACCAAGCCTGCCTAA[-/T]TTTTTTTTTTTTTTT | 10055 |
rs35709169 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47199975 | TCGCTCTGTCCCCCA[-/G]GCTGGAGTGCGATGG | 10055 |
rs35966526 | snp | A/G | 0.00253368 | 0.0355024 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169841 | CTTCTGCCCTGTTAA[A/G]GAAGCCCTGGAGGTG | 10055 |
rs35967352 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184003 | TTGTCCACATTATTT[-/C]CCCTGTGACTTTTAG | 10055 |
rs35991953 | in-del | -/GT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137715 | AACACTCAGCTGATT[-/GT]GTGTGTGTGTGTGTG | 10055 |
rs55801246 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47147232 | TTTTTTTTTTTGAGG[C/T]AGTCTCACTGTTACC | 10055 |
rs55861101 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137209 | GCCTGGCCAACATGG[A/T]GACCGTCTCTACTAA | 10055 |
rs55969087 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156490 | CTCCAAAAAAAAAAG[C/T]TTTCTTTGCCTGTTT | 10055 |
rs56173755 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156056 | AAAACTTTTTTTTTT[A/T]AAGCAGCAAAACACC | 10055 |
rs56179616 | snp | G/T | 0.389152 | 0.207694 | intron-variant | SAE1 | GRCh38.p7 | 19:47192494 | CCTCGTGATCCACCC[G/T]CCTTGGCCTCCCAAA | 10055 |
rs56206314 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155936 | AGTAGAGACGGGGTT[C/T]CACCATGTTGGCCAG | 10055 |
rs56217044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47195791 | CCCAGGCTGGAGTGC[A/G]GTGATGAGATCTCTG | 10055 |
rs56268362 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47195737 | TTCCTTTTTTTCTTC[-/T]TTTTTTTTTTTTTTT | 10055 |
rs56312736 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SAE1 | GRCh38.p7 | 19:47200957 | CCACCTCCCGGGTTC[A/G]AGTGAATCTCCTGCC | 10055 |
rs56357219 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156545 | AATAAGAAAAATCCT[C/T]CAATGTT | 10055 |
rs56371077 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200591 | GCTGCCCAGGCTGTT[C/T]TCAGACTCCTGGATT | 10055 |
rs56405554 | snp | A/G | | | missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209215 | CTTCGATGGCATGAA[A/G]GGGAATGGGATTGTG | 10055 |
rs56699739 | in-del | -/CTTT | 0.499187 | 0.0201513 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129804 | TTTCTTTCTTTCTTT[-/CTTT]TTTTTTTTTTTTTAC | 10055 |
rs56892137 | in-del | -/TC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137211 | TGGCCAACATGGTGA[-/TC]CCGTCTCTACTAAAA | 10055 |
rs57186863 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137163 | AGAGGCCGAGGTGGG[C/T]GGATCACCTGAGGTC | 10055 |
rs57293528 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | SAE1 | GRCh38.p7 | 19:47200985 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGATTACGG | 10055 |
rs57564170 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130166 | GGGCCGTGACTGCCT[C/T]TAAGGCAGAGATGTG | 10055 |
rs57568797 | in-del | -/TTTTTTTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47201381 | TTTTTTTTTTTTTTT[-/TTTTTTTTT]GAATCAGAGTCTTGC | 10055 |
rs57634179 | snp | A/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47156318 | TATTTTCTCTACTAA[A/C]AATACAAAAATTAGC | 10055 |
rs57736880 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204215 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 10055 |
rs57805163 | in-del | -/AAGAAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193860 | GAAAAGAAAAAGAAA[-/AAGAAA]TTACCTCTTCTCTGA | 10055 |
rs57870733 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47154510 | TTTTTTTTTTTTTTT[-/T]CTGAGACAGACTTTC | 10055 |
rs57883574 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | SAE1 | GRCh38.p7 | 19:47173359 | CATATAGCTACTGTT[A/T]CTTCCTCAACCACCT | 10055 |
rs58070154 | in-del | -/GA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137210 | CTGGCCAACATGGTG[-/GA]ACCGTCTCTACTAAA | 10055 |
rs58733915 | in-del | -/GA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163300 | AATAAAATATTTGGG[-/GA]AAAAAACATTGCGTC | 10055 |
rs58753357 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137199 | TTCGAGACTAGCCTG[A/G]CCAACATGGTGACCG | 10055 |
rs59138511 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47195075 | TTTTTTTTTTTCTGA[A/G]ATGAAGTCTCACTCT | 10055 |
rs59160052 | snp | C/G/T | 0.0142839 | 0.0833853 | intron-variant | SAE1 | GRCh38.p7 | 19:47143424 | AAAATGATTTGTGTA[C/G/T]TTTTTGTTCTTCTGT | 10055 |
rs59178466 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149494 | TCTAGTTTTAAACCA[C/T]TGGAAGACAGAGATT | 10055 |
rs59197533 | snp | C/T | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129168 | AGGCATGGTGGCTCA[C/T]ACCTGTAATCCGTGC | 10055 |
rs59205144 | in-del | -/GT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137727 | TGTGTGTGTGTGTGT[-/GT]TGTTTTTTTTTTTTT | 10055 |
rs59337755 | snp | A/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129169 | GGCATGGTGGCTCAC[A/G]CCTGTAATCCGTGCA | 10055 |
rs60208381 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184007 | TCCACATTATTTCCC[-/T]GTGACTTTTAGATTT | 10055 |
rs60424665 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47137155 | GGACTTTGAGAGGCC[A/G]AGGTGGGTGGATCAC | 10055 |
rs60528203 | in-del | -/AAAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137235 | ACTAAAAATACAAAA[-/AAAA]TTAGCCAGGTGTGGT | 10055 |
rs60901263 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132905 | AAAAAAAAAAAAAAA[-/A]TCCACAAGCGTGTGT | 10055 |
rs61074057 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47170524 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 10055 |
rs61498882 | in-del | -/TTTT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196364 | TTTTTTTTTTTTTTT[-/TTTT]AATTTTACTTTTTTG | 10055 |
rs62135075 | snp | A/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129094 | AAATGCTGGGATTAC[A/G]GGCGTGAGCCACCAC | 10055 |
rs62135076 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129258 | ACATGGTGCAATCCC[C/T]GTCTCTACTAAAAAT | 10055 |
rs62135077 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | SAE1 | GRCh38.p7 | 19:47138756 | GGGAGGCTGAGGTTG[G/T]AGGATCACTTGAGCC | 10055 |
rs62135078 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47150099 | AAAAAAAAAAAATTT[A/T]GGTGGTAGGTATTTT | 10055 |
rs62135079 | snp | G/T | 0.209693 | 0.246729 | intron-variant | SAE1 | GRCh38.p7 | 19:47155500 | GAATTTTTTCTTGTC[G/T]CTCAGGCTGGAGTGC | 10055 |
rs62135080 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47163250 | GTGCTTGGAGTACAT[A/C]CAAAAAAAAAAAAAG | 10055 |
rs62135081 | snp | A/G | 0.210301 | 0.246828 | intron-variant | SAE1 | GRCh38.p7 | 19:47166380 | GGTGGTTATGAAGAA[A/G]GCGAGTTTGTCAAGA | 10055 |
rs62135082 | snp | A/C | 0.000329522 | 0.0128317 | intron-variant | SAE1 | GRCh38.p7 | 19:47169797 | ATGTTATTCCTAAGC[A/C]GTTCTGCCTTTTTTC | 10055 |
rs62135083 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | SAE1 | GRCh38.p7 | 19:47178114 | GGCATGGTGGTGTGC[A/G]CCTGTAGTCCCAGCT | 10055 |
rs62135084 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47193076 | TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTTGCT | 10055 |
rs62135086 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47199210 | GCTAACATGGTGAAA[A/C]CCCATCTCTACTAAA | 10055 |
rs62135087 | snp | A/G | 0.215144 | 0.247558 | intron-variant | SAE1 | GRCh38.p7 | 19:47208545 | TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 10055 |
rs62135088 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47209092 | CTAGACTGCTTTTAG[A/T]ATTTTTTTTTCCCTC | 10055 |
rs67755129 | in-del | -/TT | 0.375 | 0.216506 | intron-variant | SAE1 | GRCh38.p7 | 19:47200422 | TTTTTTTTTTTTTTT[-/TT]GTATTGACAGGGTCT | 10055 |
rs67933882 | in-del | -/T | 0.372794 | 0.217765 | intron-variant | SAE1 | GRCh38.p7 | 19:47145937 | TTCCCATTCTCAAGG[-/T]TTTTTTTTTTTTTTT | 10055 |
rs68074405 | in-del | -/TG | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137704 | TAACACTCAGCTGAT[-/TG]TGTGTGTGTGTGTGT | 10055 |
rs70954413 | multinucleotide-polymorphism | GT/TG | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47137729 | TGTGTGTGTGTGTGT[GT/TG]TTTTTTTTTTTTTTT | 10055 |
rs71179298 | in-del | -/T | 0 | 0 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129316 | TTTTTTTTTTTTTTT[-/T]AGACGGGAGTCTCTG | 10055 |
rs71179299 | in-del | -/TT | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47139605 | TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCAC | 10055 |
rs71180803 | in-del | -/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47174588 | TTTTTTTTTTTTTTT[-/T]GTGAGACGGAGTCTC | 10055 |
rs71180804 | in-del | -/A | 0.375 | 0.216506 | intron-variant | SAE1 | GRCh38.p7 | 19:47186252 | AAAATAAAAAAAAAA[-/A]TAATAAAAGCTCATT | 10055 |
rs71180805 | in-del | -/TTTTTT | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47196362 | TTTTTTTTTTTTTTT[-/TTTTTT]AATTTTACTTTTTTG | 10055 |
rs71332975 | in-del | -/T/TTTT | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47154480 | AGAATTAAGTTTGGC[-/T/TTTT]TTTTTTTTTTTTTTT | 10055 |
rs71332976 | in-del | -/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47174563 | ACCACGCCTGGCAAA[-/T]TTTTTTTTTTTTTTT | 10055 |
rs71353950 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47136229 | GTACAATCTCCACCT[C/T]CCAGGTTCAAGCGAT | 10055 |
rs71353951 | snp | A/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47138427 | ATTGTCATGGGAATT[A/T]AATGACATAATACAT | 10055 |
rs71353952 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47144655 | AACGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 10055 |
rs71353953 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47155250 | AGGTCAGAAACCCTG[A/G]GGCCTTGGAGGGGTC | 10055 |
rs71363725 | snp | C/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47179408 | GCTACTTGGGAGGCT[C/G]AGGCAGGAGAATTGC | 10055 |
rs71363726 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47188375 | AAGAAAAAAATAATC[A/C]CAAACTGTGAGTAAG | 10055 |
rs71363727 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47193841 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAAG | 10055 |
rs71363728 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47196066 | TTTTTTTTTTTCCCA[A/G]ACGGAGTCTCGCTCT | 10055 |
rs71363729 | snp | A/G | 0.3746 | 0.216737 | intron-variant | SAE1 | GRCh38.p7 | 19:47200919 | CTAGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT | 10055 |
rs73061320 | snp | C/T | 0.443464 | 0.15834 | intron-variant | SAE1 | GRCh38.p7 | 19:47182496 | GTGTGTGTGTGTGTG[C/T]GCGCGCACGCACGCG | 10055 |
rs73061321 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47184777 | TGACATGGTTGTGGG[G/T]TTTTTTTTGTTTTTG | 10055 |
rs73568418 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | SAE1 | GRCh38.p7 | 19:47157708 | TGCAGCCTCTTCCTA[C/G]GTGGAGCTGAGCTGG | 10055 |
rs73568426 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47166177 | GCTTAGGCCAGAGAC[G/T]TGGGGGTTTGGTGAG | 10055 |
rs73568483 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SAE1 | GRCh38.p7 | 19:47170593 | TTCACTGTAGCCTCT[A/G]CTTCCTGGGCTTAAG | 10055 |
rs73568491 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176878 | CAAAACAGTAAGCGT[A/G]AGCTGGTTTCCTGTG | 10055 |
rs73568501 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188580 | GTTTCTGGACTTTGC[G/T]TAAGAGCAGTGACAG | 10055 |
rs73570503 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | SAE1 | GRCh38.p7 | 19:47189147 | TTGCCTTAGGAAACA[A/G]GCTGTTGGATAAGAG | 10055 |
rs73943643 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | SAE1 | GRCh38.p7 | 19:47198686 | CCAGAGTCCCTAGTC[C/T]TTTCTTTGTTGACTT | 10055 |
rs74254136 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | SAE1 | GRCh38.p7 | 19:47180829 | CTCCCCCGAAAAAGA[A/C]GATGCTTTTAAATGA | 10055 |
rs74366019 | snp | C/T | | | intron-variant, missense | SAE1 | GRCh38.p7 | 19:47205117 | AGGTTCTTGGCTGCC[C/T]TCGTGGACTCCGGTG | 10055 |
rs74368789 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47167287 | GTATTTTTTTTTTTT[G/T]TGAGAGTCTCGCTCT | 10055 |
rs74405758 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47193074 | TTTTTTTTTTTTTTT[G/T]GGAGACAGAGTCTTG | 10055 |
rs74490361 | snp | A/T | 0.029116 | 0.117091 | intron-variant | SAE1 | GRCh38.p7 | 19:47168223 | AAAACAAAAAACTGT[A/T]TTTTTGTATGTGTGT | 10055 |
rs74524896 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47177851 | AGAGGGAAGAATATT[A/G]CAGAGCAACACATGC | 10055 |
rs74542105 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47142975 | CGCCTTATTTCCACA[A/C]CATAGAAGGATGCCT | 10055 |
rs74567158 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47172429 | GCTTGTTGCTCACTG[C/T]CTCGCACATAGAAAG | 10055 |
rs74595849 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SAE1 | GRCh38.p7 | 19:47166853 | CATTGACCAAAAGAT[G/T]TGAGGGCAGTGAAAA | 10055 |
rs74622132 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47167289 | ATTTTTTTTTTTTTT[G/T]AGAGTCTCGCTCTGT | 10055 |
rs74629355 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184617 | GGTTTCACCACGTTG[A/G]CCAGGCTACTCTTGA | 10055 |
rs74721503 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47132266 | CTGTGCCCAGCTTGT[G/T]TTTTTTTTTTTTCTT | 10055 |
rs74749546 | in-del | -/TT | | | intron-variant | SAE1 | GRCh38.p7 | 19:47132438 | TGTTTTTTTTTTTTT[-/TT]GTAGGATGGGGTTTT | 10055 |
rs74756802 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SAE1 | GRCh38.p7 | 19:47203429 | CTTATAAAGGTAAAA[A/C]TAAAAGTATTGTGAA | 10055 |
rs74831440 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47178976 | AGGTGGGTGGCTCAC[A/C]GGGTCAGGAGATCGA | 10055 |
rs74893524 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47150945 | CAGCCTCATTTAGTT[G/T]CACTGCCAAATCTAT | 10055 |
rs74970930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158404 | TGCTCAGGAGAAGAT[C/T]TGAGACGGATTTCGT | 10055 |
rs74993468 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47153280 | GAGATAGTAAAATGA[G/T]TACAAAATAGTTGGG | 10055 |
rs75159783 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | SAE1 | GRCh38.p7 | 19:47136785 | ATGAGCCACAGCCCC[C/T]GGCCTTCACCTGAGT | 10055 |
rs75187105 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47166970 | AACTTTTTTTTTTTT[G/T]AGACGGCGTCTCACC | 10055 |
rs75284488 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SAE1 | GRCh38.p7 | 19:47162680 | TATATTACTTGTTAC[C/T]GTTAGGCCTGATTTA | 10055 |
rs75338616 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47175806 | CTGGAGTTCTGTGAG[A/T]TAGGGAAACAGGATC | 10055 |
rs75377923 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47194683 | AATGCCTGCCCGCCC[A/G]CAGGCAGGTTACCTG | 10055 |
rs75385988 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47135025 | CAGCCGAGGTTTTTA[G/T]AAATTAAAAATTTTT | 10055 |
rs75438635 | snp | C/T | 0.151334 | 0.229706 | intron-variant | SAE1 | GRCh38.p7 | 19:47182498 | GTGTGTGTGTGTGTG[C/T]GCGCACGCACGCGCG | 10055 |
rs75441740 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47207753 | GATCCTCCCACCTCA[C/G]CTTCCTGAGGCACTG | 10055 |
rs75521901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47172917 | CACCACCAGCTACAG[A/G]GGGGAATCTGAGGCT | 10055 |
rs75562970 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SAE1 | GRCh38.p7 | 19:47185240 | TCAATATGTCTTTAT[A/G]TGTGGTACAGACTGA | 10055 |
rs75573168 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47162100 | CATAGCACAGATTAC[A/G]TTCTGTTCCATCATC | 10055 |
rs75602607 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47211026 | AGGGGAAAGCTGCCA[G/T]CCCCAGGCAAGAAAT | 10055 |
rs75615825 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47154867 | ATTTATTGAGAGCAG[C/T]TGTGTGCCCAGCAGT | 10055 |
rs75776615 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47183865 | GAGACAAGACCCTCT[C/T]TCCCTGCTGCTTGTG | 10055 |
rs75781174 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47206680 | CATCTCCTGTATCTT[G/T]GGTTTGAGGGTCTAA | 10055 |
rs75790361 | snp | A/G | 0.133093 | 0.220981 | intron-variant | SAE1 | GRCh38.p7 | 19:47207190 | AGGTTGCAGTAAGCC[A/G]AGAATGTGCCTCCCA | 10055 |
rs75803625 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47200236 | CCACGCCCAGCCTCT[C/T]TTTTTTTTTTTTTTT | 10055 |
rs75892488 | snp | C/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47196439 | CACAATCTTGGTTCA[C/G]TGCAACTTCCGCCTG | 10055 |
rs75924607 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47154482 | GAATTAAGTTTGGCT[C/T]TTTTTTTTTTTTTTT | 10055 |
rs76161073 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47158615 | GGAAGTAGGATAAAC[C/G/T]GAAAGACGGACGTAG | 10055 |
rs76172576 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47168319 | CAGTCTGTATTTTTT[C/T]CTCTCTCTCTCTGTT | 10055 |
rs76278517 | snp | A/G/T | 0.0165278 | 0.0893908 | intron-variant | SAE1 | GRCh38.p7 | 19:47138878 | CAAGTAGCATAATTC[A/G/T]AGATAGAAGAGGATG | 10055 |
rs76340530 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47172778 | ACGCCAAAAAAAAAA[A/G]AGAGAAAAGAAAAAA | 10055 |
rs76402919 | snp | A/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47199411 | AAAAAAAAAAAAAAA[A/G]AAGGCAGCAATAGAG | 10055 |
rs76520059 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47140949 | TGCCTCTCAGGTTCA[A/G]GCGATTCTCCTGCCT | 10055 |
rs76532720 | in-del | -/ATC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47142525 | GTTTGAGCCACCATC[-/ATC]CTCCCTCACCTTAAC | 10055 |
rs76540167 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47189794 | TTTATTTTCTTCCTA[C/T]TAAAGTACTGGTTTA | 10055 |
rs76568906 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SAE1 | GRCh38.p7 | 19:47161395 | AAACAAACACTATCC[A/G]CCTTAAAAACACAAA | 10055 |
rs76616951 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47168338 | TCTCTCTCTGTTTTT[C/T]CTGTCACCCAGGCTG | 10055 |
rs76670280 | snp | A/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47181827 | AATTTTTTTTTTTTT[A/T]AAGACAGAGTCTTGC | 10055 |
rs76673606 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47177087 | CAGAGAATTCTTGGC[A/G]ATCTTAACTTGCTCA | 10055 |
rs76712664 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47172905 | AAGTGCTATTAACAC[C/T]ACCAGCTACAGAGGG | 10055 |
rs76789219 | snp | A/C/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47184236 | TTTTTGTAAAAATTG[A/C/G]CATGTCTTCTGTTTC | 10055 |
rs76941845 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187674 | CTACAGGTGCCTGCC[A/G]CAACACCCGGCTCAT | 10055 |
rs76987767 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47203617 | ATTTCTCCAGATGTC[A/G]TGGTCACAGTTCTGT | 10055 |
rs77020851 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47154858 | ATCACTTTGATTTAT[G/T]GAGAGCAGCTGTGTG | 10055 |
rs77205258 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47186779 | TTTCATTGCAAAGAC[A/G]AAAGCGTGGGCAGGA | 10055 |
rs77231706 | snp | G/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47166969 | GAACTTTTTTTTTTT[G/T]GAGACGGCGTCTCAC | 10055 |
rs77274475 | snp | C/T | 0.00239066 | 0.0344908 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197374 | TTCCTGAGGACTTTG[C/T]CAGGTTGGTGTCAGT | 10055 |
rs77280178 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190714 | GGGGTCAGCTGCTGC[C/T]GCCTTTGCTCCTGCT | 10055 |
rs77436252 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47163265 | CCAAAAAAAAAAAAA[A/G]AAAATTGAAATTATG | 10055 |
rs77549613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47148270 | TGGGTCAAGGATACA[A/G]GGTTAGCCTAGAATG | 10055 |
rs77554348 | snp | A/G/T | 0.00438476 | 0.0466401 | intron-variant | SAE1 | GRCh38.p7 | 19:47134491 | TTAAGTGATGAGAAT[A/G/T]TGCCTCTGGACATAG | 10055 |
rs77555729 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129314 | TTTTTTTTTTTTTTT[A/T]TTAGACGGGAGTCTC | 10055 |
rs77562995 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SAE1 | GRCh38.p7 | 19:47160178 | ACTCAGTTGCCTGGA[C/T]TGGAACCCTCAGGCC | 10055 |
rs77568928 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47153296 | TACAAAATAGTTGGG[C/T]GATTCTGGAGGCATA | 10055 |
rs77650237 | snp | A/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47168202 | GTCTGGAAAAAAAAA[A/T]TGTTTAAAACAAAAA | 10055 |
rs77687751 | snp | A/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47143110 | TTAGAACCAAAATGA[A/T]TTTTTTTTTTTTGAG | 10055 |
rs77734579 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47163252 | GCTTGGAGTACATCC[A/C]AAAAAAAAAAAAGAA | 10055 |
rs77749070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166340 | TAAGGAGTGTGAAAA[C/T]TTCAAATTTGATCCA | 10055 |
rs77776702 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47192055 | CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAGAAA | 10055 |
rs77828218 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47178827 | ATTACATTTGTGCAC[G/T]GAAGCAGGGAGGAAA | 10055 |
rs77871161 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47138817 | TGAGGCCCCATTTCA[A/G]TCAAAACAGTGGGCA | 10055 |
rs78034057 | in-del | -/AAA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163262 | CATCCAAAAAAAAAA[-/AAA]GAAAATTGAAATTAT | 10055 |
rs78056538 | snp | G/T | 0.0341408 | 0.126114 | intron-variant | SAE1 | GRCh38.p7 | 19:47173062 | GAGACAGAGTCTTGC[G/T]CTATCACCCAGGTAG | 10055 |
rs78078676 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47159367 | TCCACTGCTGGTGGC[C/T]CTTAGGTTGCTTGTC | 10055 |
rs78112532 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | SAE1 | GRCh38.p7 | 19:47196675 | CTCTTCCAGGTCTTA[A/G]TAGAGCCTTTTTCCT | 10055 |
rs78138403 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SAE1 | GRCh38.p7 | 19:47145558 | CTCTCTCTACATTCC[C/T]ATGCCTCAGTGACAT | 10055 |
rs78213020 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47152050 | CAAAGGAACACATTT[A/C]TCTGTGAGTGTTATT | 10055 |
rs78313574 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47188350 | CTGAGGCCATGTCTC[A/C]AAAAAAAAAAAGAAA | 10055 |
rs78321286 | snp | G/T | | | intron-variant, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47131091 | TATTCTGAGGCGTTT[G/T]CGGCCCGGAAGGAGC | 10055 |
rs78416546 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47169806 | CTAAGCAGTTCTGCC[C/T]TTTTTCCACAGAAGG | 10055 |
rs78488038 | snp | A/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47168193 | GGGGAGACTGTCTGG[A/G]AAAAAAAAATGTTTA | 10055 |
rs78520932 | snp | C/T | 0.34437 | 0.231505 | intron-variant | SAE1 | GRCh38.p7 | 19:47140940 | TGAAACCTCTGCCTC[C/T]CAGGTTCAAGCGATT | 10055 |
rs78535257 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SAE1 | GRCh38.p7 | 19:47174347 | ATAACATAAAATTTA[C/T]CATTATAACTTAAGC | 10055 |
rs78547115 | snp | A/G | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47199410 | AAAAAAAAAAAAAAA[A/G]AAAGGCAGCAATAGA | 10055 |
rs78548188 | snp | A/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47143109 | GTTAGAACCAAAATG[A/T]TTTTTTTTTTTTTGA | 10055 |
rs78636570 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47162099 | GCATAGCACAGATTA[C/T]ATTCTGTTCCATCAT | 10055 |
rs78654818 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47146489 | TTTAGGTGGTAGAAT[C/T]GGGAGGTCTGTGTAT | 10055 |
rs78717847 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47134981 | TAGACAGTCTTAGAG[A/G]GTTTATTAAAGTGTT | 10055 |
rs78753311 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190527 | GAAAGAGTGAAAAAA[A/G]ACAGCTTCTGTTTGT | 10055 |
rs78826976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47174506 | GGTTTAAGCAATTCT[C/T]CTGCCTCAGCCTTCT | 10055 |
rs78967707 | snp | C/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47172731 | AAACAGAGTCAATCA[C/G]AGATCATCTACTCCA | 10055 |
rs78976141 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47135523 | TCATTCCCTTTTTTT[G/T]GTAGACAGGGTCTCT | 10055 |
rs78977591 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47184778 | GACATGGTTGTGGGG[G/T]TTTTTTTGTTTTTGT | 10055 |
rs79176791 | snp | A/G | 0.00795532 | 0.062565 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210746 | CAGGGGCTGCATTTC[A/G]GAAAGGATCCGTGTC | 10055 |
rs79238875 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | SAE1 | GRCh38.p7 | 19:47205564 | CCCAGAGGACTGTTC[A/G]AGCAGGATTCTGAGG | 10055 |
rs79323067 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47158516 | GAAGTGCCCAAAAAG[A/G]TTTCCCAGAGGAAGA | 10055 |
rs79344001 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | SAE1 | GRCh38.p7 | 19:47135630 | CCACCTCAGCCTCCC[A/G]GTAGTTGTGACTATA | 10055 |
rs79451739 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47135812 | TCTATTTTTTTTTTT[G/T]AAACGGAGTCTCGCC | 10055 |
rs79468712 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190526 | AGAAAGAGTGAAAAA[A/G]GACAGCTTCTGTTTG | 10055 |
rs79543175 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47203556 | TGCTATCTGAATCGG[A/G]CCCTCCTGCTAGAAG | 10055 |
rs79607356 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SAE1 | GRCh38.p7 | 19:47185233 | CATTCTGTCAATATG[C/T]CTTTATATGTGGTAC | 10055 |
rs79689014 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47197450 | TTGCCTTAATTTGAC[A/G]AGCTCTTTTATTAGA | 10055 |
rs79717330 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47168219 | GTTTAAAACAAAAAA[C/T]TGTTTTTTTGTATGT | 10055 |
rs79758356 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | SAE1 | GRCh38.p7 | 19:47173002 | GCCCACTGGAAGCCA[A/G]GTCTGTTTTGATTCC | 10055 |
rs79766856 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47158881 | GATTTACAAAGAGGG[A/T]TACCCCTGAAGTTGC | 10055 |
rs79777780 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47152104 | CAGCAAAGAGGGTCT[A/G]TCAAGTGAAAATGTC | 10055 |
rs79782600 | snp | C/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47142165 | GAGGCAGGTGGATCA[C/G]TTGAGGTCAGGGGTT | 10055 |
rs79805310 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SAE1 | GRCh38.p7 | 19:47153788 | TTTGGGCATATTATT[A/G]TTATTATTATTTTAT | 10055 |
rs80000027 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47138523 | TTTTATTATGTACCA[A/G]ATTTCTATAATTCTG | 10055 |
rs80016906 | snp | A/G | | | splice-acceptor-variant | SAE1 | GRCh38.p7 | 19:47152896 | TTTCTTTCTTTCTGC[A/G]GGTGTGTCTGACTTG | 10055 |
rs80116827 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47198125 | CTCTCTTTTTTTTTT[G/T]TGAGACAGAGTTTTG | 10055 |
rs80165670 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SAE1 | GRCh38.p7 | 19:47186656 | TTTCCCCATCAACAA[C/T]TTTCATCCGGCGCCT | 10055 |
rs80186461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47195705 | TTCGCTTCTTCCTTC[C/T]CTTTGTTCCTTTTCC | 10055 |
rs80310462 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SAE1 | GRCh38.p7 | 19:47206526 | AGATACCCTATTTTA[C/T]ATCCATGTCTACTTC | 10055 |
rs80340314 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47189352 | CACGAGGTCAGGAAT[C/T]TGAGACCAGCCTGAC | 10055 |
rs111298954 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47200761 | TACTCATTTATATAT[C/T]ATCTGTGGCAGCTTT | 10055 |
rs111301108 | snp | C/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47155012 | CTCCAAAGCTTTTGC[C/G]CTTAACCACCATCCC | 10055 |
rs111410846 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47131476 | ACCGGACAGACGGGA[G/T]CTTACACTCTTGTGG | 10055 |
rs111428108 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47156904 | CCATGCGATGGGGAA[A/C]GCAAGATGAAGGGGC | 10055 |
rs111453008 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | SAE1 | GRCh38.p7 | 19:47174795 | AGCCAGGATGGTCTC[A/G]ATGTTCTGACCTCGT | 10055 |
rs111477157 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47177540 | TTTTAAAAAATCTGT[G/T]TGTACAGATTGGGGC | 10055 |
rs111484931 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47141501 | GTAGGAATGTAGGTC[A/G]TGGAGAGCAGATTTA | 10055 |
rs111579621 | snp | C/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47136193 | GCCCAGGCTAGAGGA[C/G]AGTGGCACGATCTCA | 10055 |
rs111593906 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SAE1 | GRCh38.p7 | 19:47167930 | AGGCACAGTGGCTCA[C/T]GCCTATAATCCCAAC | 10055 |
rs111594540 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190440 | AGGGTCAGTTCTGAG[G/T]CTGCTGCCTGTCAAG | 10055 |
rs111596279 | snp | A/T | 0.00416031 | 0.0454186 | missense, utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209252 | CTTGGCCCCAAGTGA[A/T]CTCAAGATTTGGCAG | 10055 |
rs111607782 | in-del | -/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47181399 | TTTCCATGTTATTTA[-/T]TTTTACAGTTATGAT | 10055 |
rs111645298 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47137927 | AGAGACGGGGTTTTA[C/T]CATGTTGGCCAGGCT | 10055 |
rs111648130 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47170300 | GCTCACTGCAACCTC[C/T]ACCTCCTGGGTTGAA | 10055 |
rs111745295 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130754 | CCGGATCGCCTTTGA[A/G]TCTCGTGAGGTACTT | 10055 |
rs111777496 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SAE1 | GRCh38.p7 | 19:47155026 | CCCTTAACCACCATC[C/T]CGATCTGTGACCTGG | 10055 |
rs111827958 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47197047 | TTAGCCAGGCATGGT[G/T]GTTCGTGCCTGTAGT | 10055 |
rs111939631 | snp | A/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47154325 | TGAACTCCTGACCTC[A/T]GGTGGTCCACCCACC | 10055 |
rs111945862 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SAE1 | GRCh38.p7 | 19:47179124 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 10055 |
rs112028400 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47159743 | GTGTCACCCAGGCTG[G/T]AGTGCAGTGGCACAA | 10055 |
rs112037343 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47136417 | TGTTGCAATTACAGG[C/T]GTGAGCCACCACACC | 10055 |
rs112054034 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47146049 | TAAAGAACAAGGAGG[G/T]TTGTCAAGATAAGAG | 10055 |
rs112173329 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47163726 | AGCAAGACTCTATCT[C/G]AAAAATAAATAAATA | 10055 |
rs112208039 | snp | A/C | 0.021333 | 0.101051 | intron-variant | SAE1 | GRCh38.p7 | 19:47199658 | CTCACGGCCCAGCAC[A/C]CAGCCCCAGGTATGC | 10055 |
rs112244309 | in-del | -/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47139125 | CCTGGCTAATTTTTG[-/T]ATTTTGAGTAGAGAT | 10055 |
rs112267778 | in-del | -/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47183089 | TCCGGCTAATTTTTG[-/T]ATTTTTAGTGGAGAT | 10055 |
rs112280226 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47135019 | CATTTTCAGCCGAGG[A/T]TTTTAGAAATTAAAA | 10055 |
rs112297259 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47167946 | GCCTATAATCCCAAC[A/T]CTTTGGGAGACCGAG | 10055 |
rs112430089 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47189111 | TGAATGAACAATTGA[C/T]TGAATGTCAGGCCCA | 10055 |
rs112437143 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | SAE1 | GRCh38.p7 | 19:47175472 | CTGGGCGCGGTGGCT[C/T]ATGCCTGTAATCCCA | 10055 |
rs112522969 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47207220 | ACCTGGGTAGCAGAA[A/C]AAGATCCTATCTCAA | 10055 |
rs112532975 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | SAE1 | GRCh38.p7 | 19:47132428 | GACTAATTTTTGTTT[G/T]TTTTTTTTTTTGTAG | 10055 |
rs112541679 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47198617 | CAGGTATCATTACAG[G/T]GCTTGCTCTAGTAGC | 10055 |
rs112622440 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47177296 | ACAAATAATTCTACT[C/T]CTTGTGAGGACAGCT | 10055 |
rs112788625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161098 | CCTTGAACTCCTGGG[A/C]TAAAGGGATCCTCCC | 10055 |
rs112893094 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47167784 | CTTTTTAAAATATAG[A/G]GACACAGAGTCTATA | 10055 |
rs112953047 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47205499 | ACATAGCCCAGAGTG[A/C]TGTGAAAATTACAGT | 10055 |
rs112999402 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47184753 | AGAGCTCAGTCTGAA[A/T]GTAGGATATGACATG | 10055 |
rs113051385 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47149186 | TTTTTTTTTTTTTTT[C/T]TTGAGACGGAGTCTT | 10055 |
rs113084645 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155708 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 10055 |
rs113088983 | snp | A/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47140675 | GTGGTGTGCACCTAT[A/T]GTCCCAGGACTCAAT | 10055 |
rs113092444 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47172807 | AAAGCACATATCTTC[A/G]CGGATGACAGAGTTC | 10055 |
rs113097500 | snp | C/T | 0 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47194764 | TTTTTTTTTTTTTTT[C/T]TTTGAGATGGAGTTA | 10055 |
rs113149127 | in-del | -/TGTG | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47182480 | GTGTGTGTGTGTGTG[-/TGTG]TGTGTGTGTGTGTGC | 10055 |
rs113275493 | snp | G/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47151905 | GGCCGTGTTTGGCTG[G/T]TCCTTGCAGGTTTTA | 10055 |
rs113278365 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SAE1 | GRCh38.p7 | 19:47175821 | TTAGGGAAACAGGAT[C/G]ACCACCATAGTAGAA | 10055 |
rs113294745 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191294 | TGGGCGTCTCCAGCC[C/T]GGGTGACAGAGTGAG | 10055 |
rs113345964 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47164343 | CCGGCTAATTTTTTG[C/T]ATTTTTAGTAGAGAC | 10055 |
rs113372028 | in-del | -/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47148985 | TTTGCACAAGTTTGA[-/T]TTTTTTTTTTAAGTT | 10055 |
rs113444815 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47202507 | GGGCCAGGATGATCT[C/T]GATCTCTTGACTTTG | 10055 |
rs113456709 | snp | A/G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47196384 | ATTTTACTTTTTTGA[A/G/T]ACGGAGTCTCACTCT | 10055 |
rs113477004 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47173967 | TTTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC | 10055 |
rs113478474 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47194765 | TTTTTTTTTTTTTTT[C/T]TTGAGATGGAGTTAC | 10055 |
rs113578728 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47201465 | CAACCTCTGCCTCCC[A/G]GCTTTAAGTGATTCT | 10055 |
rs113647550 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47147282 | CATGATCATGGCTCA[C/T]TGTAGCCTTAACTTC | 10055 |
rs113659212 | snp | A/G | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209927 | TACCAAGTCTTGGAT[A/G]TTAGGGCGAGACCCT | 10055 |
rs113697795 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47171239 | CAGCCCCCCAAAGTG[C/T]TGTGATTACAGGTGT | 10055 |
rs113716296 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SAE1 | GRCh38.p7 | 19:47174548 | ATTACAGGCATATGT[C/T]ACCACGCCTGGCAAA | 10055 |
rs113787280 | snp | A/G | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47154822 | TTTATTTCATGATTC[A/G]AGTAGAGTGTTTACA | 10055 |
rs113852155 | in-del | -/A | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47163808 | TATTTATTTAGAGAC[-/A]AGAGTCTTGCTTTAT | 10055 |
rs113868403 | snp | A/C | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47189547 | GCCTGGGTGACAGAG[A/C]GAGACTCTGTCTTAA | 10055 |
rs113907035 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47136822 | GCAGCTCTCTGGAGT[C/T]GGAAGGGCAGTGATT | 10055 |
rs113966999 | snp | C/T | 0.5 | 0 | intron-variant | SAE1 | GRCh38.p7 | 19:47209136 | GCACTTGAGCTAAAC[C/T]CTCTTTTCATTTTTC | 10055 |
rs113986489 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150211 | TCCTAGGTAACTCCA[A/G]AAGATCCCGGAGCTC | 10055 |
rs114004266 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47141686 | AGGAAGAAATGGTGC[A/G]TTTTGCGAGGGTGGA | 10055 |
rs114005876 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47183730 | AGCCTCACATCTTTT[A/C]TCTGACTGTCAGACA | 10055 |
rs114032036 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47198615 | CCCAGGTATCATTAC[A/G]GTGCTTGCTCTAGTA | 10055 |
rs114133304 | snp | C/T | 0.030665 | 0.119967 | intron-variant | SAE1 | GRCh38.p7 | 19:47156440 | GCCGAGACGGCAACA[C/T]TGCACTCCAGCCTGG | 10055 |
rs114251100 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47174081 | GAGCCACTTCGCCCA[A/G]CCTGTTTACCCTTAA | 10055 |
rs114262203 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47148080 | CTGTACGTTTTTATC[C/T]ATGTCCTCGTTTTAT | 10055 |
rs114323480 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47194165 | AGAGACCAAGATTCA[C/T]TCACTCGCCATTGGA | 10055 |
rs114379617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191489 | GAAAGGGTATCAACA[C/G]TGCCTGAGCAGATGG | 10055 |
rs114448664 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47136394 | TGGCCCTCCTTGGCC[C/T]CCCAAAGTGTTGCAA | 10055 |
rs114451215 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47206660 | GTTCATGGTAAAACA[C/T]ATACCATCTCCTGTA | 10055 |
rs114482326 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47166202 | GGTGAGAAAGGATGA[A/G]CTGGGTAGCTACACT | 10055 |
rs114485014 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SAE1 | GRCh38.p7 | 19:47169309 | GGAGTGCAGTGACGC[A/G]ATCTTGGCTCGCTGC | 10055 |
rs114679610 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47205034 | AAAACTATACCATAC[A/C]CCCAAATATATTGTA | 10055 |
rs114696011 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47188210 | AAAATGAACCACCAG[C/G]CATGGTGGTGCATGC | 10055 |
rs114770152 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47163845 | GGCTGGAGCGCAGTG[A/G]CGTGATCTCCGTCTC | 10055 |
rs114896388 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47148089 | TTTATCCATGTCCTC[A/G]TTTTATATGGGATTC | 10055 |
rs114910415 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47161580 | TTCCTGTTTTATCAC[A/G]TGTTTATAAATCTAA | 10055 |
rs114967410 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | SAE1 | GRCh38.p7 | 19:47177362 | CCTGGTTTTTGTTTG[G/T]TTTTTTTCCCCCCCA | 10055 |
rs115089680 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47163096 | AAATGATAACTATAA[C/T]CTTCCTTTCAGTATT | 10055 |
rs115094772 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47199578 | GGCCTTCAACTCTGC[C/T]GGCCGGTGATGCAGA | 10055 |
rs115157253 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47203554 | ACTGCTATCTGAATC[A/G]GGCCCTCCTGCTAGA | 10055 |
rs115211627 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SAE1 | GRCh38.p7 | 19:47132371 | TTCCCTCTTCAGCCT[C/G]CCAAGTAGCTGGGAC | 10055 |
rs115213951 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SAE1 | GRCh38.p7 | 19:47175155 | TAAAGTCAAGCCTCA[A/G]TAACATTCTGATTTC | 10055 |
rs115405598 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47177423 | GAGTGTGGTGGCACA[A/G]TCATAACTCACTATA | 10055 |
rs115413517 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47176044 | TTTCTAGGAGAACTA[C/T]TGTTAAGTTTTTTAG | 10055 |
rs115419969 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47161301 | TAGGCATGAGCCACC[A/G]TACCCAGCCTATATT | 10055 |
rs115428385 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47135584 | ATCACAACTCACTTC[A/C]GCCTTGACTTCTTGG | 10055 |
rs115455465 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SAE1 | GRCh38.p7 | 19:47132580 | CCATGCCTGGCCTCA[C/T]TGATCAATATTTTTA | 10055 |
rs115635670 | snp | G/T | 0.00132288 | 0.0256844 | intron-variant | SAE1 | GRCh38.p7 | 19:47180143 | CACGTGTTTATTTCC[G/T]AGAATTGTTTCCTAG | 10055 |
rs115828525 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47133113 | GCATGATTGTCAAAT[A/T]AGAGAAATAAGGTGG | 10055 |
rs115860558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47143771 | ATTGTTGGGTTTGAA[C/T]TCTAGCTCCACCACA | 10055 |
rs115959398 | snp | C/G | 0.0333238 | 0.124705 | intron-variant | SAE1 | GRCh38.p7 | 19:47187960 | CAGGTGTTCAGTATA[C/G]AGTAGTGACATCGCC | 10055 |
rs116021796 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | SAE1 | GRCh38.p7 | 19:47168511 | GTTGCCCAGGCTGTT[A/C]TTTGACTCCTGGACT | 10055 |
rs116023478 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47152492 | AAACATGACCTTTGG[G/T]TCAATTTAAAAAACT | 10055 |
rs116075123 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47172358 | GTGGAAGAGGCACCA[A/G]CAGTAAGAGCAGAGT | 10055 |
rs116131054 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SAE1 | GRCh38.p7 | 19:47162862 | CTGGGCGTGGTAGCA[C/T]GTGCCAGTGGTCTCA | 10055 |
rs116303596 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176823 | TCGCCATCTGTGAGC[A/G]AAAGGTCTCTTCTTT | 10055 |
rs116347725 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210980 | CTCTAACGGCAGAGA[C/T]TAAGTCACCCAGAGG | 10055 |
rs116413011 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47131483 | AGACGGGAGCTTACA[C/T]TCTTGTGGGAGCTCA | 10055 |
rs116467952 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SAE1 | GRCh38.p7 | 19:47184756 | GCTCAGTCTGAATGT[A/G]GGATATGACATGGTT | 10055 |
rs116476287 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47189677 | AAAAGCTTTGGGCCT[C/G]TCTCAGGTAAATGAA | 10055 |
rs116534371 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47172012 | GCAACCTCCACCTCC[C/T]GGTTCAAACAGTTTC | 10055 |
rs116558259 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47194606 | GGAGAAAGAGTATTG[A/T]CCTTAGAGACAAGGC | 10055 |
rs116589235 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47156133 | AAAAATTTGTCTGGC[A/G]TGATGGTGAGCACCT | 10055 |
rs116640747 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47198554 | GTTTACTGAGCAGCT[A/G]TTATGTACTAGGCAT | 10055 |
rs116651172 | snp | G/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47130791 | CCAGGCTCCGCGGAC[G/T]AGGTACTGCGCAGGC | 10055 |
rs116732633 | snp | C/T | 0.0333695 | 0.124785 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191154 | AGTGGGTCATGCCTA[C/T]AATCCCAGCACTTTG | 10055 |
rs116760620 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SAE1 | GRCh38.p7 | 19:47159578 | TTTCTTTGAAGCAGG[A/G]TCTGACTACTCTGTC | 10055 |
rs116816520 | snp | A/G | 0.0252325 | 0.109451 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210349 | AGCAAGAGTTAAATT[A/G]TTCACATTCTAGAAT | 10055 |
rs116921808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186652 | TCCTTTTCCCCATCA[A/G]CAACTTTCATCCGGC | 10055 |
rs116980988 | snp | A/T | 0.207864 | 0.246424 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47128827 | TTTATTTATTTATTT[A/T]TTTTTTTCTGAGACG | 10055 |
rs117029094 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SAE1 | GRCh38.p7 | 19:47206797 | TTATTAATAGCAGCT[C/T]CTACTTACTAAGAAT | 10055 |
rs117068689 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47143955 | TGAAAATGCAGAGTG[G/T]CCTGGAGGCTTCGTG | 10055 |
rs117171492 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SAE1 | GRCh38.p7 | 19:47173363 | TAGCTACTGTTTCTT[C/T]CTCAACCACCTGTCC | 10055 |
rs117180804 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SAE1 | GRCh38.p7 | 19:47135111 | ACAGGCATACAATGG[A/G]TAATAATCACATCAG | 10055 |
rs117181234 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47183820 | CAGATGCCTAGAGTC[A/G]AGGTCATGTGCTGCT | 10055 |
rs117189561 | snp | G/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209861 | TGCTGTTCTTGAGTT[G/T]TCGTTTAGGATTAGT | 10055 |
rs117201178 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SAE1 | GRCh38.p7 | 19:47185067 | TCGGGTGATCCACCC[G/T]CCTCGGCCTTCCAAG | 10055 |
rs117229552 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47190012 | TCCACAGTTTTTTCT[A/G]TAAATAACGTGAAAC | 10055 |
rs117259389 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47158704 | AATGCCTACTGTGTG[C/T]AAGGCACTGTGTTGA | 10055 |
rs117362995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47202586 | CCACTGAGCCCGCCC[C/T]AATTATACCCGTTTA | 10055 |
rs117436118 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | SAE1 | GRCh38.p7 | 19:47178221 | GCACTCCAGCCTGAC[A/G]ACAGGGCAAGACTCC | 10055 |
rs117484618 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47192655 | TCAAGCAATTCTACT[G/T]CCTCAGCCTCCCAAG | 10055 |
rs117516426 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | SAE1 | GRCh38.p7 | 19:47157720 | CTACGTGGAGCTGAG[C/T]TGGAAGGTATCAAAA | 10055 |
rs117605411 | snp | C/T | 0.0100805 | 0.0702753 | intron-variant, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197285 | CAGTTCTGATACATA[C/T]GAGGAAGATTCTGAG | 10055 |
rs117606121 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | SAE1 | GRCh38.p7 | 19:47159534 | TAATCCAGCAACCCT[A/G]GAGATTATTTTCTTC | 10055 |
rs117606416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150835 | ACCTGATCTTGATCT[A/G]TGTCTGTCTGTCTGT | 10055 |
rs117637056 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47184208 | TAGGGGAGCCAAATC[C/T]ATTTTAAAGTGATTT | 10055 |
rs117728897 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47172843 | GACTTGCTCTGTGCC[A/G]GGCGTTTTCCATGTA | 10055 |
rs117780807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47132055 | CAGCCTCTGGCCTCC[C/T]GGGTTCAAGACTTCC | 10055 |
rs117788309 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SAE1 | GRCh38.p7 | 19:47156231 | AGCCATGGTCACACC[A/G]CTGCACCCCAACCTG | 10055 |
rs117960763 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | SAE1 | GRCh38.p7 | 19:47132733 | CTCTACAAAAAAATA[C/G]AAAAATTAGCCAGGC | 10055 |
rs117988750 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SAE1 | GRCh38.p7 | 19:47203901 | CCATTTTCTCTGGCC[C/T]ATCCAGGTGCCATTC | 10055 |
rs118004379 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47139406 | GCCCAGGCTGGTTTC[A/G]AACTCATGGGCTCAA | 10055 |
rs118029635 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SAE1 | GRCh38.p7 | 19:47198584 | TCAGGTAGTAAGTAG[A/C]CAACCCAGATCCCAC | 10055 |
rs118081969 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | SAE1 | GRCh38.p7 | 19:47158812 | CAAGGCCACACAGCT[A/G]TGGAAGAAGGGGCGA | 10055 |
rs118118032 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | SAE1 | GRCh38.p7 | 19:47169529 | GGATTACAGGTGTGA[C/T]CCACCGCGCCTGGCC | 10055 |
rs118175860 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47133055 | CATCTGGGAGAACTT[C/T]CCTAGCTAAGAGAAC | 10055 |
rs137870485 | snp | C/T | 3.29489e-05 | 0.00405874 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143587 | AGTGAAAGGACTGAC[C/T]ATGCTGGATCACGAA | 10055 |
rs137903335 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SAE1 | GRCh38.p7 | 19:47174603 | TGTGAGACGGAGTCT[C/T]GCTCTGTCTCCCAGC | 10055 |
rs137971970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47184357 | AGTTTTCCTACCACT[A/G]AAATGGGGGTGGTAA | 10055 |
rs137986243 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | SAE1 | GRCh38.p7 | 19:47165014 | CTGGTCTCGAACTCC[A/T]GACCTTGTGATCCAC | 10055 |
rs138012905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47156098 | ACAGTAGCAAGACCC[C/T]GTGTCTACAAAAAAA | 10055 |
rs138040531 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47197612 | TGGTTCAAAATTCAA[A/G]GCAATGTAAGATCTG | 10055 |
rs138103448 | snp | G/T | 4.94197e-05 | 0.00497066 | missense, nc-transcript-variant, utr-variant-5-prime | SAE1 | GRCh38.p7 | 19:47143562 | TTGCCAAGAATCTCA[G/T]CTTGGCAGGAGTGAA | 10055 |
rs138107720 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47161507 | ACCCCAGAGCTGCTG[A/G]TACATTTGTGTGGAT | 10055 |
rs138124511 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47168289 | TGATGCCACATGTGT[A/C]ATTTCCAAATATTTC | 10055 |
rs138126493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152128 | AAATGTCCTTTTGTT[C/T]AGGAGAAAGCATGTG | 10055 |
rs138136331 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47137730 | GTGTGTGTGTGTGTT[G/T]TTTTTTTTTTTTTTT | 10055 |
rs138150039 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129515 | GGCCGGGCTGGTCTC[A/G]AACTCCTGACTTCGT | 10055 |
rs138171546 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | SAE1 | GRCh38.p7 | 19:47198403 | AGGCATGAGCCACCA[C/T]GCGCTCCATCCACAT | 10055 |
rs138256416 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47173974 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGCGT | 10055 |
rs138256634 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47204140 | ACCTGTGCTCTTAAC[C/G]TCTGTACAGTTTATC | 10055 |
rs138256884 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47157926 | GACTGGGTTTTGGCC[A/G]TGGCTTTGTCACCTT | 10055 |
rs138323329 | in-del | -/TC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186828 | GGCATTTCAGAGTAG[-/TC]TCTTCATGGGCGGCC | 10055 |
rs138389701 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47136456 | TTTATTTTCATTTGG[A/G]TATATACCTAGCAGT | 10055 |
rs138416958 | in-del | -/AAAGA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193842 | AAAAAAAAAAAAAAG[-/AAAGA]AAAGAAAAAGAAAAA | 10055 |
rs138430318 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47148690 | CACGACCTGGGCTCA[A/C]TGCAGCGTCTGCCTC | 10055 |
rs138453601 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47204510 | GCCGCACCCCCCCCC[C/T]TTTTTTTTTTTTTTG | 10055 |
rs138478703 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47143262 | AGGCGCCTGCCACTA[C/T]GCCCAGCTAGTTTTT | 10055 |
rs138483378 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47134257 | TGTGTGAGTACAGAG[C/T]ATAGAATTAATGGAG | 10055 |
rs138515083 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47179244 | GTCGCGATGGCTCAC[A/G]CCTGTAATCCTAGCA | 10055 |
rs138532513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182430 | ATGACCACAGATGTT[C/T]AAAAATAATTTGTAA | 10055 |
rs138590069 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47160844 | AATCCTGCTAATTAT[C/T]AATATCAGAACTACT | 10055 |
rs138693550 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SAE1 | GRCh38.p7 | 19:47208782 | GACTGGTCTTGAATT[C/T]CTGGGCTCAAGTGAT | 10055 |
rs138725625 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47165366 | AAGTGCTGGGATTAT[A/G]GGTGTGAGCCACCGC | 10055 |
rs138745969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194397 | ACCTTAATTTTTATG[C/T]AGGAACCCTTGTCCT | 10055 |
rs138748365 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SAE1 | GRCh38.p7 | 19:47198143 | AGACAGAGTTTTGCT[C/T]TTGTTGCCCAGGCTG | 10055 |
rs138762781 | snp | A/C/G | 0.000428523 | 0.0146316 | missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209164 | TTCTCCCCAGGCCCT[A/C/G]TCTCAGCGGGACCCT | 10055 |
rs138869054 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SAE1 | GRCh38.p7 | 19:47189492 | CTTGCACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 10055 |
rs138872831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47137687 | GTGCATGGCGTATGC[C/T]GTAACACTCAGCTGA | 10055 |
rs138998654 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47133438 | CACCATGTTAGACAG[A/G]ATAGTCTCGATCTCC | 10055 |
rs139043112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171505 | CTGTTGCCCAGGAGA[G/T]CAGTGGCGTGATCTT | 10055 |
rs139060088 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47131278 | TGGGGAGTCCTGAGA[C/G/T]AGCGGGAGAATTCAA | 10055 |
rs139139711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47173052 | TTTTTCCCCAGAGAC[A/G]GAGTCTTGCTCTATC | 10055 |
rs139190486 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190977 | CCCTGTATGGACCTG[C/G]TGTTTCTTTTGGATT | 10055 |
rs139253941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170018 | TTTTGTGATGTTTGC[C/T]TTGGGTGGCATTCTT | 10055 |
rs139413477 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SAE1 | GRCh38.p7 | 19:47202169 | TTAAGGAATTATTTC[A/G]ACGCCTGTGTCTTTG | 10055 |
rs139485188 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SAE1 | GRCh38.p7 | 19:47167364 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTG | 10055 |
rs139486747 | snp | A/G | 0.00397017 | 0.044377 | intron-variant | SAE1 | GRCh38.p7 | 19:47153062 | GTTGGGAGAGGAGGG[A/G]AGAACATAACATTTT | 10055 |
rs139505036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206361 | CAGCCAGCTGGCAGG[C/T]GGGGCCTGCAGTCCA | 10055 |
rs139606633 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47149840 | CTCAGCACTTTGGGA[A/G]GCTGAGGCAGGCGGA | 10055 |
rs139606797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194888 | CCTGGGACTACAGGC[A/G]TGCGCCACCACGCCT | 10055 |
rs139611996 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47152745 | AACTTTTCTTTTGTC[G/T]TCTAGCCATAGGGCC | 10055 |
rs139631620 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47149210 | GAGTCTTGCTCTGTT[A/G]CCCAGGCTGGAGTAC | 10055 |
rs139721071 | in-del | -/AAAAGA | | | intron-variant | SAE1 | GRCh38.p7 | 19:47193846 | AAAAAAAAAAGAAAG[-/AAAAGA]AAAAGAAAAAGAAAT | 10055 |
rs139730625 | snp | C/T | | | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191727 | TTTTTTCAGCTGTTA[C/T]CACAAAGCTTTTCAT | 10055 |
rs139748473 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47145152 | GGATTACAGGCATGC[A/C]ACACCATGCCTGGCT | 10055 |
rs139769065 | in-del | -/AG | | | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210732 | CGCCGGAGGTGAGAC[-/AG]GGGCTGCATTTCGGA | 10055 |
rs139794298 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47186899 | CTGTGTGGCTGTGGC[A/G]ACAGACAGAGGCTTA | 10055 |
rs139799872 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SAE1 | GRCh38.p7 | 19:47135299 | TATATTTTTGTATCC[A/G]TTAGTCATCCCTCCT | 10055 |
rs139802996 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152966 | TCACAAAAATAGCAT[C/G]AAGTTCTTTACAGGA | 10055 |
rs139818565 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SAE1 | GRCh38.p7 | 19:47138244 | AGACCAGGTTTCGCC[A/G]TGTTGGCCAGGGTGG | 10055 |
rs139858397 | snp | A/G | 0.000798403 | 0.0199641 | SAE1 | 19 | allele_origin=G(germline)/A(somatic) | 19:47175005 | TGAGGCACCGTGCCC[A/G]GCAGTGAGAACATTT | 10055 |
rs139928270 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200223 | CAAGTGTGAGCCACC[A/G]CGCCCAGCCTCTTTT | 10055 |
rs139943015 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47171710 | CTCAGGTGATCTGCC[C/T]ACCTCAGTCTCCCAA | 10055 |
rs140036621 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SAE1 | GRCh38.p7 | 19:47205912 | CTGTCCTCTTCACCA[C/T]GGGGCAGTCATGCAT | 10055 |
rs140068662 | snp | C/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158575 | GCTTTCCAGGCACCA[C/G]AGCCAAGAGCAGTGC | 10055 |
rs140118489 | snp | A/G | 0.000164718 | 0.00907368 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155163 | GTAGAAGATGGGCCC[A/G]ACACCAAGAGAGCAA | 10055 |
rs140153864 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47153952 | ATGCGTCACCATGCC[C/T]GGCTAATTTTGTATT | 10055 |
rs140317552 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47132609 | TACTTAGCCTGGACG[C/T]AGTGACTCACACCTG | 10055 |
rs140325538 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SAE1 | GRCh38.p7 | 19:47164447 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGTCT | 10055 |
rs140335066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47207864 | TGGTCTCGAACTCCT[A/G]GGCTCAAGTGATTCT | 10055 |
rs140423012 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47181107 | GGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG | 10055 |
rs140430180 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47202865 | CAGTAAGCCAAGATC[A/G]CGCCACTGCACTCCA | 10055 |
rs140461532 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SAE1 | GRCh38.p7 | 19:47168204 | CTGGAAAAAAAAAAT[A/G]TTTAAAACAAAAAAC | 10055 |
rs140530433 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47143072 | TCTCTTTCCTAGATT[C/G]GAGGTGTGATGCCTC | 10055 |
rs140614276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47155062 | CTTTTTTTGATTCCA[A/G]TAACATGATTCCTAG | 10055 |
rs140623969 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47179926 | TTCTTCTAAGATTGA[C/G]CAGATAGGTAAGTAT | 10055 |
rs140644469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47187834 | GCCTCTGGATTGCCC[A/G]GCCTGTGTCACTTTG | 10055 |
rs140690494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47146714 | AGTAGTTAGTGGTAC[A/G]GCCGGGACCCAGGCA | 10055 |
rs140730571 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47181863 | GGCTGTAGTGCAGTG[A/G]TATGATCACAGCTTG | 10055 |
rs140785718 | snp | A/C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47160370 | GGAACTACAGGTGCG[A/C/T]GCCACCACGCCCAGC | 10055 |
rs140846538 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47202529 | TTGACTTTGTGATCC[A/G]CCCACCTCGACCTCC | 10055 |
rs140891634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166670 | GGTAATTTTTGAAAC[C/T]TGCCTGGTAATACTG | 10055 |
rs140912079 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SAE1 | GRCh38.p7 | 19:47145495 | AGAGCCCAACTCCAA[C/T]GTAGCTTTCTCTGAC | 10055 |
rs140930585 | snp | C/G | 0.000164723 | 0.00907383 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169871 | GGACTGGAGCAGTGA[C/G]AAAGCAAAGGCTGCT | 10055 |
rs140954935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47208385 | CCACCTCAGCCTCCC[A/G]AGTAGCTGGCACCTT | 10055 |
rs140962050 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47132757 | GCCAGGCATGGTGAC[A/G]TAAGTTTATAGTCCC | 10055 |
rs141009085 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SAE1 | GRCh38.p7 | 19:47164237 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 10055 |
rs141049880 | in-del | -/T | 0.072112 | 0.175658 | intron-variant | SAE1 | GRCh38.p7 | 19:47197421 | TCTGGACAGATAAAG[-/T]TTGTTTTCAGGATTT | 10055 |
rs141083994 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47155982 | TTGACCTCGTGGTCC[A/G]CCTGCCTCAGCCCCA | 10055 |
rs141109015 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | SAE1 | GRCh38.p7 | 19:47191823 | CACTTTGGGAGGCCA[A/G]GGCGGGCCGATCACA | 10055 |
rs141124777 | snp | C/T | 4.94262e-05 | 0.00497098 | synonymous-codon, utr-variant-3-prime, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209181 | CTCAGCGGGACCCTC[C/T]TCACAACAACTTCTT | 10055 |
rs141134571 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | SAE1 | GRCh38.p7 | 19:47165120 | ACGGAGTCTTGCTCT[C/G]TTGCCCAGGCTGGAG | 10055 |
rs141145672 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47183512 | ACTTCACAGGCACCT[C/T]GTGACATTTTCTTAT | 10055 |
rs141176827 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47159798 | TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 10055 |
rs141252780 | snp | C/G | 1.64857e-05 | 0.00287099 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197361 | AGTCCTGACCTGCTT[C/G]CTGAGGACTTTGTCA | 10055 |
rs141328358 | snp | A/G | 0.00578039 | 0.0534489 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150210 | TTCCTAGGTAACTCC[A/G]GAAGATCCCGGAGCT | 10055 |
rs141368277 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47192540 | GCATCAGCCACCATG[C/T]CCGGCTACTTAATTT | 10055 |
rs141373281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157183 | AGTAGTTTGGTGCTG[C/T]AAGTGTGATACAGAG | 10055 |
rs141444693 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47147956 | TAGTAGAGATGGGGT[C/T]TCACCGTATTAGCCA | 10055 |
rs141449771 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47204437 | TCTCCTGACATCGTG[A/T]TCTGCCCACCTCAGC | 10055 |
rs141469111 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47163687 | AGCCAAGATCGCACC[A/G]TTGCACTCCAGCCTG | 10055 |
rs141500199 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47136170 | TTGAGACCGAGCCTC[A/G]CTCTGTTGCCCAGGC | 10055 |
rs141562737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143394 | ACAGGCATGAGCCAC[C/T]GTGCCTGGCAAACCA | 10055 |
rs141590831 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47141421 | TGCTGGGATTACAGG[C/T]ATGAGTCACCGGGCC | 10055 |
rs141623683 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47148316 | CATTTTCTTGGAGGA[G/T]AAGGTAGTAAGATAG | 10055 |
rs141668938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177268 | TAAGTGTTCTTGCCA[A/G]TGTGAAAGACAAACA | 10055 |
rs141786638 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173557 | TTCCTCACTTCAGCA[A/C/T]ACTACTGACATTCTG | 10055 |
rs141789275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47194319 | GTGTGACTCTGATGC[C/T]TCAGTCTGGGGTGGG | 10055 |
rs141948719 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SAE1 | GRCh38.p7 | 19:47192258 | GTTGTTGTTGTCGTC[A/G]TTGTTGTTTTGAGAC | 10055 |
rs141957345 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47194421 | TTGTCCTGGTAGAGA[G/T]TATAATTTGCTGAAT | 10055 |
rs141980506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47170569 | TGGAATGCAGTAGCG[C/T]TATCATGGTTCACTG | 10055 |
rs141987360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47198212 | CCGCCTGGGTCCAAG[C/T]GATTCTCCTAACTCA | 10055 |
rs141987796 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47196633 | TCCCAAAGTGCTGGG[G/T]TTACAGCTGTGAGCC | 10055 |
rs142097845 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47175369 | CCGAAAGTCATATCC[A/G/T]TGGTTTTATAGACAG | 10055 |
rs142100275 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47207414 | CATGAATGATGGGAC[A/G]GTGCTCCTGGGAACC | 10055 |
rs142119470 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47164389 | AGCTAGGATGGTCTC[A/C/G]ATCTGCTGACCTCGT | 10055 |
rs142165624 | in-del | -/A | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158281 | GTTTTCACACCCTCT[-/A]AGGAAGCTGGTGGGC | 10055 |
rs142321047 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47172563 | ACAAAAATTAGCCGG[A/T]TGAGGTGGTGTGCGC | 10055 |
rs142347692 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47174612 | GAGTCTCGCTCTGTC[G/T]CCCAGCCTGGAGTGC | 10055 |
rs142388056 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153029 | CAATCTAGGAGAGCA[G/T]GAGTTTGTAGAGTAA | 10055 |
rs142392211 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47154043 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 10055 |
rs142394718 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47158649 | AGAGTTGCTGTGGCT[-/G]GCCCTCACTGCCGCA | 10055 |
rs142423847 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47200425 | TTTTTTTTTTTTTTG[G/T]ATTGACAGGGTCTCA | 10055 |
rs142477356 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47196041 | ACTCTGCCTCTTCCG[G/T]GTCTTTTTTTTTTTT | 10055 |
rs142585450 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SAE1 | GRCh38.p7 | 19:47202296 | TACCTATTTATTTAT[A/T]TATTTATTTTTTGAG | 10055 |
rs142615650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47179560 | TTAGTAGGGATTTTG[A/T]TTTCAGATGAGGTCT | 10055 |
rs142635049 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47140155 | TCTGTTGCCCAGGAT[A/G]GAATGCAGTGGCGCC | 10055 |
rs142758951 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157961 | TAACATGCCTCCTTC[A/C/T]GTTTTGGCACAGATG | 10055 |
rs142762441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151642 | CTGTTCAAATATGGG[C/T]TTGGAAGGATGGATC | 10055 |
rs142772829 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SAE1 | GRCh38.p7 | 19:47186672 | TTTCATCCGGCGCCT[C/G]GGAACCTCTTCAGTA | 10055 |
rs142802488 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47190029 | AAATAACGTGAAACC[A/G]TGCTTGGTTTCTCTT | 10055 |
rs142823267 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47148820 | GGTTTCACCATGTTG[C/G]TCAGGCTGGTTTTGA | 10055 |
rs142826533 | in-del | -/C | | | intron-variant | SAE1 | GRCh38.p7 | 19:47187179 | ATGCCGTGAATGGTT[-/C]AGAGGCCAGGAGAGC | 10055 |
rs142860430 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47199500 | GGGCAGGGAAGGAAC[C/T]ACTTTGGAGAGAAAA | 10055 |
rs142976095 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47130826 | GAGGGTCTGCGCATG[C/T]GCAGAAGCACTCCGG | 10055 |
rs142978913 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | SAE1 | GRCh38.p7 | 19:47159735 | GTCTTGCTGTGTCAC[A/C]CAGGCTGGAGTGCAG | 10055 |
rs143017313 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SAE1 | GRCh38.p7 | 19:47151202 | TCGCCCAGGCTGGAG[C/T]GCAATTGTGCGATCT | 10055 |
rs143123971 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47156708 | ATTTTTAGTAGAGAT[A/G]GGGTTCCACCATGTT | 10055 |
rs143211838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47197730 | TTTTCCACAGCTCCT[C/T]AGTATTCTAGAGTGT | 10055 |
rs143274777 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47135360 | CTCTGGTAACCCTCA[G/T]TCTACTATCTGCATG | 10055 |
rs143276305 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47142971 | TCACCGCCTTATTTC[C/T]ACACCATAGAAGGAT | 10055 |
rs143302961 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47204316 | CATTCTCCTACCTTA[A/G]CCTTCCAAGTAGCTG | 10055 |
rs143320735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47166862 | AAAGATTTGAGGGCA[A/G]TGAAAACATCTTGTA | 10055 |
rs143321323 | in-del | -/GTGC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47182496 | TGTGTGTGTGTGTGT[-/GTGC]GCGCGCACGCACGCG | 10055 |
rs143334468 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47181586 | TAGGTTTACGCCATT[C/T]TCCTGCCTCCCCCTC | 10055 |
rs143354940 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47171720 | CTGCCCACCTCAGTC[C/T]CCCAAAGTGTTGGGA | 10055 |
rs143417482 | in-del | -/GAGGG | 0.0345262 | 0.126772 | intron-variant | SAE1 | GRCh38.p7 | 19:47154459 | AAGCTGCCCACAGCA[-/GAGGG]GCAGAATTAAGTTTG | 10055 |
rs143438077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188412 | AAGGGAAAAAACTGT[G/T]CTGGGAGTGAATGTC | 10055 |
rs143461342 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47181830 | TTTTTTTTTTTTTAA[A/G]ACAGAGTCTTGCTCT | 10055 |
rs143590449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171972 | TCACCCAGGCTGGAG[C/T]GCAGTGGTGCAATCT | 10055 |
rs143609299 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47132615 | GCCTGGACGCAGTGA[C/T]TCACACCTGTAATCC | 10055 |
rs143620389 | snp | A/C/T | 0.0103417 | 0.0712888 | intron-variant | SAE1 | GRCh38.p7 | 19:47152311 | CACCAGTTCATTGTC[A/C/T]AAGCCTGAATGGAAG | 10055 |
rs143669128 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47187000 | GGGTCCCCACCACAG[A/C]TAGCATAGGGTAGGG | 10055 |
rs143684731 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47177426 | TGTGGTGGCACAATC[A/G]TAACTCACTATAGCC | 10055 |
rs143736412 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47166068 | TGGGACCCCTGAAAT[A/C]TCCTGCCCAGACAAC | 10055 |
rs143919871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144432 | AGGCCAGGCACAGTG[G/T]CTCATGCCTGTAATC | 10055 |
rs143925583 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47168496 | TTGGGGTCTCACTTT[A/G]TTGCCCAGGCTGTTA | 10055 |
rs143946727 | in-del | -/CAT | 0.409721 | 0.192325 | intron-variant | SAE1 | GRCh38.p7 | 19:47142521 | GCTAGTTTGAGCCAC[-/CAT]CATCCTCCCTCACCT | 10055 |
rs143990089 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47210055 | ATGCGGCTCAAGTCA[C/T]TCAGAGGCTGTTGCA | 10055 |
rs144025676 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47167533 | GTGTGAGCCACTGCG[C/T]CCAGCCAACAATTTG | 10055 |
rs144033004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166163 | CACAATGTCTGAATG[A/C]TTAGGCCAGAGACGT | 10055 |
rs144045879 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47171608 | AGGCACCTGCCACCA[C/T]GCTTGGCTAATTTTT | 10055 |
rs144103655 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | SAE1 | GRCh38.p7 | 19:47149381 | TCACCATGTTGGCCA[G/T]GTTGGTCTCAAACTC | 10055 |
rs144107693 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47206087 | GCAGGTAGCCTTGAC[C/G]CCATTGTTGGTGGTA | 10055 |
rs144256195 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47149859 | GAGGCAGGCGGATCA[C/T]GAGGTCAAGAGATTG | 10055 |
rs144258093 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47194935 | TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG | 10055 |
rs144304341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153234 | AGGCATGATCCACTG[C/T]GCCTGGTCTGCTGAC | 10055 |
rs144307837 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129717 | AGATAGCGTTTCCCT[A/G]TATTGACCACCTGGG | 10055 |
rs144338694 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194975 | GTCTCTAACTTCTGA[C/T]CTCGTGATCTGCCTG | 10055 |
rs144380898 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191780 | GTGGGAATAGGCCGG[A/G]CGCGGTGGCTCACAC | 10055 |
rs144414788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134430 | ATGTCATCATGAGGC[A/T]TTAACATTGGTGGGA | 10055 |
rs144472452 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152998 | ATGTTTTTGGCTACC[A/G]TGGATACACATTTGC | 10055 |
rs144474252 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SAE1 | GRCh38.p7 | 19:47179283 | GGCTGAAGCAGGTGG[A/G]TTGCCTGAGCTCAGA | 10055 |
rs144486019 | snp | A/G | 0.000194118 | 0.00984995 | intron-variant | SAE1 | GRCh38.p7 | 19:47180131 | TATCCACTTTTACAC[A/G]TGTTTATTTCCTAGA | 10055 |
rs144525476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141094 | GCAACCTCCGCCTCC[C/T]AGGTTTGAGTGATTC | 10055 |
rs144601429 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47176259 | TCATCTATGACCAGT[C/G]TCATCTTGAAAGGCA | 10055 |
rs144687189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152863 | GATTCACAGTTTGCA[A/G]AACTCAAACCCAGCC | 10055 |
rs144796404 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47158999 | CTGTCATGCTCCCAT[G/T]TTCACGTTTCTTTAT | 10055 |
rs144831071 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SAE1 | GRCh38.p7 | 19:47165194 | TCCTGGGTTCAAGCG[A/G]TTCTCCTGTCTCAGC | 10055 |
rs144858031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47200349 | GCAACACTCTCATCT[C/T]GGCCTCTTGCGTAGC | 10055 |
rs144882876 | snp | C/G | 0.000527426 | 0.0162307 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197362 | GTCCTGACCTGCTTC[C/G]TGAGGACTTTGTCAG | 10055 |
rs144892207 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | SAE1 | GRCh38.p7 | 19:47164253 | GGCTCACTGCAAGCT[C/G]TGCCTCCTGGGTTCA | 10055 |
rs144896742 | snp | C/G | 0.19646 | 0.2442 | intron-variant | SAE1 | GRCh38.p7 | 19:47191977 | GAGAATGGCGTGAAC[C/G]CGGGAGGCGGAGCTT | 10055 |
rs144960507 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47131444 | CGTGCTGCACACAGG[C/G]GAGACTGGACTGGCC | 10055 |
rs144967686 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47206949 | CCATGTGGACAGAGA[A/C]CTCAGAATCCTTAAT | 10055 |
rs145008973 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47160171 | GTAAGTCACTCAGTT[G/T]CCTGGATTGGAACCC | 10055 |
rs145110288 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47209093 | AGACTGCTTTTAGAA[-/T]TTTTTTTTTCCCTCT | 10055 |
rs145122373 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47135833 | GAGTCTCGCCGTGTC[A/G]CCTAGGCTGGAGTAG | 10055 |
rs145137251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47148053 | GCGTGAGCCACCACG[C/T]GTGGCCCTCAACTGT | 10055 |
rs145244833 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SAE1 | GRCh38.p7 | 19:47181146 | ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA | 10055 |
rs145276905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47145450 | CCATCCCCTGCTGAC[A/G]TAATGCTGTTTGATT | 10055 |
rs145405924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47188282 | CTTGAGTTCAGGAGG[G/T]CCAGGCAGCAATGAG | 10055 |
rs145435213 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | SAE1 | GRCh38.p7 | 19:47164941 | ACAGGCGTGAGCCAC[A/C]GTGCCCGGCTAATTT | 10055 |
rs145530875 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47167426 | TTTGTATTTTTAGTA[A/G]AGACGGAGTTTCGCC | 10055 |
rs145607987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161300 | ATAGGCATGAGCCAC[C/T]GTACCCAGCCTATAT | 10055 |
rs145637374 | snp | G/T | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47155203 | CTTCTGAGACAACGA[G/T]GGTCAAAAAGGTATG | 10055 |
rs145662335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171924 | TTTAATGTTATTTAT[A/G]CATTTATTTTTTTGA | 10055 |
rs145737324 | snp | A/G/T | 3.295e-05 | 0.00405881 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169898 | TGCTCTGAAGCGCAC[A/G/T]ACCTCCGACTACTTT | 10055 |
rs145757674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146328 | TTGGGCTTTATGTGT[A/G]GATCAGTAATTACTG | 10055 |
rs145774652 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SAE1 | GRCh38.p7 | 19:47146718 | GTTAGTGGTACGGCC[A/G]GGACCCAGGCATCTG | 10055 |
rs145828090 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SAE1 | GRCh38.p7 | 19:47189311 | GCCTGTAACCCCAGC[A/G]CTTTGGGAGGCTGAG | 10055 |
rs145854716 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SAE1 | GRCh38.p7 | 19:47182125 | TTTCCTCATTCTTCA[A/G]TTTCCCCTCATTCAC | 10055 |
rs145863606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150962 | ACTGCCAAATCTATG[C/T]GGAGGTGAAAGGATA | 10055 |
rs145917612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47188119 | TTTCAGAGGACAAGG[C/T]AGGTGGACAACTTGA | 10055 |
rs145918539 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47143213 | TGGTTTCAAGTGATT[C/T]TCCTGCCTCAGCCTC | 10055 |
rs145945001 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | SAE1 | GRCh38.p7 | 19:47179158 | GATCTCACCACTGCA[C/G]TCCAGCATGGGCGAC | 10055 |
rs146041168 | snp | A/G | 0.000115972 | 0.00761396 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47150366 | GTCATTTTTCACTCA[A/G]TTCGATGCTGTAAGT | 10055 |
rs146064073 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47162513 | CCATTCTGCTGAGTG[G/T]GAAAAATGTGTTTTG | 10055 |
rs146227658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47139511 | TTGTCGGAGAGAAAC[A/G]ATGGTGGCTCAGACT | 10055 |
rs146239736 | in-del | -/TCTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47131728 | TTTTTTTTGAGATAG[-/TCTC]TCTCTGTCGCCCAGG | 10055 |
rs146341629 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SAE1 | GRCh38.p7 | 19:47194452 | AAGTCTACTTTTTCA[A/G]TCAACATATACGGAA | 10055 |
rs146380876 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47138136 | GCAACCTCTGCCTCC[C/T]GGGTTCAGGCAATTC | 10055 |
rs146450271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47171609 | GGCACCTGCCACCAC[A/G]CTTGGCTAATTTTTT | 10055 |
rs146467651 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47169194 | AGACTTACATTCTTG[C/T]CCCTCATTGTGGAAG | 10055 |
rs146510282 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | SAE1 | GRCh38.p7 | 19:47208336 | ACTATTACAGCTCAC[G/T]GCAGCCTCAATGTCC | 10055 |
rs146568647 | in-del | -/CT | 0.0501905 | 0.150254 | intron-variant | SAE1 | GRCh38.p7 | 19:47156469 | GGCGACAGAACGAGA[-/CT]CTGTCTCCAAAAAAA | 10055 |
rs146574019 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47153778 | AATCTAGTTCTTTGG[G/T]CATATTATTATTATT | 10055 |
rs146613550 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47150010 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAATGAGC | 10055 |
rs146641407 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47172961 | GTCAGTGGCTCAAGA[A/T]CACCCATCTAAAACA | 10055 |
rs146683661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47135551 | TCTCTGTCGCGCAGA[C/G]TAGAGTGCAGTGGTG | 10055 |
rs146716185 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SAE1 | GRCh38.p7 | 19:47202766 | AAAATTCAGAGTAGC[C/T]GGGCGTGGTGGCGGG | 10055 |
rs146727723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47207784 | AGACTATAAGCACAC[A/G]CCACCACATCCAACT | 10055 |
rs146733831 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47132510 | CGATCCTCGGCCTCA[A/G]GAGATCTCCCCCCAT | 10055 |
rs146837641 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SAE1 | GRCh38.p7 | 19:47181723 | GCCTCAGGTGATCCT[C/T]CCACCTCAGCCTCCT | 10055 |
rs146849363 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SAE1 | GRCh38.p7 | 19:47187258 | CAGCTATGTCACTCC[C/T]CTGAGCTTCACACCT | 10055 |
rs146944316 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47151882 | GGGGCCATGTTGACC[A/G]CCTTGCAGGCCGTGT | 10055 |
rs146968502 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47156035 | TGAGCCACCATGCCC[A/G]ACCAGAAAACTTTTT | 10055 |
rs146987411 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47192700 | CACCCACCACACTTT[C/T]GGCTAATTTTCCTAT | 10055 |
rs147049824 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47134063 | AGACGGAGTTTCACC[A/G]TGTTGGTCAGGCTGG | 10055 |
rs147052067 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209864 | TGTTCTTGAGTTTTC[A/G]TTTAGGATTAGTTGA | 10055 |
rs147198116 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SAE1 | GRCh38.p7 | 19:47184642 | TCTTGAACTCCTGAC[C/T]TCAGGTGATCCACCC | 10055 |
rs147226727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47179569 | ATTTTGTTTTCAGAT[A/G]AGGTCTTGCTCTGTA | 10055 |
rs147304015 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SAE1 | GRCh38.p7 | 19:47166180 | TAGGCCAGAGACGTG[A/G]GGGTTTGGTGAGAAA | 10055 |
rs147323495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206274 | TGGGAAGCACTTTAC[C/T]TTTTGCCCCATGTCA | 10055 |
rs147333505 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210406 | CTAATGGATAATTCA[A/G]CTAAATAGTGGCTAT | 10055 |
rs147334192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164128 | TTCACTCAATAAGCA[G/T]TCCCCAAATCTGCTT | 10055 |
rs147408194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148893 | TGCTGGGATTACAAG[C/T]GTGAGCCACCGCACC | 10055 |
rs147427971 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47185362 | ACCCAGGTTGGAGTG[C/T]GGTGGTGTGTCGGCT | 10055 |
rs147514338 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130743 | ACATGCAGTCGCCGG[A/C]TCGCCTTTGAGTCTC | 10055 |
rs147515666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47204663 | AGGTTCCCACCACCA[C/T]ACCAGGCTAATTTTT | 10055 |
rs147526201 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47167011 | GGCTGGAGTGTAGTG[A/G]TGTGACCTTGGCTCG | 10055 |
rs147568146 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | SAE1 | GRCh38.p7 | 19:47164342 | CCCGGCTAATTTTTT[C/G]TATTTTTAGTAGAGA | 10055 |
rs147598340 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47160185 | TGCCTGGATTGGAAC[C/T]CTCAGGCCAGAGAGG | 10055 |
rs147639175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175862 | TGCAGATAGTTTTAG[A/G]CACAAAGATTATCTG | 10055 |
rs147701737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142060 | TTGCCTTTTTTCAGC[C/T]TCATCTTCTGTCACT | 10055 |
rs147762158 | snp | A/C/T | 0.000971671 | 0.0220243 | intron-variant, missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47197281 | ATCCCAGTTCTGATA[A/C/T]ATATGAGGAAGATTC | 10055 |
rs147771838 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47155928 | GTATTTTTAGTAGAG[A/G]CGGGGTTCCACCATG | 10055 |
rs147847595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47141200 | AGAGACACGGTTTTG[C/T]CATGTTAGCCAGGCT | 10055 |
rs147910209 | in-del | -/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47171903 | GTTTTTTAAAAAGTA[-/T]TTTTTTTTAATGTTA | 10055 |
rs147934003 | snp | C/T | 9.88777e-05 | 0.00703058 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153037 | GAGAGCATGAGTTTG[C/T]AGAGTAAGTGTTGGG | 10055 |
rs147973329 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47188537 | CCACAGCAAGTGTAT[C/T]GGCTTTTCTAGGGCG | 10055 |
rs148108304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47166107 | TCTCAGGACTTTTTG[C/T]GGGCTGCTTCCCTGT | 10055 |
rs148141853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177437 | AATCATAACTCACTA[C/T]AGCCTTGAACTCCTG | 10055 |
rs148183764 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47151558 | CTCACTGCAACCTCC[A/G]CCTCCCTGGTTTAAG | 10055 |
rs148237581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47157127 | GACTCTCCAGCAAGG[C/T]GGCGTTGGAGATTTT | 10055 |
rs148290933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47162852 | CAAAAATTAGCTGGG[C/T]GTGGTAGCACGTGCC | 10055 |
rs148320884 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | SAE1 | GRCh38.p7 | 19:47204434 | GGATCTCCTGACATC[A/G]TGATCTGCCCACCTC | 10055 |
rs148423503 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SAE1 | GRCh38.p7 | 19:47139707 | CATTCTCCTGTCTCA[C/G]CCTCCCGAGTAGCTG | 10055 |
rs148429414 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47153026 | TGCCAATCTAGGAGA[A/G]CATGAGTTTGTAGAG | 10055 |
rs148433112 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47167532 | GGTGTGAGCCACTGC[A/G]CCCAGCCAACAATTT | 10055 |
rs148473211 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210222 | CCACTTCAGAAGCTT[-/C]CTGAGAGGGAATGGG | 10055 |
rs148519628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47186329 | CTCTATTGGTAAGTA[C/T]AATGCAAATATTTCA | 10055 |
rs148547386 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47159453 | GCTAGACTCCTAGTC[A/C]AGTGTGTAGCACAGT | 10055 |
rs148565971 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47207480 | TCTTCCTCTTTAAAT[-/G]GTAGCTTGTGGTGAA | 10055 |
rs148581540 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SAE1 | GRCh38.p7 | 19:47170485 | CTGATCAACCAACTT[A/C]TCTTCACCGCCCCCC | 10055 |
rs148674714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47144516 | CATCCTGGCTAGCAC[G/T]GTGAAACCCCATCAC | 10055 |
rs148705469 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191284 | GGCGTGGTTGTGGGC[A/G]TCTCCAGCCTGGGTG | 10055 |
rs148728455 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SAE1 | GRCh38.p7 | 19:47149456 | GATTACAGGTGTGAG[C/T]CACCGTGCCCTGCCC | 10055 |
rs148758975 | snp | C/T | 0.021333 | 0.101051 | intron-variant | SAE1 | GRCh38.p7 | 19:47195022 | TGCTGGGATTACAGA[C/T]GTTACAGACGTGAGC | 10055 |
rs148790625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134512 | CTGGACATAGGTGGA[C/G]TGCATTGATTTTAGG | 10055 |
rs148793842 | snp | A/C | 0.00478085 | 0.0486577 | downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47210947 | GTCCCGGAAGCTTCA[A/C]ACTTTTCCACCCTGT | 10055 |
rs148831815 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47188332 | TCCAGCCTGGGTGAC[A/G]GACTGAGGCCATGTC | 10055 |
rs148866219 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47160940 | GCAAGTTTTCCAGGT[A/C]GGAGAGTTAGTTGGG | 10055 |
rs148907690 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47171942 | TTTATTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 10055 |
rs148961061 | snp | C/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169917 | TCCGACTACTTTCTC[C/G]TTCAAGGTGAGGTCT | 10055 |
rs149021112 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SAE1 | GRCh38.p7 | 19:47164377 | TTTCACCGTGTTAGC[C/T]AGGATGGTCTCCATC | 10055 |
rs149040274 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47151189 | AGTTTTGCTCTTGTC[G/T]CCCAGGCTGGAGTGC | 10055 |
rs149083346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47197622 | TTCAAGGCAATGTAA[A/G]ATCTGTAAACATTAT | 10055 |
rs149168322 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47142303 | GCAGGAGAATTGCTT[C/G]GACCTGGGAGGCGGA | 10055 |
rs149198684 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | SAE1 | GRCh38.p7 | 19:47181548 | CAGTGGCATCATCTC[A/G]GCTCACTGCAAGCTC | 10055 |
rs149218920 | in-del | -/TTC | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179911 | TGAAACTACTTACTG[-/TTC]TTCTAAGATTGAGCA | 10055 |
rs149258077 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47152975 | TAGCATCAAGTTCTT[C/T]ACAGGAGATGTTTTT | 10055 |
rs149347504 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47165659 | TTTTTCTTTATAAGC[A/G]TAATGCCAGTGGAGT | 10055 |
rs149359864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47152753 | TTTTGTCTTCTAGCC[A/G]TAGGGCCCAAAGAAC | 10055 |
rs149437427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47137875 | CTCGGATTACAGGCG[C/T]GTGCCACCACACCTG | 10055 |
rs149484644 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47144346 | CTTAAAAAGAAATAA[A/C]TTAATGAAAGGTGTT | 10055 |
rs149518327 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SAE1 | GRCh38.p7 | 19:47156432 | TGCAGTGAGCCGAGA[C/T]GGCAACACTGCACTC | 10055 |
rs149527903 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47191032 | TCTGAAGCTAGATTT[G/T]AGTTTACATTTCTGC | 10055 |
rs149552348 | snp | A/G | | | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129709 | TTTAATAGAGATAGC[A/G]TTTCCCTATATTGAC | 10055 |
rs149561141 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SAE1 | GRCh38.p7 | 19:47204256 | AGGCTGGAGTGCAGT[A/G]GCACGATCTCAGATC | 10055 |
rs149611721 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47134350 | TTTAGAGGGTGCAGT[G/T]GTGGGATGGGAATTA | 10055 |
rs149640513 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SAE1 | GRCh38.p7 | 19:47174466 | CAATGGTGCGATCTC[A/G]GTTCACCACAACCTC | 10055 |
rs149660622 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47167396 | AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 10055 |
rs149766763 | in-del | -/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194633 | GGCTCGAGACTGGCT[-/G]GTGCCCTTTCCTTGG | 10055 |
rs149774540 | snp | A/G | 0.00108667 | 0.0232842 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47169873 | ACTGGAGCAGTGAGA[A/G]AGCAAAGGCTGCTCT | 10055 |
rs149788618 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47158657 | CTGTGGCTGCCCTCA[C/G]TGCCGCAGCCAGCTC | 10055 |
rs149801745 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47145773 | GAGGCCAATCACAGA[A/G]CAGTGCGATTCTGAC | 10055 |
rs149819222 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47200333 | AACCTCCTGGGCTCA[C/G]GCAACACTCTCATCT | 10055 |
rs149873232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206402 | ACTCACCTTTCTCTC[C/T]TGAGGCACTGTCTGA | 10055 |
rs149876961 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47131312 | CAGGAAATCCGAGGC[C/T]CGAAAGCGGTGATTG | 10055 |
rs149930519 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SAE1 | GRCh38.p7 | 19:47135685 | ATTTTAGTACAGGTG[A/G]GGTTTCACCAGGCTA | 10055 |
rs150019691 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | SAE1 | GRCh38.p7 | 19:47181144 | CAACATGGAGAAACC[C/T]CATCTCTACTAAAAA | 10055 |
rs150035434 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | SAE1 | GRCh38.p7 | 19:47163838 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCGTGATCT | 10055 |
rs150106977 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | SAE1 | GRCh38.p7 | 19:47160686 | AGGCGTGAGCCACCG[C/T]GCCCAGCCTAATTTT | 10055 |
rs150137038 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SAE1 | GRCh38.p7 | 19:47202570 | GGATTACAGGCATCA[G/T]CCACTGAGCCCGCCC | 10055 |
rs150187628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133171 | TTTTATTCTAAGTGT[G/T]TGGGAAAACCTGTTG | 10055 |
rs150240456 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | SAE1 | GRCh38.p7 | 19:47136865 | CAGATGAGGAAGGAG[C/G]CTCCACAGAGCAAAT | 10055 |
rs150281615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47150816 | TTTGTCTTAAGAAAA[A/G]CACACCTGATCTTGA | 10055 |
rs150282605 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47178426 | GGGGAAAGTACTGTC[A/T]TAGGAAAGGGAAGCC | 10055 |
rs150311409 | snp | G/T | 0.00970106 | 0.0689677 | intron-variant | SAE1 | GRCh38.p7 | 19:47197400 | TCAGTATTTATCACT[G/T]TTTAGTCTGGACAGA | 10055 |
rs150336219 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47184097 | GAGAGTCAAGCTCTG[G/T]AATCGCCTGACATTT | 10055 |
rs150369408 | snp | A/G | 0.0146672 | 0.084371 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47129442 | TGAGACTACAGGCGT[A/G]TGCCACCACGCCCGG | 10055 |
rs150399316 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47168233 | ACTGTTTTTTTGTAT[A/G]TGTGTTTATATGCGA | 10055 |
rs150459999 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47173885 | AGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 10055 |
rs150548042 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SAE1 | GRCh38.p7 | 19:47148576 | GGGGTGAAATAATTC[C/T]TCTGTTCCAGTCCCC | 10055 |
rs150578315 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SAE1 | GRCh38.p7 | 19:47194351 | ACCAAATACTTGTAT[C/T]TTTTAAAGAGCCTCA | 10055 |
rs150601957 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47152509 | CAATTTAAAAAACTG[A/G]TTTTGCTTGTCCCTG | 10055 |
rs150637960 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SAE1 | GRCh38.p7 | 19:47199865 | CTGTACAGTGTCATC[A/G]GCCGCTGACCTCACG | 10055 |
rs150682076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47131223 | TCTGGGAAGTGGTTG[A/G]GAGGGCCGTTCCGAA | 10055 |
rs150724573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47170982 | GTACCTGGCACTTTT[C/T]TGTTTGTTTTTGAGA | 10055 |
rs150778244 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | SAE1 | GRCh38.p7 | 19:47175688 | GTTGCAGTGAGCCGA[G/T]ATCGTGCCACTGCAC | 10055 |
rs150839840 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47163692 | AGATCGCACCGTTGC[A/G]CTCCAGCCTGGGCGA | 10055 |
rs150956687 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47202495 | GTTTCACCATGTGGG[C/T]CAGGATGATCTCGAT | 10055 |
rs150989428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47140395 | ACAGGTGTGAGCCAC[C/T]GTGCCCAGCCCACGC | 10055 |
rs151008044 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47132738 | CAAAAAAATACAAAA[A/G]TTAGCCAGGCATGGT | 10055 |
rs151037365 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47172171 | TGATCCACCTGCCTC[A/G]GCCTCCCGAAGTGCT | 10055 |
rs151041692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47145494 | TAGAGCCCAACTCCA[A/G]TGTAGCTTTCTCTGA | 10055 |
rs151071909 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SAE1 | GRCh38.p7 | 19:47186684 | CCTCGGAACCTCTTC[A/G]GTAGAGAGTGAGATG | 10055 |
rs151126027 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191783 | GGAATAGGCCGGGCG[C/T]GGTGGCTCACACCTG | 10055 |
rs151168247 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SAE1 | GRCh38.p7 | 19:47164403 | CCATCTGCTGACCTC[A/G]TGATCCGCCCGCCTT | 10055 |
rs151221774 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | SAE1 | GRCh38.p7 | 19:47168123 | GCTTGAACCCAGGAC[A/G]CGGAGGTTGCAGCGA | 10055 |
rs151334386 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47154646 | ATTACAGGCGCCCAC[C/G]ACCACGCCCGGCTAG | 10055 |
rs180767001 | snp | C/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209427 | TCCCATCACCAGCAG[C/T]TGCTCGACAAGGGGC | 10055 |
rs180775969 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47156909 | CGATGGGGAAAGCAA[G/T]ATGAAGGGGCCAGAA | 10055 |
rs180807757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166694 | AATACTGTGTTTCCT[C/T]ATTCTGATGGCATTC | 10055 |
rs180813395 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SAE1 | GRCh38.p7 | 19:47199415 | AAAAAAAAAAAAAAG[A/G]CAGCAATAGAGTGGC | 10055 |
rs180817063 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47139515 | CGGAGAGAAACGATG[C/G]TGGCTCAGACTAGAG | 10055 |
rs180818291 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47187432 | ATGTTTGTAACACTT[C/G]ATAAGAAACAGAACC | 10055 |
rs180830242 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47179523 | AAAAAAAGAAAAACT[C/G]TAAATAAATATTGAA | 10055 |
rs180846314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47146937 | AGTAGAGAAGACTCA[A/G]GTGGATCAGGAAGAA | 10055 |
rs180956905 | snp | A/G | 3.29571e-05 | 0.00405924 | missense, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47143600 | ACCATGCTGGATCAC[A/G]AACAGGTGCGCTGTT | 10055 |
rs181142391 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47188845 | GTACAGAGGACGGGA[C/T]AGGCAAATATTCAGA | 10055 |
rs181156226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47177897 | TAGAGGCTGAGCCTC[A/G]GAGGGGACTGGAGCT | 10055 |
rs181163706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197649 | TTATTCTCTACCTTT[G/T]TTCACTTTATGTGAT | 10055 |
rs181173457 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47147651 | AGAGATGGGGTTTCA[C/T]CATGTTGGCTAGGCT | 10055 |
rs181177348 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209886 | ATTAGTTGAGTTCCA[C/G]CTGGGTTTTGGGAGA | 10055 |
rs181187729 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SAE1 | GRCh38.p7 | 19:47167461 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 10055 |
rs181210089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47162130 | CACAGCTAGTTCTCT[C/T]GGACAGCCCTGCAGG | 10055 |
rs181218876 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47185139 | CATTATATGCTTTTT[A/G]AAAAAACCTAAATGT | 10055 |
rs181279493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143810 | GATGAGCAGTAGAGA[C/T]TCACACCCCCTCATT | 10055 |
rs181299900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133214 | TGTGGGAGTAACATG[A/G]TCTGTTTTTTGTTTG | 10055 |
rs181321848 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47174471 | GTGCGATCTCGGTTC[A/G]CCACAACCTCCACCT | 10055 |
rs181331420 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47205077 | ACTTTGCTATTTGCC[A/C]GAAGATGTTAAATTT | 10055 |
rs181374696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191782 | GGGAATAGGCCGGGC[A/G]CGGTGGCTCACACCT | 10055 |
rs181406917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47151854 | GCCAGTTGATTGTGT[A/G]ATGCGTGTGCATGGG | 10055 |
rs181539225 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47174675 | CCTCCCGGGTTCACG[C/G]CATTCTCCTGCCTCA | 10055 |
rs181545840 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47192353 | CCTCCTGGGTTTGAG[C/T]GACTCCTGCCTCAGG | 10055 |
rs181558579 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134126 | TCGGCCTCCCAAAGT[A/G/T]CTGGGATTACAGGTG | 10055 |
rs181574625 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47152428 | CTTGTTTATCTTCTT[C/T]ATCTTAACATATCAA | 10055 |
rs181685697 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47138295 | GTGATCTACCCGCCT[A/C]AGCCTCCTTAAGTGC | 10055 |
rs181695227 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47155828 | TCACTGCAACCTCCA[C/T]GTCCCAGGTTCAAGA | 10055 |
rs181788983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160887 | GTGGAAATAGGGCAA[C/T]GAGGGGTGTAAATTT | 10055 |
rs181795134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47183961 | TTGGCAAAGCAATGC[A/G]TTAGGGGCCCATGGA | 10055 |
rs181880706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143127 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTTG | 10055 |
rs181970212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47192989 | AGCAGGACATCTACA[A/G]AAGTAGAAGTATTGG | 10055 |
rs181992260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153235 | GGCATGATCCACTGC[A/G]CCTGGTCTGCTGACA | 10055 |
rs182134186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47179060 | AGCCGGGCGTGGTGG[C/T]GGGCGTCTGTAGTCT | 10055 |
rs182190594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47189724 | AACTCCCCTGCCCCC[A/C]ACAATTGAACTGTTT | 10055 |
rs182246023 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47174897 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10055 |
rs182278691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47134469 | GGCACCTGGAATAGA[C/T]TGGGAATTAAGTGAT | 10055 |
rs182283776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47204354 | AGGCGCCTGCCACCA[C/T]GCCCAGCTAATTTTT | 10055 |
rs182363703 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47181162 | TCTCTACTAAAAATA[C/G]AAAATTAGCCAGGCG | 10055 |
rs182382899 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SAE1 | GRCh38.p7 | 19:47200080 | GGATAACAGGCGCCC[A/G]CCACCACGCCCAGCT | 10055 |
rs182399185 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47156389 | GAGGCTGAGGCAGGA[A/G]AATAGCTTGAACTGG | 10055 |
rs182405386 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47140953 | TCTCAGGTTCAAGCG[A/G]TTCTCCTGCCTCAGC | 10055 |
rs182412548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47198015 | TCACTTGGACACTCC[A/C]TGCTTTCACCTTACG | 10055 |
rs182413009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157762 | TGACATTGTTAGTCA[C/G]CTGTTACACTTGAAC | 10055 |
rs182415838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47132406 | GGCGTGCCCCACCAC[A/G]TCATCCGACTAATTT | 10055 |
rs182419109 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179952 | AGTATAGTGTTAATA[A/G]TGAGAATCAAGTTTT | 10055 |
rs182472860 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47171561 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCATCCT | 10055 |
rs182509059 | snp | A/G | 0.000122797 | 0.00783477 | utr-variant-5-prime, nc-transcript-variant, missense, intron-variant | SAE1 | GRCh38.p7 | 19:47130901 | GTTGGCTTGAGCGGG[A/G]CCGGAGCTGAGGCAG | 10055 |
rs182545737 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SAE1 | GRCh38.p7 | 19:47135035 | TTTTAGAAATTAAAA[A/T]TTTTTTTGTGTGAGT | 10055 |
rs182633178 | snp | A/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47202254 | GAACAGAAGAGTAAT[A/T]GTTGATAATATTTGG | 10055 |
rs182694042 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47154083 | CAGGCGTGAGCCACC[A/G]CACCCGGCTATTATT | 10055 |
rs182781318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47148709 | AGCGTCTGCCTCCCA[G/T]GTTCAAGCGATTCTC | 10055 |
rs182799830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47149322 | ATTACAGGCACACAC[C/G]ACCACACCTGGCTTA | 10055 |
rs182810850 | snp | C/G | | | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190773 | GGAAGCTGGTTTACT[C/G]TCTCAAGATTGATGG | 10055 |
rs182814824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47175872 | TTTAGACACAAAGAT[C/T]ATCTGAATTCAGGCC | 10055 |
rs182815491 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SAE1 | GRCh38.p7 | 19:47186025 | TGGGTGGATCACCTG[A/G]GGTCAGGAGTTCAAG | 10055 |
rs182833509 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47207604 | ATGTTGTTTCGGGGG[C/G]TGACCCTGCCTCAAA | 10055 |
rs182841266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47136214 | CACGATCTCAGCCCA[A/G]TACAATCTCCACCTC | 10055 |
rs182949803 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47194623 | CTTAGAGACAAGGCT[C/T]GAGACTGGCTGTGCC | 10055 |
rs183101132 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SAE1 | GRCh38.p7 | 19:47172269 | TGTAGAAATAAATGG[G/T]TTGAGCAGGAATGAG | 10055 |
rs183212280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47175564 | CAAGATGGTGAAATC[A/C]CGTCTCTACTAAAAA | 10055 |
rs183216636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47206889 | GGCAGGTGCTTTTTA[C/T]TTGCCTATTTGCCCA | 10055 |
rs183217642 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47145525 | CCAGGCTCATCTTCA[A/C]GGTGAAAATAAGTGC | 10055 |
rs183233088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47185762 | GTGTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 10055 |
rs183267923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47144775 | AGACTGCTTTGTATA[A/G]TGCTTGAACCTAACA | 10055 |
rs183272286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47164230 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 10055 |
rs183366556 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47205992 | GGGCCGCTGCCCTTG[C/G]ATTGTCAGCCTTACT | 10055 |
rs183368337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47163780 | CGTAGAGTATATGCA[A/G]GTACTGTGCCATTTA | 10055 |
rs183379618 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | SAE1 | GRCh38.p7 | 19:47130566 | TGTCGATTTCACTCA[A/G]TACCGTTATTTTACA | 10055 |
rs183381543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47147906 | TGGGACTACAGGCGC[C/T]CACCACCACGCCTGG | 10055 |
rs183391240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169349 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 10055 |
rs183420455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47164948 | TGAGCCACAGTGCCC[A/G]GCTAATTTTTGTATT | 10055 |
rs183459881 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47194007 | TCTTTTTTTTTTACC[C/T]GGGCATCTGTGGTTT | 10055 |
rs183569088 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47185454 | GGATTACAGGTGCCC[A/G]CCACCATGCCTGGCT | 10055 |
rs183598863 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SAE1 | GRCh38.p7 | 19:47144496 | TGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 10055 |
rs183700892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47142073 | GCCTCATCTTCTGTC[A/G]CTTTACAGATTTAAA | 10055 |
rs183710941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47158232 | GTGCTCCTAAATTAG[C/T]AACGTTGAAAAACAA | 10055 |
rs183981038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182279 | GCCATAGGCAGCCAT[C/T]GCTATTTGGGTATGA | 10055 |
rs183987906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47152054 | GGAACACATTTCTCT[C/G]TGAGTGTTATTTCGG | 10055 |
rs184001281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47202778 | AGCCGGGCGTGGTGG[C/T]GGGTGCCTGTAGTCT | 10055 |
rs184012479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47159004 | ATGCTCCCATGTTCA[C/T]GTTTCTTTATTGTGA | 10055 |
rs184077058 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47141279 | AGTGCTGGGATTACA[A/G]GCGTGAGCCCCCACG | 10055 |
rs184098440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47180392 | CAAGAAGAATAATCA[A/G]TTAATGTAAACAAGG | 10055 |
rs184115446 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SAE1 | GRCh38.p7 | 19:47209505 | CCGGGCCTGCCAGCT[C/T]CCCTGAGTGATGAGC | 10055 |
rs184237535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157934 | TTTGGCCATGGCTTT[A/G]TCACCTTGCAATAAC | 10055 |
rs184241244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47201693 | GGCTGGAGTGCAGTG[A/G]CACCATCTCGGCTCA | 10055 |
rs184287593 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SAE1 | GRCh38.p7 | 19:47177369 | TTTGTTTGTTTTTTT[C/T]CCCCCCCAAAACAGG | 10055 |
rs184316984 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47138142 | TCTGCCTCCCGGGTT[C/T]AGGCAATTCTCCTGC | 10055 |
rs184320798 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47155639 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 10055 |
rs184427970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133095 | AAATTCCCAGAGGCC[C/G]AGGCATGATTGTCAA | 10055 |
rs184443341 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47173478 | TCCCCTCAGTTCAAT[G/T]ACCCCTGTGATGTTG | 10055 |
rs184520278 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47146103 | AGCAGTGTCACAAAG[C/G]CACCCTACAGTGTGG | 10055 |
rs184524827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47166570 | CCTCCACCCCCAACT[C/G]CGTTTCATCATATAG | 10055 |
rs184528378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47191537 | GGCTGCTTATAGGGC[A/G]CAGTCTGAGGCCTTG | 10055 |
rs184537375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47187281 | TCACACCTATGGACT[A/G]TTCTGCACCCTAGCC | 10055 |
rs184562450 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SAE1 | GRCh38.p7 | 19:47151412 | TGCCTCGGCCTCCCA[A/G]AGTGGTGGGATTACA | 10055 |
rs184587071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47178155 | GGGAGGCAGGAGAAT[C/T]GCTTGAAAACCTGGA | 10055 |
rs184596033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197682 | TGTTATCTCTTGGGG[A/G]CATCTCCAGATCAGT | 10055 |
rs184627164 | snp | G/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47155979 | CTCTTGACCTCGTGG[G/T]CCACCTGCCTCAGCC | 10055 |
rs184678626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47208603 | GCTAATTTCTGTATT[G/T]TTAGTAGAGACAGGT | 10055 |
rs184719232 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47142595 | CTCGAAGAAAATCCA[C/G]AATCCTTCCATTGCA | 10055 |
rs184743592 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47192011 | GTGAGCCGAGATCGC[A/G]CCACCGCACTCCAGC | 10055 |
rs184847764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47173007 | CTGGAAGCCAGGTCT[A/G]TTTTGATTCCAAAGG | 10055 |
rs184853787 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | SAE1 | GRCh38.p7 | 19:47190948 | CAGACCACTTGGAAT[A/C]CTAGGTGCTGTGTCC | 10055 |
rs184878398 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47132654 | TGGGAAGCTGAGTTG[A/C/G]GGGGAGGGGACCTCT | 10055 |
rs185019310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47197093 | GGCTGAGGCAGAAGA[A/T]TCACTTGAACCCGGG | 10055 |
rs185100834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47204764 | GCCTCCCAAAGTGCT[C/G]GGATTATAGGTGTGA | 10055 |
rs185131073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47143751 | CTCTGGAGACTGAAG[C/G]TGCTATTGTTGGGTT | 10055 |
rs185134727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47161659 | TGATTTCGCTCACCA[C/T]CATAGACCTACCACT | 10055 |
rs185143810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47184102 | TCAAGCTCTGGAATC[A/G]CCTGACATTTTTAAG | 10055 |
rs185204473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47145972 | CGGAAACCATAGCAG[A/G]CTCCCTGACTGAGGT | 10055 |
rs185221708 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SAE1 | GRCh38.p7 | 19:47208003 | ATTGCCATTGCTAAA[G/T]AGCATTGTCCAGGCC | 10055 |
rs185252303 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47165408 | TTATTAGTCTTAACT[A/G]GATTGTTGATTGAAG | 10055 |
rs185260425 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47138557 | ATGGACACAGGTTTG[C/G/T]TTTGGTGTGTCTATT | 10055 |
rs185371152 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SAE1 | GRCh38.p7 | 19:47196449 | GTTCACTGCAACTTC[C/T]GCCTGCTGGATTCAA | 10055 |
rs185374071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47186642 | AAGTGCATGCTCCTT[A/T]TCCCCATCAACAACT | 10055 |
rs185465355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47205192 | AATGATTGGCCATGT[C/G]CATGTACATGTCAAG | 10055 |
rs185508040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47133415 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10055 |
rs185515530 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SAE1 | GRCh38.p7 | 19:47137140 | CAGCCTGTAATCCCA[A/G]GACTTTGAGAGGCCG | 10055 |
rs185533352 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | SAE1 | GRCh38.p7 | 19:47176768 | AGTGGCCAGACTGTA[C/T]GCTTCCTGCTGCATT | 10055 |
rs185579553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47157299 | TTTCTTTCTTTTTGA[G/T]GCCCAGTCAAGATTT | 10055 |
rs185586051 | snp | A/G | | | intron-variant | SAE1 | GRCh38.p7 | 19:47179649 | CTCCCAGCTCAAGCA[A/G]TCCTCACATCACAGC | 10055 |
rs185596193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47199467 | GAGACATGGAAAAGC[A/G]GTTTCCCCAAAGAGG | 10055 |
rs185613942 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SAE1 | GRCh38.p7 | 19:47140115 | GCTAATTTTTTTTTT[C/T]TTTCTTTTTGAAACA | 10055 |
rs185691055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47182806 | ACTGGTTACAGGCGG[A/G]GTGTGGTGGCTCAGG | 10055 |
rs185728547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SAE1 | GRCh38.p7 | 19:47143347 | TGACCTCAAGTGATC[C/T]GCCTATCTCAGCCTC | 10055 |
rs185788740 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SAE1 | GRCh38.p7 | 19:47204340 | GTAGCTGGGACTACA[A/G]GCGCCTGCCACCACG | 10055 |
rs185816317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47160543 | GGGACTACAGATGCC[C/T]GCCGCCATGCCCGAC | 10055 |
rs185911281 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SAE1 | GRCh38.p7 | 19:47200858 | TTATCTGGTTCTTTT[G/T]TTTGTTTGTTTGTTT | 10055 |
rs185987381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SAE1 | GRCh38.p7 | 19:47175356 | ATGGTTGTGATTGCC[A/G]AAAGTCATATCCGTG | 10055 |
rs186019232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SAE1 | GRCh38.p7 | 19:47134503 | AATGTGCCTCTGGAC[A/G]TAGGTGGACTGCATT | 10055 |
rs186156032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47153321 | GGCATATTCAACCAA[A/G]GTCTACCTTGGAAAA | 10055 |
rs186159383 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SAE1 | GRCh38.p7 | 19:47147742 | ACAGGTGTGAGCCAC[C/T]GTGCCCAGCCTCAAC | 10055 |
rs186338794 | snp | C/T | | | intron-variant | SAE1 | GRCh38.p7 | 19:47163122 | GTATTTTTCTATGTA[C/T]ATACAACAAAATTGG | 10055 |
rs186400978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SAE1 | GRCh38.p7 | 19:47169743 | TGAGATTTTTCTGCA[A/G]TAGAGAAGAGCAACT | 10055 |