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 |