SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8482 | snp | A/G | 0.491535 | 0.0645033 | downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB, missense | NBR1, TMEM106A | GRCh38.p7 | 17:43209941 | CAGCCCTGATGGCCC[A/G]TCTCTTTGAAATGGG | 4077 |
rs13119 | snp | A/G | 0.446249 | 0.154875 | utr-variant-3-prime, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43210702 | CTTTCATTGAAATGC[A/G]GAGATTCCCTTGAAG | 4077 |
rs748620 | snp | C/G | 0.456685 | 0.140646 | downstream-variant-500B, utr-variant-3-prime, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43210253 | AACTAAAGACCAGAA[C/G]TTAAATTTTCACTTT | 4077 |
rs1054404 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43210845 | CTAATCTTATAGAAA[A/G]GGAAAAAATCCCGTT | 4077 |
rs1065402 | snp | C/T | 0 | 0 | utr-variant-3-prime, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43211394 | AATGGTGATTTTAAT[C/T]AGTCATTAGCCATAA | 4077 |
rs1399323 | snp | A/G | 0.45692 | 0.1403 | intron-variant | NBR1 | GRCh38.p7 | 17:43180313 | AGGTTCGCAGCCTAT[A/G]AGCAATAGGTTATAC | 4077 |
rs1565163 | snp | C/T | 0.453209 | 0.145623 | intron-variant | NBR1 | GRCh38.p7 | 17:43209323 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCATGAGG | 4077 |
rs2011316 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | NBR1, LOC101929767, LOC107985003 | GRCh38.p7 | 17:43168546 | gttcaagcgattctc[A/C]tgcctcagctcccga | 4077 |
rs2271572 | snp | C/T | 0.0100192 | 0.0700658 | intron-variant | NBR1 | GRCh38.p7 | 17:43189136 | CAGTTAAAACCCAAG[C/T]GAGACAGAACACTCA | 4077 |
rs2271573 | snp | A/G | 0.445328 | 0.156035 | intron-variant | NBR1 | GRCh38.p7 | 17:43175604 | TTCTTTCCTGAAACA[A/G]TTCCTATTTAACAGT | 4077 |
rs2271574 | snp | C/T | 0.456685 | 0.140646 | intron-variant | NBR1 | GRCh38.p7 | 17:43175631 | CAGTGATGGTAAGTT[C/T]CGTAAGAACAGGGAC | 4077 |
rs2306829 | snp | A/G | 0.46024 | 0.135275 | intron-variant | NBR1 | GRCh38.p7 | 17:43201789 | GAAAAAGCTTAGGCT[A/G]ATCATTACCTCCTCT | 4077 |
rs2356310 | snp | C/T | 0.499989 | 0.00239614 | intron-variant | NBR1 | GRCh38.p7 | 17:43207570 | TTTCACTGTGTTGCC[C/T]AGGGCAACTAACTCC | 4077 |
rs3206411 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43211266 | AGAGGTAACAAAAAA[C/T]GCTAAATATTTTATC | 4077 |
rs3215228 | in-del | -/T | 0.446249 | 0.154875 | intron-variant | NBR1 | GRCh38.p7 | 17:43175633 | TGATGGTAAGTTTCG[-/T]TAAGAACAGGGACAG | 4077 |
rs3744242 | snp | C/T | 0.44651 | 0.154543 | intron-variant | NBR1 | GRCh38.p7 | 17:43194781 | GCTGCATTTTCTCTT[C/T]CCTGCTATTGGGTTA | 4077 |
rs3744243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NBR1 | GRCh38.p7 | 17:43203562 | GCAATTGTGTTCTCT[C/T]TTTCCATCTAATTTT | 4077 |
rs4239149 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | NBR1 | GRCh38.p7 | 17:43176078 | ATGAGATGTGCCCCA[A/G]TAAAGGGAACCAACA | 4077 |
rs4239150 | snp | A/G | 0.205723 | 0.246048 | intron-variant | NBR1 | GRCh38.p7 | 17:43176206 | AGTGAATTGGTGTGG[A/G]CTCCACCCAACCAGA | 4077 |
rs4445938 | snp | A/C | 0.45692 | 0.1403 | intron-variant | NBR1 | GRCh38.p7 | 17:43185883 | GCACCTGTATGTAAT[A/C]CCAGCTACTTGGGAG | 4077 |
rs4793216 | snp | A/G | 0.451234 | 0.14834 | intron-variant | NBR1 | GRCh38.p7 | 17:43183455 | caatctcttgacctc[A/G]tgatccacctgcctt | 4077 |
rs4793217 | snp | A/G | 0.44638 | 0.154709 | intron-variant | NBR1 | GRCh38.p7 | 17:43194266 | TGGAGGTACAGCAGC[A/G]TTTTTATTTTTGGGG | 4077 |
rs5820485 | in-del | -/A | 0.192401 | 0.243274 | utr-variant-3-prime, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43210945 | CAGTGGGGGAAATAG[-/A]AAACATGTGAAAGGC | 4077 |
rs7220009 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | NBR1 | GRCh38.p7 | 17:43178695 | ATAACTTTTAAAATT[A/G]TATAGTGACCTTAAG | 4077 |
rs8069921 | snp | A/G | 0 | 0 | intron-variant | NBR1 | GRCh38.p7 | 17:43189914 | GTTTCTGAGCATTAG[A/G]TGTTGTAGCTGTGAG | 4077 |
rs8070085 | snp | A/G | 0.458084 | 0.138567 | intron-variant | NBR1 | GRCh38.p7 | 17:43189967 | ACCCACATGCTTTGT[A/G]TGTTGTAACTATTCA | 4077 |
rs8070089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NBR1 | GRCh38.p7 | 17:43189978 | TTGTATGTTGTAACT[A/G]TTCAGATTGTTGTGT | 4077 |
rs8070233 | snp | A/G | 0 | 0 | intron-variant | NBR1 | GRCh38.p7 | 17:43190061 | GGACAAAATTAGATC[A/G]CTAAGGGTAGTTCCT | 4077 |
rs8074136 | snp | A/C | 0.457154 | 0.139954 | intron-variant | NBR1 | GRCh38.p7 | 17:43190296 | GGCTAGTCTCAAACT[A/C]CTGGACTCAAATGAT | 4077 |
rs8076993 | snp | C/G | | | intron-variant | NBR1 | GRCh38.p7 | 17:43182396 | ctaatttattttgta[C/G]tttttagtagagaca | 4077 |
rs9747601 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | NBR1 | GRCh38.p7 | 17:43204380 | GCATGAATAAAACAC[C/T]AGTTCTTggccgggt | 4077 |
rs9904555 | snp | C/T | 0.0191063 | 0.0958546 | intron-variant | NBR1 | GRCh38.p7 | 17:43180787 | GTGTATATTTTTTGT[C/T]CTTTTAGGAGAATAT | 4077 |
rs9908561 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | NBR1 | GRCh38.p7 | 17:43191087 | caagatcccgcctct[A/G]caaaaaaaatttaaa | 4077 |
rs9908805 | snp | C/T | 0.206642 | 0.246211 | upstream-variant-2KB, intron-variant | NBR1, LOC101929767, LOC107985003 | GRCh38.p7 | 17:43169893 | TTCCCCCCCTCTACA[C/T]TGCAGATGTGGCTCC | 4077 |
rs9910360 | snp | A/C | 0 | 0 | upstream-variant-2KB, nc-transcript-variant, intron-variant | NBR1, LOC101929767, LOC107985003 | GRCh38.p7 | 17:43170239 | TTATCTGTAATTCCC[A/C]CGCTTTACTGTTGCC | 4077 |
rs10684756 | in-del | -/TG | 0.0185938 | 0.0946107 | intron-variant | NBR1 | GRCh38.p7 | 17:43175667 | TCTTTTGTTCATTGC[-/TG]TGTCTCCCAAGCCCA | 4077 |
rs11322550 | in-del | -/T | 0.495095 | 0.0492773 | downstream-variant-500B, intron-variant, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43209863 | TTAAATTATACAGAA[-/T]TTTTTTTTTTTTTTT | 4077 |
rs11409840 | in-del | -/A | 0.5 | 0 | intron-variant | NBR1 | GRCh38.p7 | 17:43202525 | AAAAAAAAAAAAAAA[-/A]GACTTCAAACACTGT | 4077 |
rs11538738 | snp | C/G | 1.6908e-05 | 0.00290753 | missense | NBR1 | GRCh38.p7 | 17:43201699 | AGGAGCTCTCCTTGT[C/G]TACATCATCATGGTT | 4077 |
rs11650132 | snp | G/T | 0.44638 | 0.154709 | intron-variant | NBR1 | GRCh38.p7 | 17:43174070 | CATGATAATGATATC[G/T]AGACTGTTTTTAAAA | 4077 |
rs11650272 | snp | A/G | 0.463774 | 0.129618 | intron-variant | NBR1 | GRCh38.p7 | 17:43174491 | tagtcccagctactc[A/G]ggaggctgaggtgag | 4077 |
rs11650913 | snp | C/T | 0.447162 | 0.153712 | intron-variant | NBR1 | GRCh38.p7 | 17:43179580 | GCAGTTTTTTATATA[C/T]AGGATGATGCCTTTG | 4077 |
rs11651623 | snp | A/G | 0.44638 | 0.154709 | intron-variant | NBR1 | GRCh38.p7 | 17:43177830 | TTAACCCTTTGTTAT[A/G]GGTTATTAAGGTTGT | 4077 |
rs11651757 | snp | C/G | | | intron-variant | NBR1 | GRCh38.p7 | 17:43185419 | aaaatacaaaagtta[C/G]ccaggtatggtggtg | 4077 |
rs11653231 | snp | A/G | 0.457361 | 0.139647 | intron-variant | NBR1 | GRCh38.p7 | 17:43179443 | AGTCTGTTCAGCCTT[A/G]TTTAAAAACCTTAAT | 4077 |
rs11653460 | snp | C/T | 0.447291 | 0.153545 | intron-variant | NBR1 | GRCh38.p7 | 17:43179289 | TATGGAAAAGCTGAA[C/T]GCTTGGCCTGAGTTT | 4077 |
rs11654700 | snp | A/G | 0.446249 | 0.154875 | intron-variant | NBR1 | GRCh38.p7 | 17:43174881 | caggcagatcatgag[A/G]tcaggagatcgagac | 4077 |
rs11654731 | snp | A/G | 0.446249 | 0.154875 | intron-variant | NBR1 | GRCh38.p7 | 17:43174923 | ACACGGTGAAACCCC[A/G]TCCCTACCAAAAATA | 4077 |
rs11654877 | snp | A/G | 0.45692 | 0.1403 | intron-variant | NBR1 | GRCh38.p7 | 17:43188672 | CAGTTTCAGTTTTCT[A/G]CATATGGCTAGCCAG | 4077 |
rs11655049 | snp | C/T | 0.451109 | 0.148509 | intron-variant | NBR1 | GRCh38.p7 | 17:43182908 | agctgggattacagg[C/T]gtatgccaccatgcc | 4077 |
rs11656843 | snp | A/G | 0.461259 | 0.133677 | intron-variant | NBR1 | GRCh38.p7 | 17:43187470 | caggcgtgagccacc[A/G]cgcccggcctccaac | 4077 |
rs11656945 | snp | A/G | 0.446249 | 0.154875 | intron-variant | NBR1 | GRCh38.p7 | 17:43178248 | AAACAGGGTCTCACT[A/G]TGTTGCTCAGGCCAG | 4077 |
rs11657883 | snp | C/T | 0.476022 | 0.106836 | intron-variant | NBR1 | GRCh38.p7 | 17:43178007 | TGAAGAGGTAAAATA[C/T]ATTATGGCACTTATT | 4077 |
rs11658499 | snp | C/T | 0.447032 | 0.153878 | intron-variant | NBR1 | GRCh38.p7 | 17:43182732 | gttaattaacacatc[C/T]atcacctcagatgta | 4077 |
rs12103881 | snp | G/T | 0 | 0 | intron-variant | NBR1 | GRCh38.p7 | 17:43178394 | ctttttttttttttg[G/T]gagatgaagcctcac | 4077 |
rs12936831 | snp | C/T | 0.447162 | 0.153712 | intron-variant | NBR1 | GRCh38.p7 | 17:43179799 | TCAGAGCTTGGAGTG[C/T]ATTTTCCCATAGGAA | 4077 |
rs12937192 | snp | A/G | 0.45645 | 0.140991 | intron-variant | NBR1 | GRCh38.p7 | 17:43173473 | TTGTATTTTTAGTAG[A/G]GACGAGGTTTCACCA | 4077 |
rs12940037 | snp | A/G | 0.446249 | 0.154875 | intron-variant | NBR1 | GRCh38.p7 | 17:43173325 | acagagtctcgctct[A/G]tcacccaggcgagag | 4077 |
rs12944430 | snp | C/G | 0.44651 | 0.154543 | intron-variant | NBR1 | GRCh38.p7 | 17:43178803 | aaagagggtctcact[C/G]tgttgcccaggctgg | 4077 |
rs12948939 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NBR1 | GRCh38.p7 | 17:43184691 | ATTTTTATTGGAAAA[A/G]TAAATGCTTAATTAT | 4077 |
rs12952012 | snp | C/T | 0.452842 | 0.146134 | upstream-variant-2KB, intron-variant | NBR1, LOC101929767, LOC107985003 | GRCh38.p7 | 17:43169370 | GACGGGGTTTCACCA[C/T]GATGGTCAGGCTGGT | 4077 |
rs17139254 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | NBR1 | GRCh38.p7 | 17:43199973 | TTTCTGTGAGCTTTG[A/G]TTCTATTTTGTTTTG | 4077 |
rs17527802 | snp | A/G | 0.458545 | 0.137872 | intron-variant | NBR1 | GRCh38.p7 | 17:43197696 | AGTTGTGCTGCCTGG[A/G]TTCTGCAGTAAGGAA | 4077 |
rs17527829 | snp | A/G | 0.44638 | 0.154709 | intron-variant | NBR1 | GRCh38.p7 | 17:43199714 | TTTACCCTCTCAAAC[A/G]TGATTGGCCAGTTTT | 4077 |
rs17527933 | snp | A/G | 0.480461 | 0.0968913 | intron-variant | NBR1 | GRCh38.p7 | 17:43202871 | TAAAGGCTTTGAGCA[A/G]CACTGAACAAACGGC | 4077 |
rs17599948 | snp | A/G | 0.291235 | 0.246576 | intron-variant | NBR1 | GRCh38.p7 | 17:43201393 | GCTGGAGCCTTGACT[A/G]TAATGTAAACCATTC | 4077 |
rs28728414 | snp | C/T | | | intron-variant | NBR1 | GRCh38.p7 | 17:43180883 | GGTTGGTTTTTTTTC[C/T]TTTTTTGAGATGAGG | 4077 |
rs33911743 | snp | A/T | 0.458545 | 0.137872 | intron-variant | NBR1 | GRCh38.p7 | 17:43192295 | CCAAAATGGTGAGAT[A/T]ACAGGTGTGAGCCAC | 4077 |
rs33918839 | snp | C/T | 0.456685 | 0.140646 | intron-variant | NBR1 | GRCh38.p7 | 17:43177155 | GCAGGCACCTGTGGT[C/T]CCAGCTACTCCGGAG | 4077 |
rs33920795 | snp | A/G | 0.456685 | 0.140646 | intron-variant | NBR1 | GRCh38.p7 | 17:43176993 | AAACATTATTTGGCC[A/G]GGCACAGTGGCACAC | 4077 |
rs33924658 | snp | C/T | 0.44638 | 0.154709 | intron-variant | NBR1 | GRCh38.p7 | 17:43192485 | GCCATTCTCCTGCCT[C/T]AGCCTCCCGAGTAAC | 4077 |
rs33936469 | in-del | -/A | | | utr-variant-3-prime, upstream-variant-2KB | NBR1, TMEM106A | GRCh38.p7 | 17:43210948 | TGGGGGAAATAGAAA[-/A]CATGTGAAAGGCAAA | 4077 |
rs33946455 | snp | C/T | 0.456685 | 0.140646 | upstream-variant-2KB, intron-variant | NBR1, LOC101929767, LOC107985003 | GRCh38.p7 | 17:43169829 | AACCCCACGGCCTGT[C/T]CCCCGTCCAGAACGT | 4077 |
rs33994002 | snp | A/T | 0.456803 | 0.140473 | intron-variant | NBR1 | GRCh38.p7 | 17:43176801 | GTAAATTTTAAATTG[A/T]ATAAGTATAATACAT | 4077 |
rs34142696 | snp | A/C | 0.458545 | 0.137872 | intron-variant | NBR1 | GRCh38.p7 | 17:43196131 | ATCTCAAAAAAAAAA[A/C]AAAAAGCAATAAAAC | 4077 |
rs34234065 | snp | C/T | 0.458545 | 0.137872 | intron-variant | NBR1 | GRCh38.p7 | 17:43195799 | GCTCTCCAGCCTGGA[C/T]GACAGAGTGAAACCC | 4077 |
rs34257545 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NBR1 | GRCh38.p7 | 17:43206335 | TTTTAGTAAGATTAC[C/T]GGCTACATTGTAGAG | 4077 |
rs34365396 | snp | A/G | 0.44651 | 0.154543 | intron-variant, upstream-variant-2KB | NBR1, LOC107985003 | GRCh38.p7 | 17:43173003 | CCGTCTCTACTAAAA[A/G]TACAAAAAATTTAGC | 4077 |
rs34372250 | snp | A/G | 0.00518303 | 0.0506424 | missense | NBR1 | GRCh38.p7 | 17:43196947 | TGTCTTTCAGATTCT[A/G]TGGTGTCAGTAAAGA | 4077 |
rs34415980 | in-del | -/A | 0.5 | 0 | intron-variant | NBR1 | GRCh38.p7 | 17:43197519 | TCAAAAAAAAAAAAA[-/A]GAAATTCTGATCTTG | 4077 |
rs34603377 | snp | A/G | 0.132066 | 0.220435 | intron-variant | NBR1 | GRCh38.p7 | 17:43201451 | TTGACACCACTTGAT[A/G]TAGGTGGGGACATGA | 4077 |
rs34660735 | in-del | -/C | | | frameshift-variant | NBR1 | GRCh38.p7 | 17:43200372 | CTTTGATACCAGCCG[-/C]CCCCTGGGGGATTCT | 4077 |
rs34662447 | in-del | -/G | | | intron-variant | NBR1 | GRCh38.p7 | 17:43198201 | AATACCTTTATAACA[-/G]GAAACTTCTAGGTAT | 4077 |
rs34682023 | in-del | -/T | | | intron-variant | NBR1 | GRCh38.p7 | 17:43190093 | GTTGTTCCAAATGCC[-/T]TTTTTTTTTTTTTTT | 4077 |
rs34725381 | in-del | -/TT | 0.0189856 | 0.0955633 | intron-variant | NBR1 | GRCh38.p7 | 17:43183447 | GGTGGTCTCAATCTC[-/TT]GACCTCGTGATCCAC | 4077 |
rs34734420 | in-del | -/A | | | intron-variant | NBR1 | GRCh38.p7 | 17:43206655 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAGGA | 4077 |
rs34743495 | snp | A/G | 0.445987 | 0.155207 | intron-variant | NBR1 | GRCh38.p7 | 17:43197295 | GAGGCCAAGGCAGGC[A/G]GATCACAAGGTCAGG | 4077 |
rs34757581 | in-del | -/C | | | intron-variant | NBR1 | GRCh38.p7 | 17:43175064 | GATCGTGCCACTGCA[-/C]CCCCAGCCTGGGGCG | 4077 |
rs34765759 | in-del | -/C | | | intron-variant, upstream-variant-2KB | NBR1, LOC107985003 | GRCh38.p7 | 17:43172432 | GAGAGGAAGATTCAT[-/C]TTCCTTCACAAGTAG | 4077 |
rs34787155 | in-del | -/AA | | | intron-variant | NBR1 | GRCh38.p7 | 17:43195652 | GCAAAACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 4077 |
rs34915678 | in-del | -/T | 0.493201 | 0.0579089 | intron-variant | NBR1 | GRCh38.p7 | 17:43199088 | AGGATTTATGGGTAA[-/T]TTTTTTTTTTTTTTT | 4077 |
rs34920601 | in-del | -/T | 0.452965 | 0.145963 | intron-variant | NBR1 | GRCh38.p7 | 17:43192020 | CACACAGCACCCGGC[-/T]TTTTTTTTTTTTTTT | 4077 |
rs34966890 | in-del | -/G | | | intron-variant | NBR1 | GRCh38.p7 | 17:43198280 | AAATATACTATGTCA[-/G]AAATAATATTGGAGA | 4077 |
rs34982101 | snp | A/T | 0.461703 | 0.132974 | intron-variant | NBR1 | GRCh38.p7 | 17:43197319 | GGTCAGGAGATCAAG[A/T]CCATCCTGGCTAACA | 4077 |
rs34999923 | snp | A/T | 0.491757 | 0.0636676 | intron-variant | NBR1 | GRCh38.p7 | 17:43202523 | ACTTCCCAAATACTT[A/T]AAAAAAAAAAAAAAA | 4077 |
rs35014595 | snp | A/G | 0.495135 | 0.0490805 | intron-variant | NBR1 | GRCh38.p7 | 17:43187680 | ACTGCTAAAAATACA[A/G]AAAATTAGCCAGGTG | 4077 |
rs35017602 | snp | A/G | 0.480461 | 0.0968913 | intron-variant | NBR1 | GRCh38.p7 | 17:43201994 | ACCAGCCTGGCCAAC[A/G]TAGTGAAACCCTGTC | 4077 |
rs35043576 | snp | C/T | 0.00299811 | 0.0386014 | synonymous-codon, intron-variant | NBR1 | GRCh38.p7 | 17:43191498 | CCATAGGAAAATTCA[C/T]CTGTGGAATTCAATC | 4077 |
rs35044057 | in-del | -/A | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | NBR1, LOC101929767, LOC107985003 | GRCh38.p7 | 17:43172037 | CAGGTCTGTTTCATT[-/A]AAGGGATTTTGTTGA | 4077 |
rs35122224 | in-del | -/G | | | intron-variant | NBR1 | GRCh38.p7 | 17:43176227 | CCAACCAGATCCCAA[-/G]GGAAATGTTCTCTTG | 4077 |