Item | Value |
---|---|
geneid | 55137 |
ensemblid | ENSG00000182263.14 |
hgncid | 13285 |
symbol | FIGN |
name | fidgetin, microtubule severing factor |
refseq_nuc | NM_018086.4 |
refseq_prot | NP_060556.2 |
ensembl_nuc | ENST00000333129.4 |
ensembl_prot | ENSP00000333836.3 |
mane_status | MANE Select |
chr | chr2 |
start | 163602611 |
end | 163736008 |
strand | - |
ver | v1.2 |
region | chr2:163602611-163736008 |
region5000 | chr2:163597611-163741008 |
regionname0 | FIGN_chr2_163602611_163736008 |
regionname5000 | FIGN_chr2_163597611_163741008 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 759 | 263 | 80 | 33 | 114 | 8 | 26 | 85 | FIGN_chr2_163597611_163741008 | FIGN | MISST others(754): Show |
chr2 | 163597611 | 163741008 |
a0002 | 0/0 | 759 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | MISST others(754): Show |
chr2 | 163597611 | 163741008 |
a0003 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | MISST others(754): Show |
chr2 | 163597611 | 163741008 |
a0004 | 0/0 | 759 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | MISST others(754): Show |
chr2 | 163597611 | 163741008 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2277 | 238 | 66 | 30 | 106 | 8 | 26 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0001c0002 | 0/0 | 2277 | 15 | 14 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0001c0003 | 0/0 | 2277 | 6 | 0 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0001c0004 | 0/0 | 2277 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0001c0008 | 0/0 | 2277 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0001c0009 | 0/0 | 2277 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0002c0005 | 0/0 | 2277 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0003c0006 | 0/0 | 2277 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 | ||
a0004c0007 | 0/0 | 2277 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | ATGAT others(2272): Show |
chr2 | 163597611 | 163741008 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 9543 | 54 | 9 | 12 | 18 | 5 | 9 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0002 | 0/0 | 9545 | 27 | 0 | 0 | 25 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0003 | 1/0 | 9537 | 13 | 12 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9532): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0004 | 0/0 | 9544 | 9 | 3 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0005 | 0/0 | 9543 | 9 | 4 | 0 | 3 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0006 | 0/0 | 9544 | 10 | 3 | 5 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0007 | 0/0 | 9534 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9529): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0008 | 0/0 | 9538 | 6 | 0 | 0 | 6 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9533): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0009 | 0/0 | 9542 | 3 | 1 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9537): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0010 | 0/0 | 9546 | 5 | 0 | 0 | 5 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0011 | 0/0 | 9544 | 3 | 2 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0012 | 0/0 | 9544 | 4 | 0 | 0 | 0 | 0 | 4 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0013 | 0/0 | 9546 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0014 | 0/0 | 9545 | 3 | 0 | 0 | 1 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0015 | 0/0 | 9541 | 3 | 3 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9536): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0016 | 0/0 | 9543 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0017 | 0/0 | 9543 | 3 | 0 | 0 | 3 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0018 | 0/0 | 9544 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0019 | 0/0 | 9543 | 3 | 0 | 3 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0020 | 0/0 | 9543 | 3 | 0 | 0 | 1 | 0 | 2 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0021 | 0/0 | 9546 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0022 | 0/0 | 9544 | 2 | 0 | 1 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0023 | 0/0 | 9543 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0024 | 0/0 | 9541 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9536): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0025 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0026 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0027 | 0/0 | 9544 | 2 | 1 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0029 | 0/0 | 9545 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0030 | 0/0 | 9542 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9537): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0031 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0032 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0034 | 0/0 | 9542 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9537): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0035 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0036 | 0/0 | 9545 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0037 | 0/0 | 9544 | 2 | 0 | 1 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0038 | 0/0 | 9545 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0039 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0040 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0041 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0042 | 0/0 | 9543 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0043 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0044 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0045 | 0/0 | 9545 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0046 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0047 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0048 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0049 | 0/0 | 9545 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0050 | 0/0 | 9546 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0051 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0052 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0053 | 0/0 | 9543 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0055 | 0/0 | 9541 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9536): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0056 | 0/0 | 9539 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9534): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0057 | 0/0 | 9534 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9529): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0058 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0059 | 0/0 | 9550 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9545): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0060 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0061 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0062 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0063 | 0/0 | 9548 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9543): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0064 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0065 | 0/0 | 9543 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0066 | 0/0 | 9538 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9533): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0067 | 0/0 | 9537 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9532): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0069 | 0/0 | 9543 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0070 | 0/0 | 9545 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0071 | 0/0 | 9542 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9537): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0072 | 0/0 | 9541 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9536): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0073 | 0/0 | 9536 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9531): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0074 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0075 | 0/0 | 9543 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0076 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0077 | 0/0 | 9536 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9531): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0078 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0079 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0080 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0081 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0082 | 0/0 | 9545 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0083 | 0/0 | 9539 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9534): Show |
chr2 | 163597611 | 163741008 |
a0001c0001t0084 | 0/0 | 9546 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0003 | 0/0 | 9537 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9532): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0004 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0007 | 0/0 | 9534 | 5 | 5 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9529): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0009 | 0/0 | 9542 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9537): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0011 | 0/0 | 9544 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0013 | 0/0 | 9546 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9541): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0016 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0001c0002t0028 | 0/0 | 9535 | 2 | 1 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9530): Show |
chr2 | 163597611 | 163741008 |
a0001c0003t0002 | 0/0 | 9545 | 2 | 0 | 0 | 2 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0003t0018 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0003t0032 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0003t0068 | 0/0 | 9545 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9540): Show |
chr2 | 163597611 | 163741008 |
a0001c0003t0085 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0004t0033 | 0/0 | 9541 | 2 | 0 | 2 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9536): Show |
chr2 | 163597611 | 163741008 |
a0001c0008t0035 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9539): Show |
chr2 | 163597611 | 163741008 |
a0001c0009t0005 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
a0002c0005t0054 | 0/0 | 9541 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9536): Show |
chr2 | 163597611 | 163741008 |
a0003c0006t0009 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9537): Show |
chr2 | 163597611 | 163741008 |
a0004c0007t0086 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | GTTTT others(9538): Show |
chr2 | 163597611 | 163741008 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0010g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0011g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0012g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0012g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0012g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0014g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0014g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0014g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0015g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0016g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0017g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0017g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0018g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0018g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0019g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0019g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0019g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0020g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0020g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0020g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0021g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0022g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0022g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0023g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0023g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0024g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0025g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0025g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0026g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0026g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0027g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0027g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0029g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0029g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0030g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0031g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0031g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0032g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0034g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0034g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0035g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0036g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0036g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0037g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0037g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0038g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0039g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0040g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0041g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0042g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0043g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0044g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0045g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0046g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0047g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0048g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0049g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0050g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0051g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0052g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0053g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0055g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0056g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0057g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0058g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0059g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0060g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0061g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0062g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0063g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0064g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0065g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0066g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0067g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0069g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0070g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0071g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0072g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0073g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0074g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0075g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0076g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0077g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0078g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0079g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0080g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0081g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0082g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0083g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0001t0084g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0016g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0016g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0028g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0002t0028g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0003t0018g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0003t0032g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0003t0068g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0003t0085g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0004t0033g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0004t0033g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0008t0035g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0001c0009t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0002c0005t0054g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0003c0006t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
a0004c0007t0086g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00323 | hp1 | a0001 | c0001 | t0082 | g0258 | EUR | FIN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00323 | hp2 | a0001 | c0001 | t0055 | g0044 | EUR | FIN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00408 | hp2 | a0001 | c0001 | t0052 | g0218 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00558 | hp1 | a0001 | c0001 | t0008 | g0168 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0222 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0069 | EAS | CHS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00639 | hp1 | a0001 | c0001 | t0077 | g0049 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00639 | hp2 | a0002 | c0005 | t0054 | g0017 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0062 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00735 | hp2 | a0001 | c0001 | t0011 | g0114 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG00741 | hp2 | a0001 | c0001 | t0083 | g0251 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01070 | hp1 | a0001 | c0004 | t0033 | g0138 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01070 | hp2 | a0001 | c0001 | t0019 | g0254 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01071 | hp1 | a0001 | c0004 | t0033 | g0175 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01175 | hp1 | a0001 | c0002 | t0028 | g0188 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01261 | hp1 | a0001 | c0001 | t0016 | g0130 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0170 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01358 | hp2 | a0001 | c0001 | t0037 | g0265 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01361 | hp2 | a0001 | c0001 | t0019 | g0261 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0154 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01433 | hp2 | a0001 | c0001 | t0019 | g0262 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01496 | hp1 | a0001 | c0001 | t0065 | g0156 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01496 | hp2 | a0001 | c0001 | t0023 | g0157 | AMR | CLM | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01515 | hp2 | a0001 | c0001 | t0067 | g0195 | EUR | IBS | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01884 | hp2 | a0001 | c0001 | t0081 | g0257 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01891 | hp1 | a0001 | c0001 | t0047 | g0186 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01978 | hp1 | a0001 | c0001 | t0022 | g0083 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02040 | hp1 | a0001 | c0001 | t0060 | g0059 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02056 | hp2 | a0001 | c0001 | t0074 | g0180 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02074 | hp1 | a0001 | c0001 | t0034 | g0255 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02129 | hp1 | a0001 | c0001 | t0064 | g0238 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02132 | hp2 | a0003 | c0006 | t0009 | g0217 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02135 | hp1 | a0001 | c0001 | t0022 | g0216 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02135 | hp2 | a0001 | c0001 | t0041 | g0030 | EAS | KHV | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CDX | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02257 | hp2 | a0001 | c0001 | t0071 | g0241 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02258 | hp1 | a0001 | c0001 | t0021 | g0243 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0182 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02280 | hp1 | a0001 | c0001 | t0056 | g0121 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02280 | hp2 | a0001 | c0001 | t0031 | g0131 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02293 | hp1 | a0001 | c0001 | t0023 | g0166 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02293 | hp2 | a0001 | c0001 | t0075 | g0009 | AMR | PEL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02451 | hp1 | a0001 | c0001 | t0026 | g0095 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02572 | hp1 | a0001 | c0002 | t0011 | g0129 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02630 | hp2 | a0001 | c0002 | t0007 | g0244 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02647 | hp1 | a0001 | c0002 | t0009 | g0120 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02647 | hp2 | a0001 | c0001 | t0026 | g0094 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02698 | hp1 | a0001 | c0001 | t0012 | g0071 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02723 | hp1 | a0001 | c0001 | t0045 | g0177 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02735 | hp1 | a0001 | c0001 | t0012 | g0145 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02735 | hp2 | a0001 | c0001 | t0012 | g0122 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02809 | hp1 | a0001 | c0001 | t0070 | g0103 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02886 | hp1 | a0001 | c0001 | t0013 | g0194 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02886 | hp2 | a0001 | c0002 | t0011 | g0092 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02895 | hp1 | a0001 | c0001 | t0015 | g0124 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02965 | hp2 | a0001 | c0002 | t0016 | g0067 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02970 | hp1 | a0001 | c0001 | t0059 | g0093 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02970 | hp2 | a0001 | c0001 | t0024 | g0001 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02976 | hp1 | a0001 | c0002 | t0007 | g0104 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0080 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0174 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03098 | hp1 | a0001 | c0002 | t0013 | g0191 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03130 | hp2 | a0001 | c0001 | t0030 | g0127 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03139 | hp1 | a0001 | c0001 | t0025 | g0109 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03195 | hp1 | a0001 | c0002 | t0007 | g0242 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0101 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03209 | hp2 | a0001 | c0001 | t0027 | g0107 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03225 | hp1 | a0001 | c0002 | t0007 | g0136 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03225 | hp2 | a0001 | c0001 | t0057 | g0108 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03453 | hp1 | a0001 | c0001 | t0021 | g0184 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03486 | hp1 | a0001 | c0002 | t0028 | g0134 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03491 | hp1 | a0001 | c0001 | t0012 | g0024 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03492 | hp1 | a0001 | c0001 | t0020 | g0256 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03540 | hp1 | a0001 | c0001 | t0072 | g0161 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03540 | hp2 | a0001 | c0001 | t0053 | g0125 | AFR | GWD | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03579 | hp1 | a0001 | c0002 | t0016 | g0132 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03579 | hp2 | a0001 | c0001 | t0030 | g0096 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03669 | hp2 | a0001 | c0001 | t0014 | g0025 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03688 | hp1 | a0001 | c0001 | t0014 | g0015 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03710 | hp1 | a0001 | c0001 | t0027 | g0167 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03710 | hp2 | a0001 | c0001 | t0069 | g0081 | SAS | PJL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03831 | hp1 | a0001 | c0001 | t0042 | g0178 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03831 | hp2 | a0001 | c0001 | t0049 | g0054 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03927 | hp2 | a0001 | c0001 | t0020 | g0247 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03942 | hp2 | a0001 | c0001 | t0038 | g0032 | SAS | BEB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0185 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18612 | hp1 | a0001 | c0001 | t0008 | g0060 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18612 | hp2 | a0001 | c0001 | t0018 | g0206 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18941 | hp1 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18943 | hp1 | a0001 | c0001 | t0044 | g0045 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18944 | hp1 | a0001 | c0001 | t0020 | g0263 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0181 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18959 | hp2 | a0001 | c0001 | t0079 | g0171 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18960 | hp1 | a0001 | c0001 | t0029 | g0022 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18960 | hp2 | a0001 | c0001 | t0010 | g0052 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18961 | hp1 | a0001 | c0001 | t0017 | g0147 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18961 | hp2 | a0004 | c0007 | t0086 | g0252 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18964 | hp1 | a0001 | c0001 | t0078 | g0057 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18964 | hp2 | a0001 | c0001 | t0034 | g0250 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18968 | hp1 | a0001 | c0001 | t0018 | g0027 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18973 | hp2 | a0001 | c0003 | t0002 | g0204 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18982 | hp1 | a0001 | c0001 | t0008 | g0072 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18982 | hp2 | a0001 | c0001 | t0043 | g0210 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18983 | hp1 | a0001 | c0001 | t0040 | g0211 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18983 | hp2 | a0001 | c0008 | t0035 | g0248 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18985 | hp1 | a0001 | c0001 | t0063 | g0234 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18985 | hp2 | a0001 | c0001 | t0010 | g0061 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18988 | hp2 | a0001 | c0003 | t0018 | g0224 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18991 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18993 | hp1 | a0001 | c0001 | t0035 | g0246 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18993 | hp2 | a0001 | c0003 | t0032 | g0086 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18994 | hp1 | a0001 | c0001 | t0080 | g0264 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18994 | hp2 | a0001 | c0001 | t0009 | g0063 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18995 | hp1 | a0001 | c0001 | t0048 | g0209 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18995 | hp2 | a0001 | c0001 | t0037 | g0259 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19000 | hp1 | a0001 | c0001 | t0051 | g0084 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19000 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19003 | hp1 | a0001 | c0003 | t0085 | g0260 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19004 | hp2 | a0001 | c0001 | t0014 | g0207 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19005 | hp1 | a0001 | c0001 | t0076 | g0068 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19006 | hp1 | a0001 | c0003 | t0068 | g0048 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19007 | hp1 | a0001 | c0001 | t0084 | g0253 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19009 | hp1 | a0001 | c0003 | t0002 | g0073 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19030 | hp1 | a0001 | c0001 | t0031 | g0091 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19043 | hp1 | a0001 | c0002 | t0003 | g0100 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19055 | hp2 | a0001 | c0001 | t0017 | g0151 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19056 | hp2 | a0001 | c0009 | t0005 | g0237 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19065 | hp1 | a0001 | c0001 | t0029 | g0215 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19065 | hp2 | a0001 | c0001 | t0066 | g0039 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19066 | hp1 | a0001 | c0001 | t0058 | g0155 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19066 | hp2 | a0001 | c0001 | t0036 | g0245 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19068 | hp2 | a0001 | c0001 | t0061 | g0149 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19070 | hp2 | a0001 | c0001 | t0017 | g0148 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19076 | hp1 | a0001 | c0001 | t0073 | g0011 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19076 | hp2 | a0001 | c0001 | t0062 | g0227 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19078 | hp1 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19078 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19079 | hp2 | a0001 | c0001 | t0036 | g0249 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19083 | hp1 | a0001 | c0001 | t0039 | g0231 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19083 | hp2 | a0001 | c0001 | t0032 | g0014 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA20129 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | ASW | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0173 | AFR | ASW | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02109 | hp2 | a0001 | c0001 | t0025 | g0230 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0126 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02486 | hp2 | a0001 | c0001 | t0046 | g0013 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG02559 | hp2 | a0001 | c0001 | t0050 | g0172 | AFR | ACB | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0123 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA20300 | hp1 | a0001 | c0002 | t0007 | g0135 | AFR | USA | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
NA20300 | hp2 | a0001 | c0001 | t0024 | g0001 | AFR | USA | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0113 | REF | REF | FIGN_chr2_163597611_163741008 | FIGN | chr2 | 163597611 | 163741008 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:163602611 | T | C | 1 | a0001 | 3 | HG02886.hp1 HG03098.hp1 HG03209.hp1 |
splice_region_variant | LOW | c.*6941A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | chr2 | 163602611 | |||||||
chr2:163609662 | C | T | 1 | a0003 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.2170G>A | p.Val724Ile | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2486/9537 | 2170/2280 | 724/759 | chr2 | 163609662 | |||
chr2:163610148 | C | T | 1 | a0002 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1684G>A | p.Glu562Lys | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2000/9537 | 1684/2280 | 562/759 | chr2 | 163610148 | |||
chr2:163610300 | G | A | 1 | a0004 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.1532C>T | p.Ala511Val | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1848/9537 | 1532/2280 | 511/759 | chr2 | 163610300 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:163609663 | G | A | 1 | a0001c0003 | 6 | NA18973.hp2 NA18988.hp2 NA18993.hp2 others(3): Show |
synonymous_variant | LOW | c.2169C>T | p.Pro723Pro | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2485/9537 | 2169/2280 | 723/759 | chr2 | 163609663 | |||
chr2:163609720 | G | A | 1 | a0001c0004 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.2112C>T | p.Pro704Pro | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2428/9537 | 2112/2280 | 704/759 | chr2 | 163609720 | |||
chr2:163610977 | T | A | 1 | a0001c0002 | 15 | HG01175.hp1 HG02572.hp1 HG02630.hp2 others(12): Show |
synonymous_variant | LOW | c.855A>T | p.Leu285Leu | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1171/9537 | 855/2280 | 285/759 | chr2 | 163610977 | |||
chr2:163611511 | T | C | 1 | a0001c0008 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.321A>G | p.Glu107Glu | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 637/9537 | 321/2280 | 107/759 | chr2 | 163611511 | |||
chr2:163611685 | G | C | 1 | a0001c0009 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.147C>G | p.Thr49Thr | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 463/9537 | 147/2280 | 49/759 | chr2 | 163611685 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:163602871 | A | G | 9 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0038 others(6): Show |
14 | HG00323.hp1 HG02559.hp2 HG02698.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6681T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6681 | chr2 | 163602871 | ||||||
chr2:163602880 | T | A | 2 | a0001c0001t0025 a0001c0001t0031 |
4 | HG02109.hp2 HG02280.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6672A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6672 | chr2 | 163602880 | ||||||
chr2:163602912 | G | T | 32 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(29): Show |
76 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*6640C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6640 | chr2 | 163602912 | ||||||
chr2:163603217 | A | T | 2 | a0001c0001t0032 a0001c0003t0032 |
2 | NA18993.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6335T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6335 | chr2 | 163603217 | ||||||
chr2:163603432 | C | G | 1 | a0001c0001t0026 | 2 | HG02451.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6120G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 6120 | chr2 | 163603432 | ||||||
chr2:163603706 | A | C | 1 | a0001c0001t0066 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5846T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5846 | chr2 | 163603706 | ||||||
chr2:163604118 | A | G | 2 | a0001c0001t0055 a0002c0005t0054 |
2 | HG00323.hp2 HG00639.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5434T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5434 | chr2 | 163604118 | ||||||
chr2:163604247 | T | G | 1 | a0001c0001t0064 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5305A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5305 | chr2 | 163604247 | ||||||
chr2:163604367 | G | A | 4 | a0001c0001t0055 a0001c0001t0056 a0001c0001t0057 others(1): Show |
4 | HG00323.hp2 HG00639.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5185C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5185 | chr2 | 163604367 | ||||||
chr2:163604437 | A | G | 34 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(31): Show |
78 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5115T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 5115 | chr2 | 163604437 | ||||||
chr2:163604659 | T | C | 1 | a0002c0005t0054 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4893A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4893 | chr2 | 163604659 | ||||||
chr2:163604802 | C | CAG | 32 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(29): Show |
76 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*4748_*4749dupCT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4749 | chr2 | 163604802 | ||||||
chr2:163604802 | C | CAGAG | 5 | a0001c0001t0055 a0001c0001t0059 a0001c0001t0063 others(2): Show |
5 | HG00323.hp2 HG00639.hp2 HG00741.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4746_*4749dupCTCT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4749 | chr2 | 163604802 | ||||||
chr2:163604849 | G | A | 1 | a0001c0001t0065 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4703C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4703 | chr2 | 163604849 | ||||||
chr2:163604936 | C | CTTTTT | 16 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0015 others(13): Show |
28 | HG00323.hp2 HG00639.hp2 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4611_*4615dupAAAA others(1): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | ||||||
chr2:163604936 | C | CTTTTTT | 16 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(13): Show |
28 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4610_*4615dupAAAA others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | ||||||
chr2:163604936 | C | CTTTTTTT | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
137 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*4609_*4615dupAAAA others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | ||||||
chr2:163604936 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0037 others(5): Show |
22 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4608_*4615dupAAAA others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | ||||||
chr2:163604936 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0038 others(4): Show |
12 | HG00323.hp1 HG02698.hp1 HG02735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4607_*4615dupAAAA others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | ||||||
chr2:163604936 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0048 a0001c0001t0049 a0001c0001t0058 |
3 | HG03831.hp2 NA18995.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4606_*4615dupAAAA others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | ||||||
chr2:163604936 | CT | C | 4 | a0001c0001t0067 a0001c0001t0077 a0001c0001t0083 others(1): Show |
5 | HG00639.hp1 HG00741.hp2 HG01175.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4615delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4615 | chr2 | 163604936 | ||||||
chr2:163604936 | CTT | C | 2 | a0001c0001t0007 a0001c0002t0007 |
7 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4614_*4615delAA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4614 | chr2 | 163604936 | ||||||
chr2:163604984 | T | C | 9 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0026 others(6): Show |
18 | HG00323.hp2 HG00639.hp2 HG01175.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4568A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4568 | chr2 | 163604984 | ||||||
chr2:163605443 | G | A | 1 | a0001c0001t0074 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4109C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4109 | chr2 | 163605443 | ||||||
chr2:163605454 | A | C | 1 | a0001c0001t0059 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4098T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4098 | chr2 | 163605454 | ||||||
chr2:163605488 | A | G | 1 | a0001c0001t0055 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4064T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 4064 | chr2 | 163605488 | ||||||
chr2:163605695 | G | A | 1 | a0001c0003t0068 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3857C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3857 | chr2 | 163605695 | ||||||
chr2:163605897 | AT | A | 44 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(41): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3654delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3654 | chr2 | 163605897 | ||||||
chr2:163605897 | ATT | A | 2 | a0001c0001t0012 a0001c0001t0049 |
5 | HG02698.hp1 HG02735.hp1 HG02735.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3653_*3654delAA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3653 | chr2 | 163605897 | ||||||
chr2:163605931 | C | T | 1 | a0001c0001t0026 | 2 | HG02451.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3621G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3621 | chr2 | 163605931 | ||||||
chr2:163606014 | T | C | 1 | a0001c0001t0075 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3538A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3538 | chr2 | 163606014 | ||||||
chr2:163606145 | A | T | 1 | a0001c0001t0062 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3407T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3407 | chr2 | 163606145 | ||||||
chr2:163606168 | C | T | 1 | a0001c0001t0030 | 2 | HG03130.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3384G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3384 | chr2 | 163606168 | ||||||
chr2:163606297 | A | G | 2 | a0001c0001t0043 a0001c0001t0080 |
2 | NA18982.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3255T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 3255 | chr2 | 163606297 | ||||||
chr2:163606611 | C | G | 1 | a0002c0005t0054 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2941G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2941 | chr2 | 163606611 | ||||||
chr2:163606623 | C | T | 2 | a0001c0001t0017 a0001c0001t0061 |
4 | NA18961.hp1 NA19055.hp2 NA19068.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2929G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2929 | chr2 | 163606623 | ||||||
chr2:163606782 | T | C | 1 | a0001c0001t0050 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2770A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2770 | chr2 | 163606782 | ||||||
chr2:163606904 | A | T | 2 | a0001c0001t0035 a0001c0008t0035 |
2 | NA18983.hp2 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2648T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2648 | chr2 | 163606904 | ||||||
chr2:163606976 | T | A | 31 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(28): Show |
75 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2576A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2576 | chr2 | 163606976 | ||||||
chr2:163606981 | G | A | 7 | a0001c0001t0009 a0001c0001t0030 a0001c0001t0034 others(4): Show |
12 | HG01070.hp1 HG01071.hp1 HG02074.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2571C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2571 | chr2 | 163606981 | ||||||
chr2:163607131 | C | T | 1 | a0001c0001t0069 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2421G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2421 | chr2 | 163607131 | ||||||
chr2:163607528 | CTATGT | C | 4 | a0001c0001t0055 a0001c0001t0056 a0001c0001t0057 others(1): Show |
4 | HG00323.hp2 HG00639.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2019_*2023delACAT others(1): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2019 | chr2 | 163607528 | ||||||
chr2:163607546 | A | G | 27 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0011 others(24): Show |
96 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2006T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 2006 | chr2 | 163607546 | ||||||
chr2:163607588 | G | GA | 3 | a0001c0001t0011 a0001c0001t0045 a0001c0002t0011 |
6 | HG00735.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1963dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1963 | chr2 | 163607588 | ||||||
chr2:163607593 | A | C | 1 | a0001c0004t0033 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1959T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1959 | chr2 | 163607593 | ||||||
chr2:163607647 | T | A | 1 | a0001c0001t0059 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1905A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1905 | chr2 | 163607647 | ||||||
chr2:163607722 | A | C | 2 | a0001c0001t0025 a0001c0001t0031 |
4 | HG02109.hp2 HG02280.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1830T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1830 | chr2 | 163607722 | ||||||
chr2:163608027 | T | C | 1 | a0001c0001t0031 | 2 | HG02280.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1525A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1525 | chr2 | 163608027 | ||||||
chr2:163608045 | T | C | 2 | a0001c0001t0046 a0001c0001t0081 |
2 | HG01884.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1507A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1507 | chr2 | 163608045 | ||||||
chr2:163608087 | T | C | 1 | a0001c0001t0058 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1465A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1465 | chr2 | 163608087 | ||||||
chr2:163608256 | G | GAT | 3 | a0001c0001t0013 a0001c0001t0047 a0001c0002t0013 |
4 | HG01891.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1294_*1295dupAT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1295 | chr2 | 163608256 | ||||||
chr2:163608267 | G | A | 61 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(58): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1285C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 1285 | chr2 | 163608267 | ||||||
chr2:163608793 | G | T | 1 | a0001c0001t0038 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*759C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 759 | chr2 | 163608793 | ||||||
chr2:163608842 | T | A | 1 | a0001c0001t0059 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*710A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 710 | chr2 | 163608842 | ||||||
chr2:163609119 | T | C | 1 | a0001c0001t0078 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*433A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 433 | chr2 | 163609119 | ||||||
chr2:163609206 | G | A | 23 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(20): Show |
63 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*346C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 346 | chr2 | 163609206 | ||||||
chr2:163609522 | T | C | 2 | a0001c0001t0079 a0004c0007t0086 |
2 | NA18959.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*30A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 30 | chr2 | 163609522 | ||||||
chr2:163609529 | AT | A | 19 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0011 others(16): Show |
87 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*22delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 3/3 | 22 | chr2 | 163609529 | ||||||
chr2:163735859 | C | T | 14 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0034 others(11): Show |
21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-167G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/3 | 932 | chr2 | 163735859 | ||||||
chr2:163735905 | G | C | 14 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0034 others(11): Show |
21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-213C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/3 | chr2 | 163735905 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:163611818 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-12C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611818 | |||||||
chr2:163611824 | A | G | 1 | a0001c0001t0025g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-18T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611824 | |||||||
chr2:163611850 | A | G | 106 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(103): Show |
106 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.26-44T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611850 | |||||||
chr2:163611904 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
83 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-98A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611904 | |||||||
chr2:163611933 | C | T | 3 | a0001c0001t0002g0050 a0001c0001t0004g0036 a0001c0001t0004g0225 |
3 | NA18955.hp1 NA18977.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.26-127G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611933 | |||||||
chr2:163611951 | T | C | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26-145A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163611951 | |||||||
chr2:163612046 | A | G | 1 | a0001c0001t0004g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-240T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612046 | |||||||
chr2:163612096 | T | A | 21 | a0001c0001t0001g0110 a0001c0001t0001g0119 a0001c0001t0001g0176 others(18): Show |
21 | HG00323.hp1 HG01106.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.26-290A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612096 | |||||||
chr2:163612317 | C | A | 2 | a0001c0004t0033g0138 a0001c0004t0033g0175 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.26-511G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612317 | |||||||
chr2:163612587 | G | GA | 22 | a0001c0001t0001g0016 a0001c0001t0001g0055 a0001c0001t0001g0077 others(19): Show |
23 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.26-782dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612587 | |||||||
chr2:163612665 | C | T | 1 | a0001c0001t0047g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.26-859G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612665 | |||||||
chr2:163612676 | G | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
83 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-870C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612676 | |||||||
chr2:163612692 | A | ATG | 85 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0056 others(82): Show |
85 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-888_26-887dupCA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | |||||||
chr2:163612692 | A | ATGTG | 61 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(58): Show |
61 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.26-890_26-887dupCA others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | |||||||
chr2:163612692 | A | ATGTGTG | 12 | a0001c0001t0001g0119 a0001c0001t0002g0208 a0001c0001t0003g0097 others(9): Show |
13 | HG01261.hp1 HG01496.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-892_26-887dupCA others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | |||||||
chr2:163612692 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0077 a0001c0001t0009g0063 a0001c0001t0034g0250 others(2): Show |
5 | HG02559.hp2 HG03579.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-894_26-887dupCA others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | |||||||
chr2:163612692 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0057g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-896_26-887dupCA others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612692 | |||||||
chr2:163612749 | C | CAT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0003g0240 others(4): Show |
7 | HG00639.hp2 HG01257.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-945_26-944dupAT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612749 | |||||||
chr2:163612749 | CAT | C | 130 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(127): Show |
131 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.26-945_26-944delAT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612749 | |||||||
chr2:163612749 | CATAT | C | 19 | a0001c0001t0001g0110 a0001c0001t0001g0119 a0001c0001t0001g0143 others(16): Show |
19 | HG00140.hp1 HG00323.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-947_26-944delAT others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612749 | |||||||
chr2:163612785 | A | AAG | 117 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(114): Show |
117 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.26-981_26-980dupCT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612785 | |||||||
chr2:163612849 | T | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(26): Show |
29 | HG00408.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.26-1043A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612849 | |||||||
chr2:163612853 | T | C | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | NA18943.hp2 NA18959.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-1047A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163612853 | |||||||
chr2:163613126 | C | T | 1 | a0001c0001t0071g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-1320G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163613126 | |||||||
chr2:163613534 | C | T | 57 | a0001c0001t0001g0056 a0001c0001t0001g0141 a0001c0001t0001g0143 others(54): Show |
57 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.26-1728G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163613534 | |||||||
chr2:163613602 | G | A | 1 | a0001c0001t0022g0216 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.26-1796C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163613602 | |||||||
chr2:163614238 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-2432T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614238 | |||||||
chr2:163614353 | C | A | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-2547G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614353 | |||||||
chr2:163614467 | T | G | 23 | a0001c0001t0001g0016 a0001c0001t0001g0055 a0001c0001t0001g0077 others(20): Show |
24 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.26-2661A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614467 | |||||||
chr2:163614634 | C | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
89 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.26-2828G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614634 | |||||||
chr2:163614686 | G | A | 22 | a0001c0001t0001g0016 a0001c0001t0001g0055 a0001c0001t0001g0077 others(19): Show |
23 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.26-2880C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614686 | |||||||
chr2:163614709 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.26-2903G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614709 | |||||||
chr2:163614823 | T | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
89 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.26-3017A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614823 | |||||||
chr2:163614833 | CAGG | C | 3 | a0001c0001t0001g0143 a0001c0001t0002g0144 a0001c0001t0005g0179 |
3 | NA18945.hp2 NA18969.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.26-3030_26-3028del others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614833 | |||||||
chr2:163614870 | A | T | 63 | a0001c0001t0001g0056 a0001c0001t0001g0141 a0001c0001t0001g0143 others(60): Show |
63 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-3064T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614870 | |||||||
chr2:163614912 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.26-3106T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614912 | |||||||
chr2:163614922 | A | G | 1 | a0001c0001t0004g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-3116T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614922 | |||||||
chr2:163614948 | G | A | 1 | a0001c0001t0050g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-3142C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163614948 | |||||||
chr2:163615046 | A | T | 5 | a0001c0001t0021g0184 a0001c0001t0021g0243 a0001c0001t0025g0109 others(2): Show |
5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-3240T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615046 | |||||||
chr2:163615077 | T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-3271A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615077 | |||||||
chr2:163615216 | A | G | 5 | a0001c0001t0021g0184 a0001c0001t0021g0243 a0001c0001t0025g0109 others(2): Show |
5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-3410T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615216 | |||||||
chr2:163615345 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.26-3539A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615345 | |||||||
chr2:163615475 | A | T | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-3669T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615475 | |||||||
chr2:163615578 | T | A | 2 | a0001c0001t0070g0103 a0001c0002t0007g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-3772A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615578 | |||||||
chr2:163615595 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(186): Show |
189 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.26-3789A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615595 | |||||||
chr2:163615764 | T | A | 17 | a0001c0001t0001g0110 a0001c0001t0001g0119 a0001c0001t0001g0163 others(14): Show |
17 | HG00140.hp1 HG00323.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-3958A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615764 | |||||||
chr2:163615912 | A | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0082 others(6): Show |
9 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-4106T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163615912 | |||||||
chr2:163616058 | GT | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0082 others(6): Show |
9 | HG00741.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-4253delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616058 | |||||||
chr2:163616060 | A | G | 66 | a0001c0001t0001g0056 a0001c0001t0001g0141 a0001c0001t0001g0143 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.26-4254T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616060 | |||||||
chr2:163616139 | A | G | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.26-4333T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616139 | |||||||
chr2:163616726 | G | C | 1 | a0001c0001t0004g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-4920C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616726 | |||||||
chr2:163616936 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(232): Show |
236 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.26-5130T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163616936 | |||||||
chr2:163617007 | G | A | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.26-5201C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617007 | |||||||
chr2:163617149 | C | T | 3 | a0001c0001t0003g0097 a0001c0001t0013g0194 a0001c0001t0031g0131 |
3 | HG02280.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.26-5343G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617149 | |||||||
chr2:163617243 | A | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
85 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-5437T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617243 | |||||||
chr2:163617371 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0077 a0001c0001t0014g0025 |
3 | HG03669.hp2 HG03927.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.26-5565A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617371 | |||||||
chr2:163617712 | T | C | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-5906A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617712 | |||||||
chr2:163617714 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26-5908C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617714 | |||||||
chr2:163617759 | A | C | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-5953T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163617759 | |||||||
chr2:163618127 | G | C | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-6321C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618127 | |||||||
chr2:163618414 | C | CT | 39 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(36): Show |
39 | HG00408.hp1 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.26-6609dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618414 | |||||||
chr2:163618414 | CT | C | 6 | a0001c0001t0001g0143 a0001c0001t0002g0005 a0001c0001t0002g0075 others(3): Show |
6 | NA18945.hp2 NA18946.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-6609delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618414 | |||||||
chr2:163618680 | T | C | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-6874A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163618680 | |||||||
chr2:163619171 | A | G | 1 | a0001c0001t0063g0234 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.26-7365T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619171 | |||||||
chr2:163619313 | T | G | 1 | a0001c0001t0003g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-7507A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619313 | |||||||
chr2:163619448 | C | T | 1 | a0001c0001t0010g0214 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.26-7642G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619448 | |||||||
chr2:163619576 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-7770C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619576 | |||||||
chr2:163619805 | T | A | 1 | a0001c0001t0015g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.26-7999A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619805 | |||||||
chr2:163619854 | A | T | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-8048T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619854 | |||||||
chr2:163619980 | A | T | 2 | a0001c0001t0019g0254 a0001c0001t0027g0167 |
2 | HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.26-8174T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619980 | |||||||
chr2:163619984 | A | G | 1 | a0001c0002t0016g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.26-8178T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163619984 | |||||||
chr2:163620036 | T | A | 1 | a0001c0001t0061g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.26-8230A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620036 | |||||||
chr2:163620266 | C | T | 1 | a0001c0001t0082g0258 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-8460G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620266 | |||||||
chr2:163620377 | G | T | 1 | a0001c0001t0013g0101 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.26-8571C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620377 | |||||||
chr2:163620407 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.26-8601A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620407 | |||||||
chr2:163620590 | T | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(227): Show |
231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.26-8784A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620590 | |||||||
chr2:163620705 | C | T | 1 | a0001c0001t0022g0216 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.26-8899G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620705 | |||||||
chr2:163620851 | T | TTG | 53 | a0001c0001t0001g0056 a0001c0001t0001g0119 a0001c0001t0001g0140 others(50): Show |
53 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.26-9047_26-9046dup others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620851 | T | TTGTG | 29 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(26): Show |
29 | HG00408.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.26-9049_26-9046dup others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620851 | T | TTGTGTG | 28 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0053 others(25): Show |
28 | HG00140.hp1 HG01106.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.26-9051_26-9046dup others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620851 | T | TTGTGTGT others(1): Show |
18 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0003g0183 others(15): Show |
18 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.26-9053_26-9046dup others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620851 | T | TTGTGTGT others(3): Show |
63 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0021 others(60): Show |
63 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-9055_26-9046dup others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620851 | T | TTGTGTGT others(5): Show |
7 | a0001c0001t0002g0088 a0001c0001t0005g0080 a0001c0001t0008g0072 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-9057_26-9046dup others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620851 | TTG | T | 2 | a0001c0001t0004g0192 a0001c0001t0024g0001 |
3 | HG02970.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-9047_26-9046del others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620851 | TTGTG | T | 24 | a0001c0001t0001g0016 a0001c0001t0001g0055 a0001c0001t0001g0077 others(21): Show |
24 | HG00558.hp1 HG01070.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.26-9049_26-9046del others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620851 | |||||||
chr2:163620879 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0076g0068 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.26-9074_26-9073ins others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163620879 | |||||||
chr2:163621211 | A | G | 1 | a0001c0001t0057g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-9405T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621211 | |||||||
chr2:163621262 | G | A | 96 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0110 others(93): Show |
96 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.26-9456C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621262 | |||||||
chr2:163621268 | T | C | 5 | a0001c0001t0015g0123 a0001c0001t0015g0124 a0001c0001t0015g0126 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-9462A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621268 | |||||||
chr2:163621341 | C | T | 136 | a0001c0001t0001g0016 a0001c0001t0001g0031 a0001c0001t0001g0043 others(133): Show |
137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.26-9535G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621341 | |||||||
chr2:163621901 | G | A | 10 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0002g0004 others(7): Show |
10 | HG02027.hp1 NA18612.hp2 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-10095C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621901 | |||||||
chr2:163621926 | C | T | 1 | a0001c0001t0081g0257 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26-10120G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163621926 | |||||||
chr2:163622137 | G | A | 1 | a0001c0002t0007g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.26-10331C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622137 | |||||||
chr2:163622287 | A | G | 1 | a0001c0001t0048g0209 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.26-10481T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622287 | |||||||
chr2:163622319 | G | A | 6 | a0001c0001t0017g0147 a0001c0001t0017g0148 a0001c0001t0017g0151 others(3): Show |
6 | NA18959.hp2 NA18961.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-10513C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622319 | |||||||
chr2:163622334 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0031g0091 a0001c0001t0059g0093 |
3 | HG02970.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26-10528T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622334 | |||||||
chr2:163622358 | G | T | 8 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0015g0126 others(5): Show |
8 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-10552C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622358 | |||||||
chr2:163622441 | C | T | 10 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0005g0159 others(7): Show |
10 | HG00408.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-10635G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622441 | |||||||
chr2:163622618 | G | T | 6 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0021g0243 others(3): Show |
6 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-10812C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622618 | |||||||
chr2:163622699 | C | T | 1 | a0001c0001t0005g0033 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.26-10893G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622699 | |||||||
chr2:163622776 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.26-10970C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622776 | |||||||
chr2:163622921 | A | C | 2 | a0001c0001t0001g0228 a0001c0001t0002g0089 |
2 | HG02056.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.26-11115T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163622921 | |||||||
chr2:163623271 | A | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.26-11465T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623271 | |||||||
chr2:163623291 | A | C | 3 | a0001c0001t0005g0033 a0001c0001t0035g0246 a0001c0008t0035g0248 |
3 | HG00408.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-11485T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623291 | |||||||
chr2:163623334 | T | C | 15 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0005g0159 others(12): Show |
15 | HG00408.hp1 HG00558.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-11528A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623334 | |||||||
chr2:163623397 | T | C | 1 | a0001c0001t0021g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.26-11591A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623397 | |||||||
chr2:163623447 | C | T | 20 | a0001c0001t0001g0118 a0001c0001t0001g0219 a0001c0001t0003g0187 others(17): Show |
20 | HG00735.hp2 HG01175.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.26-11641G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623447 | |||||||
chr2:163623570 | T | C | 1 | a0001c0001t0006g0023 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.26-11764A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623570 | |||||||
chr2:163623808 | C | T | 5 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0029g0215 others(2): Show |
5 | HG00558.hp1 HG03942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-12002G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623808 | |||||||
chr2:163623869 | T | C | 8 | a0001c0001t0001g0111 a0001c0001t0001g0152 a0001c0001t0001g0164 others(5): Show |
8 | HG00140.hp2 HG01070.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-12063A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623869 | |||||||
chr2:163623935 | C | T | 2 | a0001c0001t0011g0114 a0001c0001t0011g0189 |
2 | HG00735.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.26-12129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163623935 | |||||||
chr2:163624065 | TTGATA | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
100 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.26-12264_26-12260d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624065 | |||||||
chr2:163624119 | C | G | 5 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0014g0015 others(2): Show |
5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-12313G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624119 | |||||||
chr2:163624179 | T | C | 2 | a0001c0001t0050g0172 a0001c0001t0057g0108 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-12373A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624179 | |||||||
chr2:163624691 | C | CAT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.26-12887_26-12886d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624691 | |||||||
chr2:163624691 | C | CATAT | 13 | a0001c0001t0001g0141 a0001c0001t0002g0004 a0001c0001t0003g0240 others(10): Show |
13 | HG01261.hp1 HG01891.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-12889_26-12886d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624691 | |||||||
chr2:163624691 | C | CATATAT | 5 | a0001c0001t0011g0114 a0001c0001t0011g0189 a0001c0001t0013g0101 others(2): Show |
5 | HG00735.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-12891_26-12886d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624691 | |||||||
chr2:163624708 | A | ATAT | 6 | a0001c0001t0002g0074 a0001c0001t0006g0239 a0001c0001t0018g0027 others(3): Show |
6 | HG01175.hp1 HG02074.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-12903_26-12902i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624708 | |||||||
chr2:163624708 | A | T | 5 | a0001c0001t0001g0176 a0001c0001t0003g0193 a0001c0001t0005g0159 others(2): Show |
5 | HG01106.hp1 HG01515.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-12902T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624708 | |||||||
chr2:163624708 | AT | A | 7 | a0001c0001t0001g0119 a0001c0001t0007g0020 a0001c0001t0047g0186 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-12903delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624708 | |||||||
chr2:163624709 | T | TA | 24 | a0001c0001t0001g0112 a0001c0001t0001g0220 a0001c0001t0002g0146 others(21): Show |
24 | HG00323.hp1 HG00609.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-12904_26-12903i others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624709 | |||||||
chr2:163624709 | T | TATA | 49 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0140 others(46): Show |
49 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.26-12904_26-12903i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624709 | |||||||
chr2:163624710 | T | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(103): Show |
106 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.26-12904A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624710 | |||||||
chr2:163624711 | T | A | 3 | a0001c0001t0002g0026 a0001c0001t0074g0180 a0001c0002t0009g0120 |
3 | HG02056.hp2 HG02132.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.26-12905A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624711 | |||||||
chr2:163624712 | T | A | 4 | a0001c0001t0005g0033 a0001c0001t0006g0023 a0001c0001t0009g0128 others(1): Show |
4 | HG00408.hp1 HG02257.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-12906A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624712 | |||||||
chr2:163624922 | T | C | 1 | a0001c0001t0020g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.26-13116A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624922 | |||||||
chr2:163624951 | A | G | 1 | a0001c0001t0003g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.26-13145T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624951 | |||||||
chr2:163624978 | G | T | 1 | a0001c0001t0018g0206 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.26-13172C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624978 | |||||||
chr2:163624996 | C | A | 3 | a0001c0001t0004g0192 a0001c0001t0007g0020 a0001c0002t0011g0092 |
3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-13190G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163624996 | |||||||
chr2:163625129 | C | T | 9 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0015g0126 others(6): Show |
9 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-13323G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625129 | |||||||
chr2:163625227 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0077 |
2 | HG01167.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.26-13421T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625227 | |||||||
chr2:163625257 | C | A | 2 | a0001c0001t0050g0172 a0001c0001t0057g0108 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-13451G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625257 | |||||||
chr2:163625278 | G | C | 1 | a0001c0001t0005g0179 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.26-13472C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625278 | |||||||
chr2:163625358 | A | G | 46 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(43): Show |
47 | HG00558.hp1 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-13552T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625358 | |||||||
chr2:163625427 | T | C | 2 | a0001c0001t0029g0022 a0001c0001t0051g0084 |
2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-13621A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625427 | |||||||
chr2:163625458 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0014g0025 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26-13652A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625458 | |||||||
chr2:163625489 | G | A | 1 | a0001c0001t0050g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-13683C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625489 | |||||||
chr2:163625632 | A | G | 13 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0005g0159 others(10): Show |
13 | HG00408.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-13826T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625632 | |||||||
chr2:163625936 | A | C | 1 | a0001c0001t0043g0210 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.26-14130T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163625936 | |||||||
chr2:163626179 | A | G | 6 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0014g0015 others(3): Show |
6 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-14373T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626179 | |||||||
chr2:163626204 | TC | T | 3 | a0001c0001t0005g0033 a0001c0001t0035g0246 a0001c0008t0035g0248 |
3 | HG00408.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-14399delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626204 | |||||||
chr2:163626421 | A | G | 1 | a0001c0003t0002g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.26-14615T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626421 | |||||||
chr2:163626779 | C | G | 1 | a0001c0001t0060g0059 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-14973G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626779 | |||||||
chr2:163626819 | C | T | 2 | a0001c0001t0005g0153 a0001c0001t0005g0160 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-15013G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626819 | |||||||
chr2:163626878 | C | T | 1 | a0001c0001t0058g0155 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.26-15072G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626878 | |||||||
chr2:163626953 | G | A | 17 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(14): Show |
17 | HG01175.hp1 HG02040.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-15147C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626953 | |||||||
chr2:163626973 | A | G | 21 | a0001c0001t0002g0019 a0001c0001t0003g0106 a0001c0001t0005g0033 others(18): Show |
21 | HG00408.hp1 HG00558.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.26-15167T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163626973 | |||||||
chr2:163627062 | G | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.26-15256C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627062 | |||||||
chr2:163627445 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(105): Show |
108 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.26-15639A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627445 | |||||||
chr2:163627610 | C | A | 5 | a0001c0001t0001g0220 a0001c0001t0025g0230 a0001c0002t0007g0135 others(2): Show |
5 | HG02109.hp2 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-15804G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627610 | |||||||
chr2:163627693 | C | G | 17 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(14): Show |
17 | HG01175.hp1 HG02040.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-15887G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627693 | |||||||
chr2:163627796 | T | C | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.26-15990A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627796 | |||||||
chr2:163627838 | T | TTGAAGGC others(6): Show |
1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-16045_26-16033d others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163627838 | |||||||
chr2:163628248 | TG | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(65): Show |
69 | HG00408.hp1 HG00558.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.26-16443delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628248 | |||||||
chr2:163628649 | T | A | 1 | a0001c0001t0057g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-16843A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628649 | |||||||
chr2:163628761 | A | T | 1 | a0001c0001t0007g0182 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26-16955T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628761 | |||||||
chr2:163628923 | T | A | 5 | a0001c0001t0013g0101 a0001c0001t0021g0243 a0001c0001t0025g0109 others(2): Show |
5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-17117A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163628923 | |||||||
chr2:163629038 | G | A | 1 | a0001c0001t0050g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.26-17232C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629038 | |||||||
chr2:163629087 | C | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(65): Show |
69 | HG00408.hp1 HG00558.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.26-17281G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629087 | |||||||
chr2:163629344 | A | G | 1 | a0001c0001t0045g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.26-17538T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629344 | |||||||
chr2:163629455 | G | T | 11 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0015g0123 others(8): Show |
11 | HG00558.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-17649C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629455 | |||||||
chr2:163629952 | C | CT | 56 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0043 others(53): Show |
57 | HG00735.hp2 HG00741.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.26-18147dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | C | CTT | 9 | a0001c0001t0001g0012 a0001c0001t0003g0187 a0001c0001t0006g0006 others(6): Show |
9 | HG00735.hp1 HG01167.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-18148_26-18147d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0015g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.26-18159_26-18147d others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0015g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.26-18160_26-18147d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | CT | C | 29 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0078 others(26): Show |
29 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.26-18147delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | CTT | C | 5 | a0001c0001t0001g0169 a0001c0001t0003g0240 a0001c0001t0050g0172 others(2): Show |
5 | HG00140.hp2 HG01891.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-18148_26-18147d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | CTTTT | C | 5 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0029g0215 others(2): Show |
5 | HG00558.hp1 HG03942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-18150_26-18147d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0014g0015 others(2): Show |
5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-18154_26-18147d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-18156_26-18147d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-18160_26-18147d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163629952 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0021g0184 a0001c0001t0056g0121 |
2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-18164_26-18147d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163629952 | |||||||
chr2:163630036 | C | T | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-18230G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630036 | |||||||
chr2:163630043 | C | T | 1 | a0001c0001t0007g0182 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26-18237G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630043 | |||||||
chr2:163630118 | C | A | 11 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0015g0123 others(8): Show |
11 | HG00558.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-18312G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630118 | |||||||
chr2:163630129 | C | A | 2 | a0001c0001t0019g0254 a0001c0001t0027g0167 |
2 | HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.26-18323G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630129 | |||||||
chr2:163630328 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0011g0114 a0001c0001t0011g0189 others(1): Show |
4 | HG00735.hp2 HG02723.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-18522A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630328 | |||||||
chr2:163630339 | T | C | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.26-18533A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630339 | |||||||
chr2:163630349 | T | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0150 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.26-18543A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630349 | |||||||
chr2:163630369 | G | A | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-18563C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630369 | |||||||
chr2:163630510 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(127): Show |
130 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.26-18704G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630510 | |||||||
chr2:163630573 | C | T | 2 | a0001c0001t0036g0245 a0004c0007t0086g0252 |
2 | NA18961.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.26-18767G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630573 | |||||||
chr2:163630675 | A | AG | 51 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(48): Show |
52 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.26-18870dupC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630675 | |||||||
chr2:163630683 | G | T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-18877C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630683 | |||||||
chr2:163630938 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0014g0025 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26-19132G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163630938 | |||||||
chr2:163631060 | G | A | 2 | a0001c0001t0050g0172 a0001c0001t0057g0108 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-19254C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631060 | |||||||
chr2:163631374 | C | T | 2 | a0001c0004t0033g0138 a0001c0004t0033g0175 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.26-19568G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631374 | |||||||
chr2:163631504 | T | C | 1 | a0001c0001t0003g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-19698A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631504 | |||||||
chr2:163631733 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(30): Show |
34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-19927T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631733 | |||||||
chr2:163631865 | A | C | 9 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(6): Show |
9 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-20059T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631865 | |||||||
chr2:163631883 | C | T | 2 | a0001c0001t0021g0243 a0001c0002t0007g0242 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.26-20077G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163631883 | |||||||
chr2:163632016 | C | T | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-20210G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632016 | |||||||
chr2:163632031 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(178): Show |
182 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.26-20225G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632031 | |||||||
chr2:163632299 | G | A | 1 | a0001c0001t0020g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.26-20493C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632299 | |||||||
chr2:163632425 | G | T | 1 | a0001c0003t0002g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.26-20619C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632425 | |||||||
chr2:163632504 | T | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(30): Show |
34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-20698A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632504 | |||||||
chr2:163632556 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20750G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632556 | |||||||
chr2:163632565 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20759A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632565 | |||||||
chr2:163632586 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20780T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632586 | |||||||
chr2:163632590 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20784T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632590 | |||||||
chr2:163632592 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20786A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632592 | |||||||
chr2:163632594 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20788G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632594 | |||||||
chr2:163632595 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20789T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632595 | |||||||
chr2:163632600 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20794G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632600 | |||||||
chr2:163632601 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20795T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632601 | |||||||
chr2:163632602 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20796A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632602 | |||||||
chr2:163632605 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20799T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632605 | |||||||
chr2:163632606 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20800T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632606 | |||||||
chr2:163632607 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20801A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632607 | |||||||
chr2:163632609 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20803A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632609 | |||||||
chr2:163632614 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20808T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632614 | |||||||
chr2:163632615 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20809A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632615 | |||||||
chr2:163632616 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20810T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632616 | |||||||
chr2:163632617 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20811T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632617 | |||||||
chr2:163632618 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20812T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632618 | |||||||
chr2:163632619 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20813T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632619 | |||||||
chr2:163632620 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20814T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632620 | |||||||
chr2:163632636 | T | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(134): Show |
137 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.26-20830A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632636 | |||||||
chr2:163632636 | T | C | 1 | a0001c0001t0060g0059 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-20830A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632636 | |||||||
chr2:163632637 | T | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(135): Show |
138 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.26-20831A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632637 | |||||||
chr2:163632676 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20870G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632676 | |||||||
chr2:163632690 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20884A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632690 | |||||||
chr2:163632704 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-20898A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632704 | |||||||
chr2:163632774 | C | T | 9 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0015g0123 others(6): Show |
9 | HG00558.hp1 HG02280.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-20968G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632774 | |||||||
chr2:163632958 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(30): Show |
34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-21152T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163632958 | |||||||
chr2:163633051 | G | C | 5 | a0001c0001t0003g0102 a0001c0001t0009g0128 a0001c0002t0003g0100 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-21245C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633051 | |||||||
chr2:163633427 | T | C | 1 | a0001c0001t0043g0210 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.26-21621A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633427 | |||||||
chr2:163633487 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21681A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633487 | |||||||
chr2:163633491 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21685A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633491 | |||||||
chr2:163633495 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21689G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633495 | |||||||
chr2:163633498 | G | C | 1 | a0001c0001t0023g0166 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.26-21692C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633498 | |||||||
chr2:163633514 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21708G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633514 | |||||||
chr2:163633517 | CCTCCACA others(17): Show |
C | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21735_26-21712d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633517 | |||||||
chr2:163633549 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21743G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633549 | |||||||
chr2:163633556 | A | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(135): Show |
138 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.26-21750T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633556 | |||||||
chr2:163633565 | T | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21759A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633565 | |||||||
chr2:163633570 | T | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21764A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633570 | |||||||
chr2:163633574 | A | T | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21768T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633574 | |||||||
chr2:163633576 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21770G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633576 | |||||||
chr2:163633586 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21780G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633586 | |||||||
chr2:163633587 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21781G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633587 | |||||||
chr2:163633592 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21786G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633592 | |||||||
chr2:163633603 | G | T | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-21797C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633603 | |||||||
chr2:163633613 | A | T | 1 | a0001c0001t0002g0146 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.26-21807T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633613 | |||||||
chr2:163633624 | G | A | 3 | a0001c0001t0004g0192 a0001c0001t0007g0020 a0001c0002t0011g0092 |
3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-21818C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633624 | |||||||
chr2:163633731 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(42): Show |
46 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.26-21925G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163633731 | |||||||
chr2:163634019 | A | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
199 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.26-22213T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634019 | |||||||
chr2:163634086 | A | ATGCG | 6 | a0001c0001t0017g0147 a0001c0001t0017g0148 a0001c0001t0017g0151 others(3): Show |
6 | NA18959.hp2 NA18961.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-22284_26-22281d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634086 | |||||||
chr2:163634089 | C | CGT | 25 | a0001c0001t0001g0043 a0001c0001t0001g0118 a0001c0001t0001g0137 others(22): Show |
25 | HG00408.hp1 HG00423.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-22285_26-22284d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | |||||||
chr2:163634089 | C | CGTGT | 105 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0018 others(102): Show |
105 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.26-22287_26-22284d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | |||||||
chr2:163634089 | C | CGTGTGT | 17 | a0001c0001t0001g0079 a0001c0001t0001g0111 a0001c0001t0001g0164 others(14): Show |
17 | HG00408.hp2 HG01261.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-22289_26-22284d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | |||||||
chr2:163634089 | C | CGTGTGTG others(3): Show |
3 | a0001c0001t0001g0002 a0001c0001t0002g0229 a0001c0001t0063g0234 |
3 | HG01175.hp2 NA18985.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-22293_26-22284d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | |||||||
chr2:163634089 | CGT | C | 11 | a0001c0001t0005g0117 a0001c0001t0007g0020 a0001c0001t0008g0168 others(8): Show |
11 | HG00558.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-22285_26-22284d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | |||||||
chr2:163634089 | CGTGT | C | 6 | a0001c0001t0004g0192 a0001c0001t0015g0123 a0001c0001t0015g0124 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-22287_26-22284d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634089 | |||||||
chr2:163634114 | G | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(29): Show |
33 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-22308C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634114 | |||||||
chr2:163634413 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-22607A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634413 | |||||||
chr2:163634723 | C | T | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-22917G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634723 | |||||||
chr2:163634794 | T | C | 3 | a0001c0001t0002g0229 a0001c0001t0052g0218 a0001c0001t0064g0238 |
3 | HG00408.hp2 HG02129.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-22988A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634794 | |||||||
chr2:163634958 | G | T | 1 | a0001c0001t0003g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-23152C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163634958 | |||||||
chr2:163635106 | A | G | 5 | a0001c0001t0003g0102 a0001c0001t0009g0128 a0001c0002t0003g0100 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-23300T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635106 | |||||||
chr2:163635175 | G | A | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-23369C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635175 | |||||||
chr2:163635532 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.26-23726G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635532 | |||||||
chr2:163635681 | T | C | 1 | a0001c0001t0082g0258 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-23875A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635681 | |||||||
chr2:163635884 | C | G | 5 | a0001c0001t0003g0102 a0001c0001t0009g0128 a0001c0002t0003g0100 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-24078G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635884 | |||||||
chr2:163635967 | A | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-24161T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163635967 | |||||||
chr2:163636088 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-24282T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636088 | |||||||
chr2:163636426 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.26-24620G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636426 | |||||||
chr2:163636594 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.26-24788T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636594 | |||||||
chr2:163636653 | T | C | 1 | a0003c0006t0009g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.26-24847A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636653 | |||||||
chr2:163636733 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.26-24927A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636733 | |||||||
chr2:163636944 | T | C | 1 | a0001c0001t0012g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.26-25138A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636944 | |||||||
chr2:163636951 | C | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0141 others(16): Show |
19 | HG00423.hp1 HG02027.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-25145G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636951 | |||||||
chr2:163636976 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0010g0061 |
2 | NA18985.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.26-25170C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636976 | |||||||
chr2:163636977 | G | A | 2 | a0001c0001t0004g0190 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-25171C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636977 | |||||||
chr2:163636987 | G | A | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-25181C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163636987 | |||||||
chr2:163637097 | C | T | 4 | a0001c0001t0015g0123 a0001c0001t0015g0124 a0001c0001t0021g0184 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-25291G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637097 | |||||||
chr2:163637222 | C | T | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-25416G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637222 | |||||||
chr2:163637328 | G | C | 2 | a0001c0001t0003g0183 a0001c0001t0011g0173 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.26-25522C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637328 | |||||||
chr2:163637520 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.26-25714T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637520 | |||||||
chr2:163637533 | T | C | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.26-25727A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637533 | |||||||
chr2:163637667 | C | CT | 8 | a0001c0001t0001g0219 a0001c0001t0002g0074 a0001c0001t0003g0187 others(5): Show |
8 | HG01175.hp1 HG02040.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-25862dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637667 | |||||||
chr2:163637667 | CT | C | 12 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0015g0123 others(9): Show |
12 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-25862delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637667 | |||||||
chr2:163637721 | C | T | 4 | a0001c0001t0015g0123 a0001c0001t0015g0124 a0001c0001t0021g0184 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-25915G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637721 | |||||||
chr2:163637776 | A | G | 1 | a0001c0002t0028g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.26-25970T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637776 | |||||||
chr2:163637930 | TG | T | 5 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0014g0015 others(2): Show |
5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-26125delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163637930 | |||||||
chr2:163638012 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-26206G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638012 | |||||||
chr2:163638215 | G | A | 1 | a0001c0001t0081g0257 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26-26409C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638215 | |||||||
chr2:163638262 | A | T | 4 | a0001c0001t0015g0123 a0001c0001t0015g0124 a0001c0001t0021g0184 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-26456T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638262 | |||||||
chr2:163638713 | G | C | 5 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0014g0015 others(2): Show |
5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-26907C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638713 | |||||||
chr2:163638748 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-26942G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638748 | |||||||
chr2:163638917 | AC | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0066 a0001c0001t0006g0062 others(3): Show |
6 | HG00735.hp1 HG01167.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-27112delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638917 | |||||||
chr2:163638942 | A | C | 3 | a0001c0001t0001g0053 a0001c0001t0008g0072 a0001c0001t0009g0197 |
3 | NA18747.hp2 NA18941.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.26-27136T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163638942 | |||||||
chr2:163639125 | T | C | 1 | a0001c0001t0020g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.26-27319A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639125 | |||||||
chr2:163639150 | C | A | 7 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0021g0243 others(4): Show |
7 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-27344G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639150 | |||||||
chr2:163639320 | G | T | 3 | a0001c0001t0002g0229 a0001c0001t0052g0218 a0001c0001t0064g0238 |
3 | HG00408.hp2 HG02129.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-27514C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639320 | |||||||
chr2:163639436 | T | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(28): Show |
32 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-27630A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639436 | |||||||
chr2:163639490 | A | T | 1 | a0001c0001t0003g0193 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-27684T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639490 | |||||||
chr2:163639511 | T | C | 2 | a0001c0001t0050g0172 a0001c0001t0057g0108 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-27705A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639511 | |||||||
chr2:163639558 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.26-27752C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639558 | |||||||
chr2:163639802 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0098 |
2 | HG02818.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.26-27996A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639802 | |||||||
chr2:163639825 | T | G | 1 | a0001c0001t0022g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.26-28019A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639825 | |||||||
chr2:163639857 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
144 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.26-28051A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163639857 | |||||||
chr2:163640169 | T | C | 3 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0060g0059 |
3 | HG02040.hp1 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-28363A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163640169 | |||||||
chr2:163640291 | G | T | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-28485C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163640291 | |||||||
chr2:163641078 | C | T | 9 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0015g0126 others(6): Show |
9 | HG00558.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-29272G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641078 | |||||||
chr2:163641098 | G | A | 1 | a0001c0001t0002g0198 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.26-29292C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641098 | |||||||
chr2:163641110 | A | T | 20 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0152 others(17): Show |
20 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.26-29304T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641110 | |||||||
chr2:163641139 | A | G | 3 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0060g0059 |
3 | HG02040.hp1 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-29333T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641139 | |||||||
chr2:163641167 | G | A | 4 | a0001c0001t0015g0123 a0001c0001t0015g0124 a0001c0001t0021g0184 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-29361C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641167 | |||||||
chr2:163641281 | G | A | 1 | a0001c0001t0012g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.26-29475C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641281 | |||||||
chr2:163641388 | AG | A | 7 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0021g0243 others(4): Show |
7 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-29583delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641388 | |||||||
chr2:163641436 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(189): Show |
193 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.26-29630G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641436 | |||||||
chr2:163641525 | C | T | 11 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0015g0123 others(8): Show |
11 | HG00558.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-29719G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641525 | |||||||
chr2:163641663 | G | A | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-29857C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641663 | |||||||
chr2:163641739 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26-29933T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641739 | |||||||
chr2:163641809 | T | C | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-30003A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641809 | |||||||
chr2:163641873 | A | G | 1 | a0001c0001t0012g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.26-30067T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641873 | |||||||
chr2:163641918 | C | A | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-30112G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163641918 | |||||||
chr2:163642394 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0011g0114 a0001c0001t0011g0189 others(1): Show |
4 | HG00735.hp2 HG02723.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-30588A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642394 | |||||||
chr2:163642417 | G | C | 1 | a0001c0001t0015g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.26-30611C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642417 | |||||||
chr2:163642534 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0011g0114 a0001c0001t0011g0189 others(1): Show |
4 | HG00735.hp2 HG02723.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-30728A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642534 | |||||||
chr2:163642576 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.26-30770A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642576 | |||||||
chr2:163642793 | T | A | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-30987A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163642793 | |||||||
chr2:163643005 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
199 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.26-31199T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643005 | |||||||
chr2:163643273 | G | A | 1 | a0001c0001t0007g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.26-31467C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643273 | |||||||
chr2:163643414 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.26-31608C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643414 | |||||||
chr2:163643549 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.26-31743C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643549 | |||||||
chr2:163643644 | C | T | 1 | a0001c0001t0004g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-31838G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643644 | |||||||
chr2:163643650 | C | CA | 26 | a0001c0001t0001g0118 a0001c0001t0001g0219 a0001c0001t0002g0213 others(23): Show |
26 | HG00323.hp1 HG00735.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-31845dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643650 | |||||||
chr2:163643650 | CA | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0041 others(24): Show |
27 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.26-31845delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643650 | |||||||
chr2:163643691 | T | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(252): Show |
256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.26-31885A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643691 | |||||||
chr2:163643733 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.26-31927G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643733 | |||||||
chr2:163643765 | C | A | 7 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0021g0243 others(4): Show |
7 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-31959G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643765 | |||||||
chr2:163643904 | G | T | 3 | a0001c0001t0004g0192 a0001c0001t0007g0020 a0001c0002t0011g0092 |
3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-32098C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643904 | |||||||
chr2:163643905 | C | A | 3 | a0001c0001t0004g0192 a0001c0001t0007g0020 a0001c0002t0011g0092 |
3 | HG02055.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-32099G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643905 | |||||||
chr2:163643919 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.26-32113G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643919 | |||||||
chr2:163643932 | C | CA | 16 | a0001c0001t0001g0110 a0001c0001t0001g0220 a0001c0001t0003g0087 others(13): Show |
16 | HG01433.hp2 HG02109.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-32127dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAA | 6 | a0001c0001t0004g0190 a0001c0001t0013g0101 a0001c0001t0021g0243 others(3): Show |
6 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-32129_26-32127d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAA | 7 | a0001c0001t0001g0066 a0001c0001t0001g0139 a0001c0001t0001g0221 others(4): Show |
7 | HG00735.hp1 HG02293.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-32132_26-32127d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0098 a0001c0001t0001g0152 a0001c0001t0002g0050 others(10): Show |
13 | HG01070.hp2 HG01261.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-32135_26-32127d others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(3): Show |
42 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0021 others(39): Show |
42 | HG00140.hp2 HG00609.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.26-32136_26-32127d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(4): Show |
46 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0055 others(43): Show |
46 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.26-32137_26-32127d others(13): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(5): Show |
17 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0028 others(14): Show |
17 | HG00741.hp1 HG01106.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-32138_26-32127d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(6): Show |
10 | a0001c0001t0001g0082 a0001c0001t0002g0213 a0001c0001t0003g0106 others(7): Show |
10 | HG01106.hp2 HG01891.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-32139_26-32127d others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0002g0019 a0001c0001t0026g0095 |
2 | HG02451.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.26-32140_26-32127d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.26-32143_26-32127d others(19): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-32144_26-32127d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | CA | C | 15 | a0001c0001t0001g0137 a0001c0001t0001g0219 a0001c0001t0002g0146 others(12): Show |
15 | HG00323.hp1 HG00558.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-32127delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643932 | CAAAAAAA | C | 15 | a0001c0001t0001g0141 a0001c0001t0001g0196 a0001c0001t0001g0199 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.26-32133_26-32127d others(9): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643932 | |||||||
chr2:163643957 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0006g0006 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.26-32152_26-32151i others(13): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163643957 | |||||||
chr2:163644008 | C | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(195): Show |
199 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.26-32202G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644008 | |||||||
chr2:163644099 | G | T | 1 | a0001c0001t0057g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-32293C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644099 | |||||||
chr2:163644382 | T | C | 9 | a0001c0001t0001g0141 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
9 | HG02155.hp1 NA18612.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-32576A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644382 | |||||||
chr2:163644706 | A | T | 5 | a0001c0001t0003g0102 a0001c0001t0009g0128 a0001c0002t0003g0100 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-32900T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644706 | |||||||
chr2:163644796 | T | G | 1 | a0001c0001t0007g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.26-32990A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163644796 | |||||||
chr2:163645124 | A | G | 11 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0015g0123 others(8): Show |
11 | HG00558.hp1 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-33318T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645124 | |||||||
chr2:163645152 | T | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(30): Show |
34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-33346A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645152 | |||||||
chr2:163645161 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(30): Show |
34 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-33355T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645161 | |||||||
chr2:163645245 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(190): Show |
194 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.26-33439T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645245 | |||||||
chr2:163645263 | C | A | 2 | a0001c0001t0050g0172 a0001c0001t0057g0108 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-33457G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645263 | |||||||
chr2:163645263 | C | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
134 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.26-33457G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645263 | |||||||
chr2:163645510 | T | C | 5 | a0001c0001t0013g0101 a0001c0001t0021g0243 a0001c0001t0025g0109 others(2): Show |
5 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-33704A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645510 | |||||||
chr2:163645574 | G | A | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-33768C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645574 | |||||||
chr2:163645991 | G | C | 1 | a0001c0001t0003g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.26-34185C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163645991 | |||||||
chr2:163646180 | C | T | 3 | a0001c0001t0005g0033 a0001c0001t0035g0246 a0001c0008t0035g0248 |
3 | HG00408.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-34374G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646180 | |||||||
chr2:163646312 | A | T | 1 | a0001c0001t0029g0215 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.26-34506T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646312 | |||||||
chr2:163646330 | C | G | 7 | a0001c0001t0001g0219 a0001c0001t0003g0187 a0001c0001t0004g0133 others(4): Show |
7 | HG01175.hp1 HG02040.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-34524G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646330 | |||||||
chr2:163646777 | A | G | 2 | a0001c0001t0031g0091 a0001c0001t0059g0093 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26-34971T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646777 | |||||||
chr2:163646949 | C | T | 2 | a0001c0001t0050g0172 a0001c0001t0057g0108 |
2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.26-35143G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163646949 | |||||||
chr2:163647046 | G | C | 122 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(119): Show |
123 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.26-35240C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647046 | |||||||
chr2:163647107 | G | A | 1 | a0001c0001t0002g0004 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.26-35301C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647107 | |||||||
chr2:163647191 | G | A | 56 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0112 others(53): Show |
56 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.26-35385C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647191 | |||||||
chr2:163647279 | A | C | 5 | a0001c0001t0002g0019 a0001c0001t0005g0033 a0001c0001t0014g0015 others(2): Show |
5 | HG00408.hp1 HG03688.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-35473T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647279 | |||||||
chr2:163647368 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0003g0187 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-35562G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647368 | |||||||
chr2:163647411 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-35605A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647411 | |||||||
chr2:163647627 | G | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(31): Show |
35 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.26-35821C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647627 | |||||||
chr2:163647678 | A | C | 61 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0112 others(58): Show |
61 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.26-35872T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647678 | |||||||
chr2:163647792 | T | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(31): Show |
35 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.26-35986A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647792 | |||||||
chr2:163647810 | A | G | 40 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(37): Show |
41 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.26-36004T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647810 | |||||||
chr2:163647852 | A | G | 4 | a0001c0001t0029g0022 a0001c0001t0037g0259 a0001c0001t0051g0084 others(1): Show |
4 | NA18960.hp1 NA18995.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-36046T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163647852 | |||||||
chr2:163648026 | C | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0082 others(3): Show |
6 | HG00741.hp1 HG01106.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-36220G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648026 | |||||||
chr2:163648073 | T | G | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-36267A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648073 | |||||||
chr2:163648129 | C | A | 3 | a0001c0001t0003g0106 a0001c0001t0026g0094 a0001c0001t0026g0095 |
3 | HG02451.hp1 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-36323G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648129 | |||||||
chr2:163648213 | C | A | 17 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0002g0146 others(14): Show |
17 | HG00323.hp1 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-36407G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648213 | |||||||
chr2:163648450 | C | G | 1 | a0001c0001t0006g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.26-36644G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648450 | |||||||
chr2:163648793 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(215): Show |
219 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.26-36987A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648793 | |||||||
chr2:163648897 | A | G | 2 | a0001c0001t0035g0246 a0001c0008t0035g0248 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-37091T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648897 | |||||||
chr2:163648967 | A | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(182): Show |
186 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.26-37161T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648967 | |||||||
chr2:163648974 | A | T | 11 | a0001c0001t0001g0118 a0001c0001t0001g0219 a0001c0001t0004g0190 others(8): Show |
11 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-37168T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163648974 | |||||||
chr2:163649133 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(153): Show |
157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.26-37327T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649133 | |||||||
chr2:163649225 | G | A | 3 | a0001c0001t0006g0099 a0001c0001t0070g0103 a0001c0002t0007g0104 |
3 | HG02055.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-37419C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649225 | |||||||
chr2:163649255 | G | A | 5 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0023g0157 others(2): Show |
5 | HG00558.hp1 HG01496.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-37449C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649255 | |||||||
chr2:163649300 | A | G | 1 | a0001c0001t0043g0210 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.26-37494T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649300 | |||||||
chr2:163649428 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.26-37622A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649428 | |||||||
chr2:163649568 | G | A | 1 | a0001c0001t0057g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-37762C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649568 | |||||||
chr2:163649649 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.26-37843A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649649 | |||||||
chr2:163649675 | A | T | 1 | a0001c0001t0019g0254 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.26-37869T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649675 | |||||||
chr2:163649968 | G | A | 9 | a0001c0001t0001g0118 a0001c0001t0001g0219 a0001c0001t0011g0114 others(6): Show |
9 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-38162C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163649968 | |||||||
chr2:163650086 | A | G | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-38280T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650086 | |||||||
chr2:163650169 | T | G | 25 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0004g0133 others(22): Show |
25 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-38363A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650169 | |||||||
chr2:163650211 | C | T | 2 | a0001c0001t0070g0103 a0001c0002t0007g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-38405G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650211 | |||||||
chr2:163650330 | A | T | 9 | a0001c0001t0001g0118 a0001c0001t0001g0219 a0001c0001t0011g0114 others(6): Show |
9 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-38524T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650330 | |||||||
chr2:163650363 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.26-38557A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650363 | |||||||
chr2:163650431 | T | C | 26 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0139 others(23): Show |
27 | HG01261.hp1 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-38625A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650431 | |||||||
chr2:163650467 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(182): Show |
186 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.26-38661T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650467 | |||||||
chr2:163650880 | A | G | 23 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0139 others(20): Show |
24 | HG01261.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.26-39074T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650880 | |||||||
chr2:163650927 | C | A | 1 | a0001c0001t0003g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26-39121G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650927 | |||||||
chr2:163650984 | C | A | 3 | a0001c0001t0003g0106 a0001c0001t0026g0094 a0001c0001t0026g0095 |
3 | HG02451.hp1 HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-39178G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163650984 | |||||||
chr2:163651054 | A | AGAT | 4 | a0001c0001t0001g0041 a0001c0001t0002g0005 a0001c0001t0032g0014 others(1): Show |
4 | NA18969.hp2 NA19065.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-39251_26-39249d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651054 | |||||||
chr2:163651064 | A | G | 10 | a0001c0001t0001g0118 a0001c0001t0001g0152 a0001c0001t0001g0219 others(7): Show |
10 | HG00735.hp2 HG01515.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-39258T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651064 | |||||||
chr2:163651286 | C | A | 1 | a0001c0001t0018g0206 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.26-39480G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651286 | |||||||
chr2:163651385 | C | T | 1 | a0001c0001t0030g0127 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.26-39579G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651385 | |||||||
chr2:163651405 | G | A | 3 | a0001c0001t0003g0187 a0001c0001t0015g0126 a0001c0002t0016g0067 |
3 | HG02257.hp1 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.26-39599C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651405 | |||||||
chr2:163651724 | T | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(258): Show |
262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.26-39918A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163651724 | |||||||
chr2:163652343 | A | AAC | 38 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(35): Show |
38 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.26-40539_26-40538d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | |||||||
chr2:163652343 | A | AACAC | 27 | a0001c0001t0001g0043 a0001c0001t0001g0111 a0001c0001t0001g0118 others(24): Show |
28 | HG00408.hp2 HG01361.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.26-40541_26-40538d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | |||||||
chr2:163652343 | A | AACACAC | 4 | a0001c0001t0005g0153 a0001c0001t0005g0160 a0001c0001t0016g0130 others(1): Show |
4 | HG01261.hp1 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-40543_26-40538d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | |||||||
chr2:163652343 | A | AACACACA others(1): Show |
2 | a0001c0001t0001g0219 a0001c0001t0003g0097 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.26-40545_26-40538d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652343 | |||||||
chr2:163652345 | CACACACA others(9): Show |
C | 1 | a0001c0001t0006g0239 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.26-40555_26-40540d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652345 | |||||||
chr2:163652355 | CACACAA | C | 3 | a0001c0001t0005g0033 a0001c0001t0015g0123 a0001c0001t0015g0124 |
3 | HG00408.hp1 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-40555_26-40550d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652355 | |||||||
chr2:163652357 | CACAA | C | 12 | a0001c0001t0001g0112 a0001c0001t0002g0064 a0001c0001t0003g0106 others(9): Show |
12 | HG00423.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-40555_26-40552d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652357 | |||||||
chr2:163652359 | CAA | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0002g0035 others(9): Show |
12 | HG01071.hp2 HG02155.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-40555_26-40554d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652359 | |||||||
chr2:163652361 | A | AAC | 7 | a0001c0001t0001g0220 a0001c0001t0013g0194 a0001c0001t0020g0263 others(4): Show |
7 | HG01496.hp1 HG01496.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-40557_26-40556d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | |||||||
chr2:163652361 | A | AACAC | 65 | a0001c0001t0001g0016 a0001c0001t0001g0137 a0001c0001t0001g0140 others(62): Show |
65 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.26-40559_26-40556d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | |||||||
chr2:163652361 | A | AACACAC | 11 | a0001c0001t0001g0055 a0001c0001t0003g0183 a0001c0001t0007g0182 others(8): Show |
11 | HG00558.hp1 HG01515.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-40561_26-40556d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | |||||||
chr2:163652361 | A | AACACACA others(1): Show |
6 | a0001c0001t0001g0119 a0001c0001t0006g0099 a0001c0001t0014g0025 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-40563_26-40556d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | |||||||
chr2:163652361 | A | AACACACA others(3): Show |
1 | a0001c0001t0004g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.26-40565_26-40556d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | |||||||
chr2:163652361 | A | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(129): Show |
133 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.26-40555T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652361 | |||||||
chr2:163652481 | C | CA | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.26-40676dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652481 | |||||||
chr2:163652634 | T | C | 1 | a0001c0001t0075g0009 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.26-40828A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652634 | |||||||
chr2:163652744 | A | T | 15 | a0001c0001t0001g0055 a0001c0001t0001g0119 a0001c0001t0001g0176 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-40938T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652744 | |||||||
chr2:163652796 | A | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-40990T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652796 | |||||||
chr2:163652914 | T | C | 1 | a0001c0001t0003g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.26-41108A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652914 | |||||||
chr2:163652918 | G | A | 3 | a0001c0001t0014g0015 a0001c0001t0035g0246 a0001c0008t0035g0248 |
3 | HG03688.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-41112C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163652918 | |||||||
chr2:163653129 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0014g0025 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.26-41323A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653129 | |||||||
chr2:163653386 | T | C | 4 | a0001c0001t0003g0183 a0001c0001t0006g0099 a0001c0001t0007g0182 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-41580A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653386 | |||||||
chr2:163653501 | T | C | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-41695A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653501 | |||||||
chr2:163653749 | G | C | 5 | a0001c0001t0003g0183 a0001c0001t0006g0099 a0001c0001t0007g0182 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-41943C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653749 | |||||||
chr2:163653823 | T | A | 1 | a0001c0001t0015g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.26-42017A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653823 | |||||||
chr2:163653995 | G | A | 3 | a0001c0001t0014g0015 a0001c0001t0035g0246 a0001c0008t0035g0248 |
3 | HG03688.hp1 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-42189C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163653995 | |||||||
chr2:163654005 | A | C | 1 | a0001c0001t0057g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-42199T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654005 | |||||||
chr2:163654128 | T | C | 1 | a0001c0001t0027g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.26-42322A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654128 | |||||||
chr2:163654214 | C | A | 1 | a0001c0001t0021g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.26-42408G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654214 | |||||||
chr2:163654419 | T | C | 22 | a0001c0001t0001g0139 a0001c0001t0003g0097 a0001c0001t0003g0102 others(19): Show |
22 | HG01175.hp1 HG01261.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.26-42613A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654419 | |||||||
chr2:163654605 | T | C | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.26-42799A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654605 | |||||||
chr2:163654778 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.26-42972A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654778 | |||||||
chr2:163654841 | C | T | 3 | a0001c0001t0004g0133 a0001c0001t0027g0107 a0001c0001t0050g0172 |
3 | HG02559.hp2 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.26-43035G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654841 | |||||||
chr2:163654911 | AAGG | A | 7 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 others(4): Show |
7 | HG02280.hp2 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-43108_26-43106d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163654911 | |||||||
chr2:163655039 | G | A | 1 | a0001c0001t0077g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.26-43233C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655039 | |||||||
chr2:163655111 | T | TAAGAAAT others(237): Show |
1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-43306_26-43305i others(246): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655111 | |||||||
chr2:163655260 | C | T | 3 | a0001c0001t0003g0193 a0001c0001t0015g0123 a0001c0001t0015g0124 |
3 | HG02809.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-43454G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655260 | |||||||
chr2:163655292 | T | C | 1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-43486A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655292 | |||||||
chr2:163655344 | G | C | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.26-43538C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655344 | |||||||
chr2:163655369 | C | T | 2 | a0001c0001t0023g0166 a0001c0001t0067g0195 |
2 | HG01515.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.26-43563G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655369 | |||||||
chr2:163655437 | T | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0150 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.26-43631A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655437 | |||||||
chr2:163655550 | T | A | 1 | a0001c0001t0001g0236 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.26-43744A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655550 | |||||||
chr2:163655597 | G | T | 1 | a0001c0003t0002g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.26-43791C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655597 | |||||||
chr2:163655731 | A | G | 7 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 others(4): Show |
7 | HG02280.hp2 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-43925T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655731 | |||||||
chr2:163655785 | G | GCA | 34 | a0001c0001t0001g0078 a0001c0001t0001g0199 a0001c0001t0001g0200 others(31): Show |
34 | HG00408.hp2 HG00609.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-43981_26-43980d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655785 | |||||||
chr2:163655785 | G | GCACA | 17 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0196 others(14): Show |
17 | HG00423.hp1 HG02027.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-43983_26-43980d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655785 | |||||||
chr2:163655804 | C | CACACAGA others(1): Show |
6 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0001t0021g0243 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-43999_26-43998i others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | CACAG | 4 | a0001c0001t0003g0106 a0001c0001t0025g0109 a0001c0001t0031g0131 others(1): Show |
4 | HG02280.hp2 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-43999_26-43998i others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | CACAGAG | 17 | a0001c0001t0001g0139 a0001c0001t0003g0097 a0001c0001t0003g0102 others(14): Show |
17 | HG01175.hp1 HG01261.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-43999_26-43998i others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | CACAGAGA others(1): Show |
3 | a0001c0001t0003g0193 a0001c0001t0015g0123 a0001c0001t0015g0124 |
3 | HG02809.hp2 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-43999_26-43998i others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | CACAGAGA others(3): Show |
3 | a0001c0001t0001g0118 a0001c0001t0004g0190 a0001c0002t0013g0191 |
3 | HG03098.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.26-43999_26-43998i others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | CAG | 3 | a0001c0001t0006g0029 a0001c0001t0045g0177 a0001c0001t0057g0108 |
3 | HG01884.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.26-44000_26-43999d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | CAGAG | 11 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-44002_26-43999d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | CAGAGAG | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-44004_26-43999d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655804 | C | G | 2 | a0001c0001t0029g0022 a0001c0001t0051g0084 |
2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-43998G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655804 | |||||||
chr2:163655806 | G | C | 4 | a0001c0001t0001g0140 a0001c0001t0002g0203 a0001c0001t0012g0024 others(1): Show |
4 | HG03491.hp1 HG03831.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-44000C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655806 | |||||||
chr2:163655810 | G | C | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-44004C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655810 | |||||||
chr2:163655937 | G | A | 2 | a0001c0001t0029g0022 a0001c0001t0051g0084 |
2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-44131C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163655937 | |||||||
chr2:163656049 | T | C | 1 | a0001c0001t0006g0023 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.26-44243A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656049 | |||||||
chr2:163656108 | C | A | 72 | a0001c0001t0001g0016 a0001c0001t0001g0111 a0001c0001t0001g0112 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.26-44302G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656108 | |||||||
chr2:163656185 | G | T | 2 | a0001c0001t0008g0168 a0001c0001t0008g0181 |
2 | HG00558.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.26-44379C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656185 | |||||||
chr2:163656241 | C | T | 31 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0139 others(28): Show |
31 | HG00735.hp2 HG01175.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.26-44435G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656241 | |||||||
chr2:163656330 | T | C | 1 | a0001c0001t0038g0032 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.26-44524A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656330 | |||||||
chr2:163656354 | A | G | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-44548T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656354 | |||||||
chr2:163656360 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.26-44554C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656360 | |||||||
chr2:163656372 | G | A | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-44566C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656372 | |||||||
chr2:163656623 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.26-44817C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656623 | |||||||
chr2:163656685 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.26-44879C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656685 | |||||||
chr2:163656799 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.26-44993A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163656799 | |||||||
chr2:163657091 | G | A | 2 | a0001c0001t0004g0190 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-45285C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657091 | |||||||
chr2:163657104 | C | A | 2 | a0001c0001t0035g0246 a0001c0008t0035g0248 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-45298G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657104 | |||||||
chr2:163657115 | G | GA | 63 | a0001c0001t0001g0040 a0001c0001t0001g0056 a0001c0001t0001g0110 others(60): Show |
63 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.26-45310dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657115 | |||||||
chr2:163657115 | G | GAA | 5 | a0001c0001t0001g0043 a0001c0001t0002g0223 a0001c0001t0003g0183 others(2): Show |
5 | HG02027.hp1 HG02027.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-45311_26-45310d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657115 | |||||||
chr2:163657115 | GA | G | 5 | a0001c0001t0006g0076 a0001c0001t0024g0001 a0001c0001t0035g0246 others(2): Show |
6 | HG01978.hp2 HG02970.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-45310delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657115 | |||||||
chr2:163657500 | C | CTG | 9 | a0001c0001t0001g0082 a0001c0001t0001g0141 a0001c0001t0006g0099 others(6): Show |
9 | HG00323.hp2 HG01106.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-45696_26-45695d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657500 | C | CTGTG | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(91): Show |
94 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.26-45698_26-45695d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657500 | C | CTGTGTG | 41 | a0001c0001t0001g0007 a0001c0001t0001g0115 a0001c0001t0001g0176 others(38): Show |
42 | HG00408.hp2 HG00609.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.26-45700_26-45695d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657500 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0118 a0001c0001t0001g0202 a0001c0001t0002g0050 others(4): Show |
7 | HG02015.hp1 HG02027.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-45702_26-45695d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657500 | C | CTGTGTGT others(3): Show |
17 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(14): Show |
17 | HG00423.hp1 HG02027.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-45704_26-45695d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657500 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0002g0208 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.26-45706_26-45695d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657500 | CTG | C | 26 | a0001c0001t0001g0139 a0001c0001t0003g0102 a0001c0001t0003g0240 others(23): Show |
26 | HG00558.hp1 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.26-45696_26-45695d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657500 | CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 others(2): Show |
5 | HG02280.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-45704_26-45695d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657500 | |||||||
chr2:163657551 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.26-45745A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657551 | |||||||
chr2:163657627 | A | C | 3 | a0001c0002t0007g0135 a0001c0002t0007g0136 a0001c0002t0028g0134 |
3 | HG03225.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26-45821T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657627 | |||||||
chr2:163657729 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(193): Show |
197 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.26-45923A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657729 | |||||||
chr2:163657746 | A | G | 1 | a0001c0001t0052g0218 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.26-45940T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657746 | |||||||
chr2:163657821 | T | C | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-46015A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657821 | |||||||
chr2:163657930 | T | C | 5 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(2): Show |
5 | HG00735.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-46124A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163657930 | |||||||
chr2:163658087 | C | G | 1 | a0001c0001t0015g0124 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.26-46281G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658087 | |||||||
chr2:163658123 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.26-46317G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658123 | |||||||
chr2:163658364 | G | GCT | 9 | a0001c0001t0001g0140 a0001c0001t0005g0153 a0001c0001t0006g0239 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-46560_26-46559d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | G | GCTCT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0139 a0001c0001t0012g0122 others(2): Show |
5 | HG01261.hp1 HG02451.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-46562_26-46559d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | G | GCTCTCT | 8 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0005g0160 others(5): Show |
8 | HG01175.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-46564_26-46559d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | G | GCTCTCTC others(1): Show |
5 | a0001c0001t0003g0240 a0001c0001t0023g0157 a0001c0001t0071g0241 others(2): Show |
5 | HG01496.hp2 HG01891.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-46566_26-46559d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | G | GCTCTCTC others(5): Show |
1 | a0001c0001t0058g0155 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.26-46570_26-46559d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | G | GCTCTCTC others(7): Show |
1 | a0001c0001t0005g0159 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.26-46572_26-46559d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | G | GCTCTCTC others(9): Show |
1 | a0001c0001t0031g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26-46574_26-46559d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCT | G | 21 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0141 others(18): Show |
21 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.26-46560_26-46559d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCT | G | 20 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0019g0254 others(17): Show |
20 | HG00741.hp2 HG01070.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.26-46562_26-46559d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCT | G | 13 | a0001c0001t0001g0143 a0001c0001t0001g0158 a0001c0001t0001g0220 others(10): Show |
13 | HG00558.hp2 HG01433.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-46564_26-46559d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCTC others(3): Show |
G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0056 |
2 | HG01255.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.26-46568_26-46559d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCTC others(5): Show |
G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(77): Show |
80 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.26-46570_26-46559d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCTC others(7): Show |
G | 10 | a0001c0001t0001g0055 a0001c0001t0001g0119 a0001c0001t0003g0105 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-46572_26-46559d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCTC others(9): Show |
G | 12 | a0001c0001t0001g0176 a0001c0001t0002g0075 a0001c0001t0003g0183 others(9): Show |
13 | HG01106.hp1 HG02258.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-46574_26-46559d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCTC others(11): Show |
G | 4 | a0001c0001t0001g0118 a0001c0001t0003g0106 a0001c0001t0031g0131 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-46576_26-46559d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCTC others(13): Show |
G | 9 | a0001c0001t0003g0116 a0001c0001t0004g0133 a0001c0001t0004g0190 others(6): Show |
9 | HG02451.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-46578_26-46559d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658364 | GCTCTCTC others(15): Show |
G | 47 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(44): Show |
47 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-46580_26-46559d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658364 | |||||||
chr2:163658380 | T | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0181 |
2 | HG00558.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.26-46574A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658380 | |||||||
chr2:163658400 | T | G | 2 | a0001c0001t0004g0190 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-46594A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658400 | |||||||
chr2:163658410 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0018g0206 |
2 | NA18612.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.26-46604C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658410 | |||||||
chr2:163658425 | G | C | 1 | a0001c0001t0001g0007 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.26-46619C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658425 | |||||||
chr2:163658518 | T | C | 1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-46712A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658518 | |||||||
chr2:163658524 | C | T | 26 | a0001c0001t0001g0139 a0001c0001t0003g0097 a0001c0001t0003g0102 others(23): Show |
26 | HG00558.hp1 HG01175.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-46718G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658524 | |||||||
chr2:163658678 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.26-46872C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658678 | |||||||
chr2:163658730 | C | G | 23 | a0001c0001t0001g0139 a0001c0001t0003g0097 a0001c0001t0003g0102 others(20): Show |
23 | HG00558.hp1 HG01175.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.26-46924G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658730 | |||||||
chr2:163658970 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0018g0027 |
2 | NA18941.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.26-47164C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163658970 | |||||||
chr2:163659027 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.26-47221C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659027 | |||||||
chr2:163659054 | C | T | 32 | a0001c0001t0001g0115 a0001c0001t0001g0139 a0001c0001t0003g0097 others(29): Show |
32 | HG00558.hp1 HG00735.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-47248G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659054 | |||||||
chr2:163659073 | C | G | 4 | a0001c0001t0003g0193 a0001c0001t0015g0123 a0001c0001t0015g0124 others(1): Show |
4 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-47267G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659073 | |||||||
chr2:163659184 | G | C | 5 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 others(2): Show |
5 | HG02280.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-47378C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659184 | |||||||
chr2:163659261 | G | A | 1 | a0001c0001t0027g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.26-47455C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659261 | |||||||
chr2:163659270 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0027g0167 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.26-47464C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659270 | |||||||
chr2:163659504 | G | T | 1 | a0001c0001t0003g0116 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.26-47698C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659504 | |||||||
chr2:163659645 | C | T | 1 | a0001c0001t0071g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-47839G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659645 | |||||||
chr2:163659754 | C | G | 1 | a0001c0001t0053g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26-47948G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659754 | |||||||
chr2:163659802 | G | C | 4 | a0001c0001t0003g0193 a0001c0001t0015g0123 a0001c0001t0015g0124 others(1): Show |
4 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-47996C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163659802 | |||||||
chr2:163660101 | AAAAAAAT others(10): Show |
A | 1 | a0001c0001t0053g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26-48312_26-48296d others(19): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660101 | |||||||
chr2:163660288 | G | A | 51 | a0001c0001t0001g0043 a0001c0001t0001g0199 a0001c0001t0001g0200 others(48): Show |
51 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.26-48482C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660288 | |||||||
chr2:163660353 | T | C | 2 | a0001c0001t0004g0190 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-48547A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660353 | |||||||
chr2:163660528 | A | G | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-48722T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660528 | |||||||
chr2:163660562 | T | A | 65 | a0001c0001t0001g0043 a0001c0001t0001g0115 a0001c0001t0001g0176 others(62): Show |
66 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.26-48756A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660562 | |||||||
chr2:163660670 | C | CAT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
88 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.26-48866_26-48865d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660670 | |||||||
chr2:163660670 | CAT | C | 8 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-48866_26-48865d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660670 | |||||||
chr2:163660672 | TATATATA others(37): Show |
T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-48910_26-48867d others(46): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660672 | |||||||
chr2:163660679 | ATATATAC others(17): Show |
A | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-48897_26-48874d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660679 | |||||||
chr2:163660681 | A | ATACACAT others(57): Show |
2 | a0001c0001t0070g0103 a0001c0002t0007g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-48876_26-48875i others(66): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | |||||||
chr2:163660681 | A | ATATACAC others(15): Show |
19 | a0001c0001t0001g0228 a0001c0001t0001g0236 a0001c0001t0002g0050 others(16): Show |
19 | HG00408.hp2 HG00609.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-48897_26-48876d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | |||||||
chr2:163660681 | A | ATATACAC others(37): Show |
1 | a0001c0001t0002g0198 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.26-48919_26-48876d others(46): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | |||||||
chr2:163660681 | ATATACAC others(15): Show |
A | 8 | a0001c0001t0003g0193 a0001c0001t0004g0190 a0001c0001t0015g0123 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-48897_26-48876d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | |||||||
chr2:163660681 | ATATACAC others(37): Show |
A | 7 | a0001c0001t0001g0141 a0001c0001t0002g0205 a0001c0001t0014g0207 others(4): Show |
7 | HG00423.hp1 HG02155.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-48919_26-48876d others(46): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | |||||||
chr2:163660681 | ATATACAC others(59): Show |
A | 5 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(2): Show |
5 | HG00735.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-48941_26-48876d others(68): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660681 | |||||||
chr2:163660684 | T | C | 2 | a0001c0001t0006g0099 a0001c0002t0004g0185 |
2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26-48878A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660684 | |||||||
chr2:163660685 | ACACATAT others(33): Show |
A | 1 | a0001c0001t0077g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.26-48919_26-48880d others(42): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660685 | |||||||
chr2:163660686 | C | T | 2 | a0001c0001t0070g0103 a0001c0002t0007g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-48880G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660686 | |||||||
chr2:163660694 | C | T | 2 | a0001c0001t0035g0246 a0001c0008t0035g0248 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-48888G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660694 | |||||||
chr2:163660703 | G | A | 4 | a0001c0001t0002g0089 a0001c0001t0035g0246 a0001c0003t0002g0073 others(1): Show |
4 | NA18983.hp2 NA18988.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-48897C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660703 | |||||||
chr2:163660703 | GTATACAC others(125): Show |
G | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-49029_26-48898d others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660703 | |||||||
chr2:163660705 | ATACACAT others(175): Show |
A | 2 | a0001c0001t0035g0246 a0001c0008t0035g0248 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.26-49081_26-48900d others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660705 | |||||||
chr2:163660708 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.26-48902G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660708 | |||||||
chr2:163660713 | A | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0169 a0001c0001t0006g0170 |
3 | HG00140.hp2 HG01358.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.26-48907T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660713 | |||||||
chr2:163660716 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-48910G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660716 | |||||||
chr2:163660716 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-48934_26-48911d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660716 | |||||||
chr2:163660722 | T | A | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-48916A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660722 | |||||||
chr2:163660724 | TGTATACA others(127): Show |
T | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-49052_26-48919d others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660724 | |||||||
chr2:163660726 | T | C | 4 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0007g0182 others(1): Show |
4 | HG01106.hp1 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-48920A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660726 | |||||||
chr2:163660730 | C | CACATAT | 3 | a0001c0001t0019g0254 a0001c0001t0082g0258 a0001c0001t0083g0251 |
3 | HG00323.hp1 HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.26-48930_26-48925d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660730 | |||||||
chr2:163660730 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
111 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.26-48924G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660730 | |||||||
chr2:163660732 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26-48927_26-48926i others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660732 | |||||||
chr2:163660733 | A | G | 1 | a0001c0001t0005g0153 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.26-48927T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660733 | |||||||
chr2:163660752 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.26-48946G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660752 | |||||||
chr2:163660754 | C | CATATACA others(3): Show |
2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.26-48958_26-48949d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660754 | |||||||
chr2:163660755 | A | G | 2 | a0001c0001t0005g0153 a0001c0001t0005g0160 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-48949T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660755 | |||||||
chr2:163660768 | TGTATAC | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
84 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-48968_26-48963d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660768 | |||||||
chr2:163660769 | G | A | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48963C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660769 | |||||||
chr2:163660774 | C | T | 39 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0118 others(36): Show |
40 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.26-48968G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660774 | |||||||
chr2:163660774 | CACATATA others(27): Show |
C | 1 | a0001c0001t0001g0041 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.26-49002_26-48969d others(36): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660774 | |||||||
chr2:163660775 | A | G | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48969T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660775 | |||||||
chr2:163660776 | C | CATATACA others(3): Show |
3 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 |
3 | HG02896.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-48980_26-48971d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660776 | |||||||
chr2:163660776 | C | CATATACA others(35): Show |
1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.26-48971_26-48970i others(44): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660776 | |||||||
chr2:163660776 | C | T | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48970G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660776 | |||||||
chr2:163660777 | A | G | 3 | a0001c0001t0005g0153 a0001c0001t0005g0160 a0001c0001t0022g0083 |
3 | HG01978.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-48971T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660777 | |||||||
chr2:163660782 | C | T | 1 | a0001c0001t0021g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.26-48976G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660782 | |||||||
chr2:163660788 | T | C | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-48982A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660788 | |||||||
chr2:163660791 | G | A | 13 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0139 others(10): Show |
13 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-48985C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(205): Show |
1 | a0001c0001t0013g0101 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.26-48986_26-48985i others(214): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(185): Show |
1 | a0001c0002t0007g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.26-48986_26-48985i others(194): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(245): Show |
1 | a0001c0001t0005g0159 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(254): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(183): Show |
2 | a0001c0001t0003g0102 a0001c0002t0003g0100 |
2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.26-48986_26-48985i others(192): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(185): Show |
3 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0002t0007g0244 |
3 | HG01891.hp2 HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.26-48986_26-48985i others(194): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(209): Show |
1 | a0001c0001t0071g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(218): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(223): Show |
1 | a0001c0001t0021g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.26-48986_26-48985i others(232): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATACAC others(207): Show |
1 | a0001c0001t0005g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(216): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | G | GTATATAC others(207): Show |
1 | a0001c0001t0005g0153 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.26-48986_26-48985i others(216): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660791 | GTATATAG others(1): Show |
G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
84 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-48993_26-48986d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660791 | |||||||
chr2:163660792 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0176 others(7): Show |
10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-48986A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660792 | |||||||
chr2:163660796 | T | C | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-48990A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660796 | |||||||
chr2:163660798 | G | C | 36 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0118 others(33): Show |
37 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.26-48992C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660798 | |||||||
chr2:163660798 | G | T | 13 | a0001c0001t0001g0139 a0001c0001t0003g0102 a0001c0001t0003g0240 others(10): Show |
13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-48992C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660798 | |||||||
chr2:163660799 | A | ATATACAT others(183): Show |
5 | a0001c0001t0003g0097 a0001c0001t0023g0157 a0001c0001t0031g0091 others(2): Show |
5 | HG01175.hp1 HG01496.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-48994_26-48993i others(192): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660799 | |||||||
chr2:163660799 | A | ATATACAT others(183): Show |
1 | a0001c0001t0016g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.26-48994_26-48993i others(192): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660799 | |||||||
chr2:163660799 | A | G | 13 | a0001c0001t0001g0139 a0001c0001t0003g0102 a0001c0001t0003g0240 others(10): Show |
13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.26-48993T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660799 | |||||||
chr2:163660802 | TAC | T | 10 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0176 others(7): Show |
10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-48998_26-48997d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660802 | |||||||
chr2:163660808 | T | TATATGTA others(145): Show |
1 | a0001c0002t0007g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26-49003_26-49002i others(154): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660808 | |||||||
chr2:163660808 | T | TATATGTA others(167): Show |
2 | a0001c0002t0007g0135 a0001c0002t0028g0134 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26-49003_26-49002i others(176): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660808 | |||||||
chr2:163660809 | A | G | 10 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0176 others(7): Show |
10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-49003T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660809 | |||||||
chr2:163660810 | TATAC | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
83 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-49008_26-49005d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660810 | |||||||
chr2:163660813 | A | G | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-49007T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660813 | |||||||
chr2:163660814 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49008G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660814 | |||||||
chr2:163660815 | A | G | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.26-49009T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660815 | |||||||
chr2:163660816 | TATAC | T | 3 | a0001c0001t0022g0083 a0001c0001t0063g0234 a0003c0006t0009g0217 |
3 | HG01978.hp1 HG02132.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.26-49014_26-49011d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660816 | |||||||
chr2:163660818 | T | C | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-49012A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660818 | |||||||
chr2:163660820 | C | T | 12 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0176 others(9): Show |
12 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-49014G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660820 | |||||||
chr2:163660823 | A | ATATATGT others(9): Show |
3 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 |
3 | HG02896.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.26-49018_26-49017i others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660823 | |||||||
chr2:163660823 | A | G | 2 | a0001c0001t0031g0131 a0001c0002t0016g0132 |
2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-49017T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660823 | |||||||
chr2:163660826 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0176 others(7): Show |
10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-49020A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660826 | |||||||
chr2:163660828 | TGTATAC | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
82 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.26-49028_26-49023d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660828 | |||||||
chr2:163660829 | G | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0176 others(7): Show |
10 | HG01106.hp1 HG01515.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.26-49023C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660829 | |||||||
chr2:163660830 | T | TATATACA others(231): Show |
1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.26-49025_26-49024i others(240): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660830 | |||||||
chr2:163660834 | C | CAT | 47 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(44): Show |
47 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-49030_26-49029d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660834 | |||||||
chr2:163660834 | C | CATAT | 25 | a0001c0001t0001g0118 a0001c0001t0001g0139 a0001c0001t0003g0097 others(22): Show |
26 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-49032_26-49029d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660834 | |||||||
chr2:163660834 | C | T | 12 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0176 others(9): Show |
12 | HG00639.hp1 HG01106.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-49028G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660834 | |||||||
chr2:163660837 | A | ATATACAT others(7): Show |
1 | a0001c0001t0003g0116 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.26-49032_26-49031i others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | |||||||
chr2:163660837 | A | ATATATAT others(13): Show |
2 | a0001c0001t0070g0103 a0001c0002t0007g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.26-49032_26-49031i others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | |||||||
chr2:163660837 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.26-49031T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | |||||||
chr2:163660837 | ATATACAT others(9): Show |
A | 1 | a0003c0006t0009g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.26-49047_26-49032d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | |||||||
chr2:163660837 | ATATACAT others(44): Show |
A | 1 | a0001c0001t0077g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.26-49082_26-49032d others(53): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660837 | |||||||
chr2:163660840 | TACATATA others(11): Show |
T | 1 | a0001c0001t0063g0234 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.26-49052_26-49035d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660840 | |||||||
chr2:163660842 | C | T | 6 | a0001c0001t0002g0058 a0001c0001t0014g0015 a0001c0001t0022g0083 others(3): Show |
6 | HG01978.hp1 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49036G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660842 | |||||||
chr2:163660844 | T | C | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-49038A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660844 | |||||||
chr2:163660844 | T | TAC | 3 | a0001c0002t0007g0135 a0001c0002t0007g0136 a0001c0002t0028g0134 |
3 | HG03225.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.26-49039_26-49038i others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660844 | |||||||
chr2:163660845 | A | G | 3 | a0001c0001t0002g0058 a0001c0001t0014g0015 a0001c0001t0022g0083 |
3 | HG01978.hp1 HG03688.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.26-49039T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660845 | |||||||
chr2:163660850 | T | C | 3 | a0001c0001t0002g0058 a0001c0001t0014g0015 a0001c0001t0022g0083 |
3 | HG01978.hp1 HG03688.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.26-49044A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660850 | |||||||
chr2:163660853 | G | A | 8 | a0001c0001t0002g0058 a0001c0001t0003g0106 a0001c0001t0003g0116 others(5): Show |
8 | HG01978.hp1 HG02280.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-49047C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660853 | |||||||
chr2:163660854 | T | A | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-49048A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660854 | |||||||
chr2:163660858 | C | CAT | 3 | a0001c0001t0013g0101 a0001c0001t0024g0001 a0001c0001t0050g0172 |
4 | HG02559.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-49054_26-49053d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660858 | C | CATAT | 5 | a0001c0001t0001g0115 a0001c0001t0003g0102 a0001c0001t0011g0114 others(2): Show |
5 | HG00735.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-49056_26-49053d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660858 | C | CATATAT | 7 | a0001c0001t0005g0174 a0001c0001t0013g0194 a0001c0001t0031g0091 others(4): Show |
7 | HG01175.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-49058_26-49053d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660858 | C | CATATATA others(1): Show |
4 | a0001c0001t0001g0139 a0001c0001t0005g0159 a0001c0001t0016g0130 others(1): Show |
4 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49060_26-49053d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660858 | C | CATATATA others(3): Show |
1 | a0001c0001t0071g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-49062_26-49053d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660858 | C | CATATATA others(5): Show |
1 | a0001c0001t0021g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.26-49064_26-49053d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660858 | C | T | 9 | a0001c0001t0002g0058 a0001c0001t0003g0106 a0001c0001t0003g0116 others(6): Show |
9 | HG01978.hp1 HG02132.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-49052G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660858 | CAT | C | 4 | a0001c0001t0001g0220 a0001c0001t0003g0162 a0001c0001t0008g0060 others(1): Show |
4 | HG01496.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49054_26-49053d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660858 | |||||||
chr2:163660863 | A | G | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-49057T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660863 | |||||||
chr2:163660865 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0006g0099 a0001c0001t0008g0072 |
3 | HG02055.hp2 NA18747.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.26-49059T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660865 | |||||||
chr2:163660865 | A | T | 1 | a0001c0001t0012g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.26-49059T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660865 | |||||||
chr2:163660867 | A | G | 3 | a0001c0001t0004g0133 a0001c0001t0004g0190 a0001c0002t0013g0191 |
3 | HG02976.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-49061T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660867 | |||||||
chr2:163660871 | A | G | 3 | a0001c0001t0002g0058 a0001c0001t0014g0015 a0001c0001t0022g0083 |
3 | HG01978.hp1 HG03688.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.26-49065T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660871 | |||||||
chr2:163660873 | A | G | 2 | a0001c0001t0004g0190 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-49067T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660873 | |||||||
chr2:163660877 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0042 |
2 | HG01167.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.26-49071T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660877 | |||||||
chr2:163660878 | TA | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
82 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.26-49073delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660878 | |||||||
chr2:163660879 | A | AT | 6 | a0001c0001t0003g0106 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49074dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | A | ATATAT | 8 | a0001c0001t0001g0200 a0001c0001t0001g0236 a0001c0001t0006g0235 others(5): Show |
8 | HG00609.hp1 NA18941.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | A | ATATATAT others(18): Show |
1 | a0001c0001t0005g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.26-49074_26-49073i others(27): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | A | ATATATT | 6 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0201 others(3): Show |
6 | HG02056.hp1 HG02109.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | A | ATATTT | 5 | a0001c0001t0002g0229 a0001c0001t0003g0187 a0001c0001t0015g0126 others(2): Show |
5 | HG00408.hp2 HG02129.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | A | ATATTTT | 11 | a0001c0001t0001g0219 a0001c0001t0002g0004 a0001c0001t0002g0203 others(8): Show |
11 | HG00423.hp1 HG02630.hp1 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-49074_26-49073i others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0038 |
2 | HG02015.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.26-49073T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | A | T | 1 | a0001c0002t0011g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.26-49073T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | AT | A | 34 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0137 others(31): Show |
34 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-49074delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660879 | ATT | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0140 a0001c0001t0001g0141 others(20): Show |
23 | HG00140.hp1 HG00558.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.26-49075_26-49074d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660879 | |||||||
chr2:163660880 | T | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(73): Show |
76 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.26-49074A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | |||||||
chr2:163660880 | T | TATATA | 3 | a0001c0001t0002g0223 a0001c0001t0003g0097 a0001c0001t0070g0103 |
3 | HG02027.hp2 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.26-49075_26-49074i others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | |||||||
chr2:163660880 | T | TATATATA | 4 | a0001c0001t0005g0153 a0001c0001t0005g0160 a0001c0004t0033g0138 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49075_26-49074i others(9): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | |||||||
chr2:163660880 | T | TATATATA others(12): Show |
1 | a0001c0001t0006g0239 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.26-49075_26-49074i others(21): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | |||||||
chr2:163660880 | T | TG | 7 | a0001c0001t0001g0118 a0001c0001t0002g0005 a0001c0001t0003g0105 others(4): Show |
7 | HG00408.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-49075_26-49074i others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660880 | |||||||
chr2:163660881 | T | A | 19 | a0001c0001t0001g0115 a0001c0001t0002g0019 a0001c0001t0002g0038 others(16): Show |
20 | HG01175.hp1 HG01261.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-49075A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660881 | |||||||
chr2:163660881 | T | G | 1 | a0001c0001t0008g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.26-49075A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660881 | |||||||
chr2:163660882 | T | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.26-49076A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660882 | |||||||
chr2:163660883 | T | A | 24 | a0001c0001t0001g0158 a0001c0001t0001g0176 a0001c0001t0002g0019 others(21): Show |
25 | HG00558.hp2 HG01106.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-49077A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660883 | |||||||
chr2:163660884 | T | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.26-49078A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660884 | |||||||
chr2:163660885 | T | A | 15 | a0001c0001t0002g0019 a0001c0001t0002g0038 a0001c0001t0003g0102 others(12): Show |
16 | HG02015.hp2 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-49079A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660885 | |||||||
chr2:163660886 | T | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.26-49080A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660886 | |||||||
chr2:163660887 | T | A | 7 | a0001c0001t0002g0019 a0001c0001t0002g0038 a0001c0001t0008g0060 others(4): Show |
7 | HG02015.hp2 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-49081A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660887 | |||||||
chr2:163660888 | T | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
85 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-49082A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660888 | |||||||
chr2:163660889 | T | A | 6 | a0001c0001t0002g0019 a0001c0001t0002g0038 a0001c0001t0008g0060 others(3): Show |
6 | HG02015.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-49083A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660889 | |||||||
chr2:163660890 | T | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0055 a0001c0001t0002g0074 others(6): Show |
9 | HG01884.hp2 HG02074.hp2 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-49084A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163660890 | |||||||
chr2:163661033 | G | A | 2 | a0001c0001t0007g0020 a0001c0002t0016g0067 |
2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.26-49227C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661033 | |||||||
chr2:163661233 | T | TTTA | 4 | a0001c0001t0030g0096 a0001c0002t0007g0135 a0001c0002t0007g0136 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-49430_26-49428d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661233 | |||||||
chr2:163661519 | C | G | 5 | a0001c0001t0001g0119 a0001c0001t0003g0105 a0001c0001t0004g0192 others(2): Show |
5 | HG01891.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-49713G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661519 | |||||||
chr2:163661657 | T | C | 1 | a0001c0002t0007g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.26-49851A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661657 | |||||||
chr2:163661774 | G | A | 1 | a0001c0001t0041g0030 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.26-49968C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661774 | |||||||
chr2:163661784 | T | C | 5 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 others(2): Show |
5 | HG02280.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-49978A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661784 | |||||||
chr2:163661786 | T | G | 6 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0005g0117 others(3): Show |
6 | HG02280.hp2 HG02735.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-49980A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661786 | |||||||
chr2:163661808 | G | T | 2 | a0001c0001t0002g0229 a0001c0001t0052g0218 |
2 | HG00408.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.26-50002C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661808 | |||||||
chr2:163661822 | A | T | 3 | a0001c0001t0004g0133 a0001c0001t0006g0099 a0001c0002t0004g0185 |
3 | HG02055.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.26-50016T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661822 | |||||||
chr2:163661875 | A | G | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-50069T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661875 | |||||||
chr2:163661888 | C | T | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01175.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-50082G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661888 | |||||||
chr2:163661899 | T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.26-50093A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163661899 | |||||||
chr2:163662027 | T | C | 4 | a0001c0001t0030g0096 a0001c0002t0007g0135 a0001c0002t0007g0136 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-50221A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662027 | |||||||
chr2:163662039 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-50233C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662039 | |||||||
chr2:163662133 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.26-50327A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662133 | |||||||
chr2:163662202 | G | A | 1 | a0001c0001t0004g0085 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-50396C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662202 | |||||||
chr2:163662267 | A | G | 2 | a0001c0001t0003g0105 a0001c0001t0004g0192 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.26-50461T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662267 | |||||||
chr2:163662421 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0005g0153 a0001c0001t0005g0159 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-50615C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662421 | |||||||
chr2:163662542 | T | G | 3 | a0001c0001t0001g0119 a0001c0001t0024g0001 a0001c0002t0009g0120 |
4 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-50736A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662542 | |||||||
chr2:163662598 | G | A | 1 | a0001c0001t0020g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.26-50792C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662598 | |||||||
chr2:163662655 | T | G | 2 | a0001c0001t0001g0118 a0001c0002t0004g0185 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.26-50849A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662655 | |||||||
chr2:163662771 | G | A | 45 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(42): Show |
45 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.26-50965C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163662771 | |||||||
chr2:163663325 | T | TTTTG | 17 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(14): Show |
17 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-51523_26-51520d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663325 | |||||||
chr2:163663365 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.26-51559C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663365 | |||||||
chr2:163663518 | G | A | 2 | a0001c0001t0003g0105 a0001c0001t0004g0192 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.26-51712C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663518 | |||||||
chr2:163663605 | G | A | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.26-51799C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663605 | |||||||
chr2:163663898 | G | GA | 28 | a0001c0001t0001g0137 a0001c0001t0003g0106 a0001c0001t0003g0116 others(25): Show |
28 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.26-52093dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663898 | |||||||
chr2:163663911 | T | C | 112 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0137 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.26-52105A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663911 | |||||||
chr2:163663925 | G | A | 2 | a0001c0001t0029g0022 a0001c0001t0051g0084 |
2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.26-52119C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163663925 | |||||||
chr2:163664138 | T | C | 1 | a0001c0001t0014g0025 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.26-52332A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664138 | |||||||
chr2:163664258 | C | G | 2 | a0001c0001t0004g0190 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.26-52452G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664258 | |||||||
chr2:163664269 | C | A | 1 | a0001c0001t0025g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-52463G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664269 | |||||||
chr2:163664342 | T | C | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.26-52536A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664342 | |||||||
chr2:163664485 | C | T | 1 | a0001c0004t0033g0138 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.26-52679G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664485 | |||||||
chr2:163664591 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.26-52785G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664591 | |||||||
chr2:163664984 | T | C | 2 | a0001c0001t0003g0105 a0001c0001t0004g0192 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.26-53178A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664984 | |||||||
chr2:163664998 | G | GT | 85 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0140 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-53193dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163664998 | |||||||
chr2:163665005 | A | G | 4 | a0001c0001t0025g0109 a0001c0001t0027g0107 a0001c0001t0045g0177 others(1): Show |
4 | HG02723.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-53199T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665005 | |||||||
chr2:163665034 | G | A | 16 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0001c0001t0001g0176 others(13): Show |
16 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-53228C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665034 | |||||||
chr2:163665242 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.26-53436G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665242 | |||||||
chr2:163665384 | C | T | 2 | a0001c0001t0015g0126 a0001c0001t0030g0127 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.26-53578G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665384 | |||||||
chr2:163665556 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.26-53750A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665556 | |||||||
chr2:163665892 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.26-54086G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163665892 | |||||||
chr2:163666055 | A | G | 1 | a0001c0001t0026g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.26-54249T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666055 | |||||||
chr2:163666398 | A | G | 3 | a0001c0001t0003g0106 a0001c0001t0004g0190 a0001c0002t0007g0244 |
3 | HG02630.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.26-54592T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666398 | |||||||
chr2:163666442 | G | A | 21 | a0001c0001t0001g0016 a0001c0001t0001g0140 a0001c0001t0001g0141 others(18): Show |
21 | HG00140.hp1 HG00558.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.26-54636C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666442 | |||||||
chr2:163666690 | G | A | 1 | a0001c0001t0004g0085 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-54884C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666690 | |||||||
chr2:163666717 | T | C | 12 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-54911A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666717 | |||||||
chr2:163666765 | GC | G | 17 | a0001c0001t0001g0228 a0001c0001t0001g0236 a0001c0001t0002g0223 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.26-54960delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666765 | |||||||
chr2:163666766 | C | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(239): Show |
243 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.26-54960G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666766 | |||||||
chr2:163666894 | A | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-55088T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666894 | |||||||
chr2:163666901 | T | TA | 125 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0098 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.26-55096dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163666901 | |||||||
chr2:163667235 | C | A | 25 | a0001c0001t0001g0137 a0001c0001t0003g0116 a0001c0001t0005g0117 others(22): Show |
25 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.26-55429G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667235 | |||||||
chr2:163667291 | C | T | 88 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0139 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.26-55485G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667291 | |||||||
chr2:163667338 | C | CA | 111 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0118 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.26-55533dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667338 | |||||||
chr2:163667338 | C | CAA | 34 | a0001c0001t0001g0016 a0001c0001t0001g0098 a0001c0001t0001g0110 others(31): Show |
34 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.26-55534_26-55533d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667338 | |||||||
chr2:163667338 | C | CAAA | 21 | a0001c0001t0001g0137 a0001c0001t0003g0116 a0001c0001t0005g0117 others(18): Show |
21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.26-55535_26-55533d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667338 | |||||||
chr2:163667503 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.26-55697A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667503 | |||||||
chr2:163667579 | T | C | 3 | a0001c0001t0021g0184 a0001c0001t0050g0172 a0001c0002t0013g0191 |
3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-55773A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667579 | |||||||
chr2:163667726 | A | G | 1 | a0001c0001t0060g0059 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-55920T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667726 | |||||||
chr2:163667740 | G | A | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-55934C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667740 | |||||||
chr2:163667809 | A | G | 1 | a0001c0001t0083g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.26-56003T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667809 | |||||||
chr2:163667883 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-56077C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667883 | |||||||
chr2:163667913 | G | A | 4 | a0001c0001t0030g0096 a0001c0002t0007g0135 a0001c0002t0007g0136 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-56107C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667913 | |||||||
chr2:163667952 | C | T | 2 | a0001c0001t0002g0205 a0001c0001t0014g0207 |
2 | HG00423.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.26-56146G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163667952 | |||||||
chr2:163668014 | A | AC | 30 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0003g0183 others(27): Show |
30 | HG00423.hp2 HG00558.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.26-56209dupG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | |||||||
chr2:163668014 | A | ACC | 25 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(22): Show |
25 | HG01106.hp1 HG01515.hp2 HG02293.hp1 others(22): Show |
intron_variant | MODIFIER | c.26-56210_26-56209d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | |||||||
chr2:163668014 | A | ACCC | 42 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0158 others(39): Show |
42 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.26-56211_26-56209d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | |||||||
chr2:163668014 | A | ACCCC | 30 | a0001c0001t0001g0016 a0001c0001t0001g0143 a0001c0001t0001g0152 others(27): Show |
30 | HG00140.hp2 HG00423.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.26-56212_26-56209d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668014 | |||||||
chr2:163668023 | C | G | 2 | a0001c0001t0001g0002 a0001c0001t0012g0071 |
2 | HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.26-56217G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668023 | |||||||
chr2:163668025 | C | CA | 3 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0016g0132 |
3 | HG02280.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.26-56220dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668025 | |||||||
chr2:163668026 | A | C | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-56220T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668026 | |||||||
chr2:163668229 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.26-56423C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668229 | |||||||
chr2:163668316 | A | C | 11 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-56510T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668316 | |||||||
chr2:163668355 | G | A | 20 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0106 others(17): Show |
20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-56549C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668355 | |||||||
chr2:163668525 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.26-56719G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668525 | |||||||
chr2:163668739 | G | A | 2 | a0001c0001t0041g0030 a0001c0001t0073g0011 |
2 | HG02135.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.26-56933C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668739 | |||||||
chr2:163668935 | C | T | 2 | a0001c0001t0005g0153 a0001c0001t0005g0160 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.26-57129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668935 | |||||||
chr2:163668970 | T | C | 2 | a0001c0001t0015g0126 a0001c0001t0030g0127 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.26-57164A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163668970 | |||||||
chr2:163669015 | A | AAT | 112 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0043 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.26-57211_26-57210d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATAT | 5 | a0001c0001t0002g0142 a0001c0001t0026g0094 a0001c0001t0035g0246 others(2): Show |
5 | HG02647.hp2 NA18946.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-57213_26-57210d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATAT | 8 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(5): Show |
8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-57215_26-57210d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(1): Show |
2 | a0001c0001t0001g0152 a0001c0001t0003g0105 |
2 | HG02818.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.26-57217_26-57210d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(3): Show |
5 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG02698.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-57219_26-57210d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(5): Show |
7 | a0001c0001t0003g0106 a0001c0001t0003g0116 a0001c0001t0004g0190 others(4): Show |
7 | HG01496.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-57221_26-57210d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(7): Show |
8 | a0001c0001t0059g0093 a0001c0002t0007g0104 a0001c0002t0007g0135 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-57223_26-57210d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(9): Show |
7 | a0001c0001t0003g0102 a0001c0001t0003g0240 a0001c0001t0005g0174 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-57225_26-57210d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(11): Show |
2 | a0001c0001t0013g0101 a0001c0001t0013g0194 |
2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.26-57227_26-57210d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(13): Show |
2 | a0001c0001t0003g0097 a0001c0001t0006g0239 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.26-57229_26-57210d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(15): Show |
5 | a0001c0001t0001g0118 a0001c0001t0006g0099 a0001c0001t0007g0182 others(2): Show |
5 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-57210_26-57209i others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(17): Show |
3 | a0001c0001t0001g0176 a0001c0001t0011g0173 a0001c0001t0021g0243 |
3 | HG01106.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.26-57210_26-57209i others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | A | AATATATA others(19): Show |
2 | a0001c0001t0003g0183 a0001c0002t0007g0244 |
2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.26-57210_26-57209i others(28): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669015 | AAT | A | 6 | a0001c0001t0001g0002 a0001c0001t0019g0261 a0001c0001t0019g0262 others(3): Show |
6 | HG01175.hp2 HG01361.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-57211_26-57210d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669015 | |||||||
chr2:163669035 | T | TATATATA others(5): Show |
3 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0058g0155 |
3 | HG00558.hp1 NA18951.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.26-57230_26-57229i others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669035 | |||||||
chr2:163669073 | A | G | 1 | a0001c0001t0023g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-57267T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669073 | |||||||
chr2:163669116 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.26-57310T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669116 | |||||||
chr2:163669143 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.26-57337G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669143 | |||||||
chr2:163669288 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.26-57482C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669288 | |||||||
chr2:163669360 | T | C | 1 | a0001c0001t0006g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-57554A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669360 | |||||||
chr2:163669464 | C | G | 1 | a0001c0001t0053g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.26-57658G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669464 | |||||||
chr2:163669585 | G | GTAGAT | 8 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-57784_26-57780d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669585 | |||||||
chr2:163669791 | C | A | 1 | a0001c0001t0057g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-57985G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669791 | |||||||
chr2:163669922 | C | T | 1 | a0001c0001t0039g0231 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.26-58116G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163669922 | |||||||
chr2:163670075 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.26-58269T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670075 | |||||||
chr2:163670177 | C | T | 20 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0116 others(17): Show |
20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-58371G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670177 | |||||||
chr2:163670249 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-58443G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670249 | |||||||
chr2:163670315 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.26-58509T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670315 | |||||||
chr2:163670550 | A | G | 3 | a0001c0001t0021g0184 a0001c0001t0050g0172 a0001c0002t0013g0191 |
3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-58744T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670550 | |||||||
chr2:163670587 | A | T | 1 | a0001c0001t0010g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.26-58781T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670587 | |||||||
chr2:163670589 | T | G | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-58783A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670589 | |||||||
chr2:163670591 | T | A | 1 | a0001c0001t0010g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.26-58785A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670591 | |||||||
chr2:163670592 | A | G | 1 | a0001c0001t0010g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.26-58786T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670592 | |||||||
chr2:163670917 | G | A | 1 | a0001c0001t0070g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.26-59111C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163670917 | |||||||
chr2:163671073 | G | A | 2 | a0001c0001t0004g0225 a0001c0001t0004g0226 |
2 | NA18951.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.26-59267C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671073 | |||||||
chr2:163671121 | G | A | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-59315C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671121 | |||||||
chr2:163671228 | C | G | 6 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0001t0021g0243 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-59422G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671228 | |||||||
chr2:163671462 | G | T | 7 | a0001c0001t0004g0133 a0001c0001t0030g0096 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-59656C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671462 | |||||||
chr2:163671600 | TA | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.26-59795delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671600 | |||||||
chr2:163671602 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.26-59796C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163671602 | |||||||
chr2:163672251 | T | TA | 103 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0118 others(100): Show |
103 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.26-60446dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672251 | |||||||
chr2:163672251 | T | TAA | 32 | a0001c0001t0001g0043 a0001c0001t0001g0137 a0001c0001t0002g0223 others(29): Show |
32 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.26-60447_26-60446d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672251 | |||||||
chr2:163672251 | TA | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0078 others(14): Show |
17 | HG00408.hp1 HG01884.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-60446delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672251 | |||||||
chr2:163672341 | G | T | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-60535C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672341 | |||||||
chr2:163672462 | A | G | 6 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0001t0021g0243 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-60656T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672462 | |||||||
chr2:163672560 | T | C | 20 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0106 others(17): Show |
20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.26-60754A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672560 | |||||||
chr2:163672878 | AATGAG | A | 2 | a0001c0001t0003g0106 a0001c0001t0004g0190 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.26-61077_26-61073d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672878 | |||||||
chr2:163672891 | T | C | 3 | a0001c0001t0021g0184 a0001c0001t0050g0172 a0001c0002t0013g0191 |
3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.26-61085A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163672891 | |||||||
chr2:163673018 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.26-61212G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673018 | |||||||
chr2:163673134 | C | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.26-61328G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673134 | |||||||
chr2:163673223 | G | A | 25 | a0001c0001t0001g0137 a0001c0001t0003g0116 a0001c0001t0005g0117 others(22): Show |
25 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.26-61417C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673223 | |||||||
chr2:163673265 | C | T | 1 | a0001c0001t0055g0044 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.26-61459G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673265 | |||||||
chr2:163673266 | G | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.26-61460C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673266 | |||||||
chr2:163673682 | T | C | 113 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0137 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.25+61221A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673682 | |||||||
chr2:163673748 | T | C | 22 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0106 others(19): Show |
22 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+61155A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163673748 | |||||||
chr2:163674166 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.25+60737T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674166 | |||||||
chr2:163674239 | T | C | 1 | a0001c0001t0012g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+60664A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674239 | |||||||
chr2:163674273 | C | A | 12 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+60630G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674273 | |||||||
chr2:163674273 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+60630G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674273 | |||||||
chr2:163674295 | TTG | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02698.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+60606_25+60607d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674295 | |||||||
chr2:163674326 | T | A | 12 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+60577A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674326 | |||||||
chr2:163674365 | T | C | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+60538A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674365 | |||||||
chr2:163674650 | A | G | 1 | a0001c0001t0006g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+60253T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674650 | |||||||
chr2:163674694 | G | A | 14 | a0001c0001t0001g0046 a0001c0001t0002g0019 a0001c0001t0002g0035 others(11): Show |
14 | HG00408.hp1 HG01884.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.25+60209C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674694 | |||||||
chr2:163674705 | T | C | 12 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+60198A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674705 | |||||||
chr2:163674737 | G | A | 44 | a0001c0001t0001g0016 a0001c0001t0001g0139 a0001c0001t0001g0140 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.25+60166C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674737 | |||||||
chr2:163674795 | T | A | 93 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0139 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.25+60108A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674795 | |||||||
chr2:163674936 | C | A | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+59967G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163674936 | |||||||
chr2:163675036 | A | G | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+59867T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675036 | |||||||
chr2:163675352 | A | G | 169 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0098 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.25+59551T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675352 | |||||||
chr2:163675427 | A | G | 1 | a0001c0001t0012g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.25+59476T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675427 | |||||||
chr2:163675453 | T | C | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+59450A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675453 | |||||||
chr2:163675478 | T | C | 4 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0007g0182 others(1): Show |
4 | HG01106.hp1 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+59425A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675478 | |||||||
chr2:163675504 | G | A | 2 | a0001c0001t0003g0193 a0001c0001t0004g0192 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+59399C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675504 | |||||||
chr2:163675653 | C | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0002g0005 others(2): Show |
5 | NA18964.hp1 NA18969.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+59250G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675653 | |||||||
chr2:163675706 | C | CT | 37 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0119 others(34): Show |
37 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.25+59196dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675706 | |||||||
chr2:163675706 | CT | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0041 others(29): Show |
32 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.25+59196delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675706 | |||||||
chr2:163675706 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+59187_25+59196d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675706 | |||||||
chr2:163675711 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0070g0103 a0001c0002t0007g0104 |
3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+59192A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675711 | |||||||
chr2:163675775 | C | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(77): Show |
80 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.25+59128G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675775 | |||||||
chr2:163675918 | G | A | 3 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0016g0132 |
3 | HG02280.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.25+58985C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163675918 | |||||||
chr2:163676016 | C | G | 1 | a0001c0003t0068g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.25+58887G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676016 | |||||||
chr2:163676029 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+58874A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676029 | |||||||
chr2:163676033 | G | A | 2 | a0001c0001t0003g0106 a0001c0001t0004g0190 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+58870C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676033 | |||||||
chr2:163676089 | C | A | 4 | a0001c0001t0030g0096 a0001c0002t0007g0135 a0001c0002t0007g0136 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+58814G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676089 | |||||||
chr2:163676116 | C | G | 1 | a0001c0001t0029g0022 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.25+58787G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676116 | |||||||
chr2:163676270 | C | A | 44 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(41): Show |
44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+58633G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676270 | |||||||
chr2:163676434 | A | AAT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0082 others(8): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+58467_25+58468d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | A | AATAT | 6 | a0001c0001t0001g0158 a0001c0001t0002g0144 a0001c0001t0005g0159 others(3): Show |
6 | HG00558.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+58465_25+58468d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | A | AATATAT | 6 | a0001c0001t0001g0118 a0001c0001t0001g0141 a0001c0001t0002g0026 others(3): Show |
6 | HG01978.hp2 HG02132.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+58463_25+58468d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | A | AATATATA others(3): Show |
1 | a0001c0001t0031g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.25+58459_25+58468d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AAT | A | 24 | a0001c0001t0001g0110 a0001c0001t0001g0137 a0001c0001t0001g0139 others(21): Show |
24 | HG00558.hp1 HG01255.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+58467_25+58468d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATAT | A | 21 | a0001c0001t0001g0016 a0001c0001t0001g0111 a0001c0001t0001g0152 others(18): Show |
21 | HG00140.hp2 HG01358.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+58465_25+58468d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATAT | A | 14 | a0001c0001t0004g0192 a0001c0001t0005g0153 a0001c0001t0015g0126 others(11): Show |
14 | HG02486.hp1 HG02895.hp2 HG03130.hp2 others(11): Show |
intron_variant | MODIFIER | c.25+58463_25+58468d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(1): Show |
A | 4 | a0001c0001t0003g0193 a0001c0001t0003g0240 a0001c0001t0004g0133 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+58461_25+58468d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(3): Show |
A | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.25+58459_25+58468d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(5): Show |
A | 2 | a0001c0001t0007g0182 a0001c0002t0016g0132 |
2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.25+58457_25+58468d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(7): Show |
A | 10 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0105 others(7): Show |
10 | HG01106.hp1 HG02280.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+58455_25+58468d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(9): Show |
A | 9 | a0001c0001t0003g0116 a0001c0001t0003g0187 a0001c0001t0005g0117 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+58453_25+58468d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(11): Show |
A | 6 | a0001c0001t0001g0115 a0001c0001t0002g0146 a0001c0001t0002g0150 others(3): Show |
6 | HG00735.hp2 HG01891.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+58451_25+58468d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(13): Show |
A | 1 | a0001c0002t0028g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+58449_25+58468d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676434 | AATATATA others(19): Show |
A | 44 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(41): Show |
44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+58443_25+58468d others(28): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676434 | |||||||
chr2:163676454 | TATATATA others(23): Show |
T | 5 | a0001c0001t0001g0119 a0001c0001t0016g0130 a0001c0001t0024g0001 others(2): Show |
6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+58419_25+58448d others(32): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676454 | |||||||
chr2:163676456 | TATATATA others(21): Show |
T | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.25+58419_25+58446d others(30): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676456 | |||||||
chr2:163676463 | A | C | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+58440T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676463 | |||||||
chr2:163676464 | TATATATA others(13): Show |
T | 2 | a0001c0001t0001g0002 a0001c0002t0013g0191 |
2 | HG01175.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+58419_25+58438d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676464 | |||||||
chr2:163676466 | T | TATATATA others(28): Show |
1 | a0001c0001t0021g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25+58436_25+58437i others(37): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676466 | |||||||
chr2:163676466 | T | TATATATA others(24): Show |
1 | a0001c0001t0050g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+58436_25+58437i others(33): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676466 | |||||||
chr2:163676470 | TATATATA others(7): Show |
T | 1 | a0001c0001t0078g0057 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+58419_25+58432d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676470 | |||||||
chr2:163676472 | TATATATA others(5): Show |
T | 1 | a0001c0001t0008g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.25+58419_25+58430d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676472 | |||||||
chr2:163676476 | TATATATA others(1): Show |
T | 6 | a0001c0001t0001g0055 a0001c0001t0002g0005 a0001c0001t0002g0050 others(3): Show |
6 | HG03669.hp2 HG03927.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+58419_25+58426d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676476 | |||||||
chr2:163676478 | TATATAA | T | 11 | a0001c0001t0001g0046 a0001c0001t0001g0077 a0001c0001t0002g0075 others(8): Show |
11 | HG00323.hp2 HG00408.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+58419_25+58424d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676478 | |||||||
chr2:163676480 | TATAA | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0042 others(13): Show |
16 | HG01257.hp2 HG01261.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+58419_25+58422d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676480 | |||||||
chr2:163676482 | TAA | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(24): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.25+58419_25+58420d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676482 | |||||||
chr2:163676484 | A | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(21): Show |
24 | HG00741.hp1 HG01071.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+58419T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676484 | |||||||
chr2:163676923 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+57980T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163676923 | |||||||
chr2:163677348 | A | T | 87 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0139 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.25+57555T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677348 | |||||||
chr2:163677377 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.25+57526A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677377 | |||||||
chr2:163677581 | T | C | 7 | a0001c0001t0004g0133 a0001c0001t0030g0096 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+57322A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677581 | |||||||
chr2:163677734 | T | C | 1 | a0001c0001t0014g0207 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.25+57169A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677734 | |||||||
chr2:163677924 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
108 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.25+56979C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163677924 | |||||||
chr2:163678346 | G | A | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+56557C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678346 | |||||||
chr2:163678427 | G | C | 1 | a0001c0001t0026g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.25+56476C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678427 | |||||||
chr2:163678512 | C | T | 1 | a0001c0001t0023g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.25+56391G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678512 | |||||||
chr2:163678548 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.25+56355A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678548 | |||||||
chr2:163678664 | G | C | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+56239C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678664 | |||||||
chr2:163678958 | T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.25+55945A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163678958 | |||||||
chr2:163679220 | G | A | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+55683C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679220 | |||||||
chr2:163679259 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+55644G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679259 | |||||||
chr2:163679260 | G | A | 2 | a0001c0001t0070g0103 a0001c0002t0007g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+55643C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679260 | |||||||
chr2:163679338 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+55565A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679338 | |||||||
chr2:163679365 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(7): Show |
10 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+55538C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679365 | |||||||
chr2:163679474 | C | T | 11 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+55429G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679474 | |||||||
chr2:163679495 | C | CA | 101 | a0001c0001t0001g0016 a0001c0001t0001g0098 a0001c0001t0001g0118 others(98): Show |
101 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.25+55407dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679495 | |||||||
chr2:163679495 | C | CAA | 41 | a0001c0001t0001g0043 a0001c0001t0001g0152 a0001c0001t0001g0196 others(38): Show |
41 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.25+55406_25+55407d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679495 | |||||||
chr2:163679495 | C | CAAA | 5 | a0001c0001t0001g0228 a0001c0001t0006g0235 a0001c0001t0062g0227 others(2): Show |
5 | HG02056.hp1 NA18988.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+55405_25+55407d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679495 | |||||||
chr2:163679511 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+55392A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679511 | |||||||
chr2:163679668 | G | A | 4 | a0001c0001t0030g0096 a0001c0002t0007g0135 a0001c0002t0007g0136 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+55235C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679668 | |||||||
chr2:163679812 | C | T | 7 | a0001c0001t0004g0133 a0001c0001t0030g0096 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+55091G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679812 | |||||||
chr2:163679940 | G | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0164 a0001c0001t0027g0167 |
3 | HG03669.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.25+54963C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679940 | |||||||
chr2:163679980 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.25+54923C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163679980 | |||||||
chr2:163680309 | A | G | 2 | a0001c0001t0009g0128 a0001c0002t0011g0129 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+54594T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680309 | |||||||
chr2:163680350 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.25+54553G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680350 | |||||||
chr2:163680356 | A | G | 35 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(32): Show |
35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+54547T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680356 | |||||||
chr2:163680376 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
82 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.25+54527C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680376 | |||||||
chr2:163680386 | C | G | 4 | a0001c0001t0030g0096 a0001c0002t0007g0135 a0001c0002t0007g0136 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+54517G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680386 | |||||||
chr2:163680512 | G | A | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25+54391C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680512 | |||||||
chr2:163680710 | A | G | 2 | a0001c0001t0006g0235 a0001c0001t0062g0227 |
2 | NA19076.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.25+54193T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680710 | |||||||
chr2:163680732 | C | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+54171G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680732 | |||||||
chr2:163680874 | A | G | 1 | a0001c0001t0072g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.25+54029T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680874 | |||||||
chr2:163680946 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(92): Show |
96 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.25+53957A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680946 | |||||||
chr2:163680983 | A | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(92): Show |
96 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.25+53920T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163680983 | |||||||
chr2:163681201 | T | G | 4 | a0001c0001t0030g0096 a0001c0002t0007g0135 a0001c0002t0007g0136 others(1): Show |
4 | HG03225.hp1 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+53702A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681201 | |||||||
chr2:163681273 | A | AAAT | 6 | a0001c0001t0001g0139 a0001c0001t0003g0162 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+53629_25+53630i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681273 | |||||||
chr2:163681389 | T | G | 1 | a0001c0001t0065g0156 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.25+53514A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681389 | |||||||
chr2:163681454 | T | C | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+53449A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681454 | |||||||
chr2:163681521 | G | C | 2 | a0001c0001t0015g0126 a0001c0001t0030g0127 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.25+53382C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681521 | |||||||
chr2:163681542 | C | T | 44 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(41): Show |
44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+53361G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681542 | |||||||
chr2:163681556 | AAAGTGAC others(5): Show |
A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0082 others(2): Show |
5 | HG00741.hp1 HG01106.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+53335_25+53346d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681556 | |||||||
chr2:163681603 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+53300C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681603 | |||||||
chr2:163681632 | G | A | 1 | a0001c0001t0076g0068 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.25+53271C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163681632 | |||||||
chr2:163682192 | C | G | 44 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(41): Show |
44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+52711G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682192 | |||||||
chr2:163682309 | T | C | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+52594A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682309 | |||||||
chr2:163682361 | C | T | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+52542G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682361 | |||||||
chr2:163682372 | C | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+52531G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682372 | |||||||
chr2:163682394 | CACA | C | 115 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0137 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.25+52506_25+52508d others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682394 | |||||||
chr2:163682423 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
83 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.25+52480A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682423 | |||||||
chr2:163682461 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.25+52442C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682461 | |||||||
chr2:163682528 | C | G | 115 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0137 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.25+52375G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682528 | |||||||
chr2:163682773 | C | T | 1 | a0001c0001t0077g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.25+52130G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163682773 | |||||||
chr2:163683067 | G | A | 23 | a0001c0001t0001g0137 a0001c0001t0012g0122 a0001c0001t0019g0254 others(20): Show |
23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+51836C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683067 | |||||||
chr2:163683179 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0006g0062 |
2 | HG00735.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.25+51724C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683179 | |||||||
chr2:163683186 | A | G | 1 | a0001c0002t0028g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+51717T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683186 | |||||||
chr2:163683463 | A | C | 2 | a0001c0001t0070g0103 a0001c0002t0007g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+51440T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683463 | |||||||
chr2:163683814 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.25+51089G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163683814 | |||||||
chr2:163684166 | T | TAC | 22 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0106 others(19): Show |
22 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+50735_25+50736d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684166 | |||||||
chr2:163684257 | C | G | 1 | a0001c0001t0001g0021 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.25+50646G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684257 | |||||||
chr2:163684608 | A | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+50295T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684608 | |||||||
chr2:163684743 | C | T | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+50160G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684743 | |||||||
chr2:163684895 | C | A | 3 | a0001c0001t0001g0098 a0001c0001t0070g0103 a0001c0002t0007g0104 |
3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+50008G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684895 | |||||||
chr2:163684939 | A | AT | 23 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0002g0019 others(20): Show |
23 | HG01496.hp2 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+49963dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684939 | |||||||
chr2:163684939 | AT | A | 22 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0200 others(19): Show |
22 | HG01070.hp1 HG01071.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.25+49963delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684939 | |||||||
chr2:163684939 | ATTTTTT | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0139 a0001c0001t0001g0140 others(30): Show |
33 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.25+49958_25+49963d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163684939 | |||||||
chr2:163685075 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.25+49828C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685075 | |||||||
chr2:163685115 | G | T | 2 | a0001c0001t0034g0250 a0001c0001t0080g0264 |
2 | NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.25+49788C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685115 | |||||||
chr2:163685752 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+49151C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685752 | |||||||
chr2:163685755 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+49148A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685755 | |||||||
chr2:163685851 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+49052T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685851 | |||||||
chr2:163685982 | A | G | 34 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(31): Show |
34 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.25+48921T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163685982 | |||||||
chr2:163686298 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+48605G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686298 | |||||||
chr2:163686385 | T | G | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+48518A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686385 | |||||||
chr2:163686438 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0003g0105 |
2 | HG02818.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.25+48465T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686438 | |||||||
chr2:163686479 | T | C | 89 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0139 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.25+48424A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686479 | |||||||
chr2:163686526 | A | C | 34 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(31): Show |
34 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.25+48377T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686526 | |||||||
chr2:163686660 | A | T | 90 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0139 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.25+48243T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686660 | |||||||
chr2:163686737 | C | A | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+48166G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686737 | |||||||
chr2:163686758 | G | GTA | 25 | a0001c0001t0001g0137 a0001c0001t0003g0116 a0001c0001t0005g0117 others(22): Show |
25 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.25+48143_25+48144d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686758 | |||||||
chr2:163686760 | A | G | 1 | a0001c0001t0004g0034 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.25+48143T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686760 | |||||||
chr2:163686777 | T | TAC | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
104 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.25+48124_25+48125d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686777 | |||||||
chr2:163686777 | T | TACAC | 20 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0002g0038 others(17): Show |
20 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.25+48122_25+48125d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686777 | |||||||
chr2:163686795 | CATAT | C | 4 | a0001c0001t0025g0109 a0001c0001t0027g0107 a0001c0001t0045g0177 others(1): Show |
4 | HG02723.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+48104_25+48107d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686795 | |||||||
chr2:163686797 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0043 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.25+48106A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686797 | |||||||
chr2:163686799 | T | C | 109 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0137 others(106): Show |
109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.25+48104A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686799 | |||||||
chr2:163686828 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+48075A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686828 | |||||||
chr2:163686953 | T | C | 19 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0116 others(16): Show |
19 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+47950A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163686953 | |||||||
chr2:163687012 | T | TAC | 6 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
6 | HG02280.hp1 HG02698.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+47889_25+47890d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687012 | |||||||
chr2:163687012 | TAC | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0140 a0001c0001t0001g0163 others(9): Show |
12 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+47889_25+47890d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687012 | |||||||
chr2:163687168 | A | C | 1 | a0002c0005t0054g0017 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25+47735T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687168 | |||||||
chr2:163687187 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.25+47716G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687187 | |||||||
chr2:163687599 | T | C | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+47304A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687599 | |||||||
chr2:163687996 | T | C | 3 | a0001c0002t0007g0135 a0001c0002t0007g0136 a0001c0002t0028g0134 |
3 | HG03225.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.25+46907A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163687996 | |||||||
chr2:163688000 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+46903G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688000 | |||||||
chr2:163688117 | A | G | 11 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+46786T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688117 | |||||||
chr2:163688173 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.25+46730C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688173 | |||||||
chr2:163688200 | G | C | 20 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0116 others(17): Show |
20 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.25+46703C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688200 | |||||||
chr2:163688250 | A | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0140 a0001c0001t0001g0141 others(18): Show |
21 | HG00140.hp1 HG00558.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+46653T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688250 | |||||||
chr2:163688572 | A | G | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+46331T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688572 | |||||||
chr2:163688817 | C | T | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+46086G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688817 | |||||||
chr2:163688892 | G | T | 1 | a0001c0001t0042g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.25+46011C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163688892 | |||||||
chr2:163689173 | A | AACACAC | 2 | a0001c0001t0003g0097 a0001c0001t0003g0105 |
2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.25+45724_25+45729d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(1): Show |
8 | a0001c0001t0005g0033 a0001c0001t0005g0174 a0001c0001t0030g0096 others(5): Show |
8 | HG00408.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+45722_25+45729d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(3): Show |
23 | a0001c0001t0002g0051 a0001c0001t0003g0102 a0001c0001t0003g0193 others(20): Show |
23 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+45720_25+45729d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(5): Show |
21 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0115 others(18): Show |
21 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+45718_25+45729d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(7): Show |
78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
78 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.25+45716_25+45729d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(9): Show |
50 | a0001c0001t0001g0016 a0001c0001t0001g0055 a0001c0001t0001g0118 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.25+45714_25+45729d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(11): Show |
66 | a0001c0001t0001g0043 a0001c0001t0001g0077 a0001c0001t0001g0119 others(63): Show |
67 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.25+45712_25+45729d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(13): Show |
9 | a0001c0001t0001g0202 a0001c0001t0002g0229 a0001c0001t0004g0225 others(6): Show |
9 | HG00408.hp2 HG02129.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+45710_25+45729d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(15): Show |
2 | a0001c0001t0002g0233 a0001c0001t0045g0177 |
2 | HG02015.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.25+45708_25+45729d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689173 | A | AACACACA others(25): Show |
1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+45729_25+45730i others(34): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689173 | |||||||
chr2:163689274 | A | T | 1 | a0001c0001t0081g0257 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+45629T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689274 | |||||||
chr2:163689426 | A | G | 12 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+45477T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689426 | |||||||
chr2:163689451 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+45452A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689451 | |||||||
chr2:163689687 | T | G | 119 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0119 others(116): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.25+45216A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689687 | |||||||
chr2:163689996 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+44907A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163689996 | |||||||
chr2:163690180 | T | C | 3 | a0001c0001t0021g0184 a0001c0001t0050g0172 a0001c0002t0013g0191 |
3 | HG02559.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.25+44723A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690180 | |||||||
chr2:163690377 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0014g0025 |
2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.25+44526T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690377 | |||||||
chr2:163690408 | G | A | 11 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+44495C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690408 | |||||||
chr2:163690432 | C | T | 5 | a0001c0001t0031g0131 a0001c0002t0007g0135 a0001c0002t0007g0136 others(2): Show |
5 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+44471G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690432 | |||||||
chr2:163690562 | T | C | 1 | a0001c0001t0006g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.25+44341A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690562 | |||||||
chr2:163690583 | CAGTCT | C | 4 | a0001c0001t0002g0035 a0001c0001t0002g0050 a0001c0001t0004g0034 others(1): Show |
4 | HG02155.hp2 NA18977.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+44315_25+44319d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690583 | |||||||
chr2:163690588 | T | C | 35 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(32): Show |
35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+44315A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690588 | |||||||
chr2:163690802 | C | CAAAAATG others(1): Show |
22 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0106 others(19): Show |
22 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+44093_25+44100d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690802 | |||||||
chr2:163690830 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+44073G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690830 | |||||||
chr2:163690919 | A | C | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25+43984T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690919 | |||||||
chr2:163690930 | T | C | 24 | a0001c0001t0001g0137 a0001c0001t0012g0122 a0001c0001t0019g0254 others(21): Show |
24 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+43973A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163690930 | |||||||
chr2:163691088 | C | T | 1 | a0001c0001t0006g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.25+43815G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691088 | |||||||
chr2:163691281 | C | T | 4 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0023g0157 others(1): Show |
4 | HG00558.hp1 HG01496.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+43622G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691281 | |||||||
chr2:163691490 | T | C | 1 | a0001c0001t0012g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+43413A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691490 | |||||||
chr2:163691614 | G | A | 6 | a0001c0001t0002g0038 a0001c0001t0004g0036 a0001c0001t0004g0037 others(3): Show |
6 | HG02015.hp2 NA18943.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+43289C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691614 | |||||||
chr2:163691689 | A | G | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+43214T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691689 | |||||||
chr2:163691693 | A | G | 3 | a0001c0001t0005g0174 a0001c0004t0033g0138 a0001c0004t0033g0175 |
3 | HG01070.hp1 HG01071.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.25+43210T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691693 | |||||||
chr2:163691766 | TA | T | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+43136delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691766 | |||||||
chr2:163691799 | G | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+43104C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691799 | |||||||
chr2:163691867 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0140 a0001c0001t0001g0163 others(1): Show |
4 | HG00140.hp1 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+43036C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163691867 | |||||||
chr2:163692219 | T | C | 2 | a0001c0001t0003g0106 a0001c0001t0004g0190 |
2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+42684A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692219 | |||||||
chr2:163692230 | T | G | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+42673A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692230 | |||||||
chr2:163692324 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25+42579T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692324 | |||||||
chr2:163692400 | G | A | 1 | a0001c0001t0014g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.25+42503C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692400 | |||||||
chr2:163692719 | T | A | 1 | a0001c0001t0045g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.25+42184A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692719 | |||||||
chr2:163692740 | C | T | 2 | a0001c0001t0048g0209 a0001c0003t0002g0204 |
2 | NA18973.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.25+42163G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163692740 | |||||||
chr2:163693009 | G | A | 1 | a0001c0001t0008g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.25+41894C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693009 | |||||||
chr2:163693103 | G | T | 1 | a0001c0001t0023g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.25+41800C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693103 | |||||||
chr2:163693115 | C | T | 1 | a0001c0001t0047g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.25+41788G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693115 | |||||||
chr2:163693243 | C | T | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+41660G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693243 | |||||||
chr2:163693291 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.25+41612C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693291 | |||||||
chr2:163693388 | C | T | 7 | a0001c0001t0004g0133 a0001c0001t0030g0096 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+41515G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693388 | |||||||
chr2:163693582 | G | A | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+41321C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693582 | |||||||
chr2:163693693 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+41210A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693693 | |||||||
chr2:163693811 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.25+41092G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693811 | |||||||
chr2:163693968 | G | T | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+40935C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163693968 | |||||||
chr2:163694001 | T | C | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+40902A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694001 | |||||||
chr2:163694131 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(111): Show |
115 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.25+40772T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694131 | |||||||
chr2:163694365 | T | A | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+40538A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694365 | |||||||
chr2:163694460 | C | T | 23 | a0001c0001t0001g0137 a0001c0001t0012g0122 a0001c0001t0019g0254 others(20): Show |
23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+40443G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694460 | |||||||
chr2:163694475 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.25+40428C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694475 | |||||||
chr2:163694639 | C | T | 35 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(32): Show |
35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+40264G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694639 | |||||||
chr2:163694699 | T | G | 1 | a0001c0001t0004g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.25+40204A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694699 | |||||||
chr2:163694868 | G | C | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+40035C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163694868 | |||||||
chr2:163695020 | T | G | 1 | a0001c0002t0007g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.25+39883A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695020 | |||||||
chr2:163695070 | GTC | G | 111 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0137 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.25+39831_25+39832d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695070 | |||||||
chr2:163695225 | C | A | 33 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(30): Show |
33 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.25+39678G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695225 | |||||||
chr2:163695583 | C | T | 1 | a0001c0001t0078g0057 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+39320G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695583 | |||||||
chr2:163695593 | C | A | 1 | a0001c0002t0007g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.25+39310G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695593 | |||||||
chr2:163695749 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+39154C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695749 | |||||||
chr2:163695845 | C | G | 1 | a0001c0001t0012g0024 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.25+39058G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163695845 | |||||||
chr2:163696171 | T | C | 35 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0176 others(32): Show |
35 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+38732A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696171 | |||||||
chr2:163696283 | T | C | 11 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+38620A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696283 | |||||||
chr2:163696364 | GA | G | 6 | a0001c0001t0001g0139 a0001c0001t0003g0162 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+38538delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696364 | |||||||
chr2:163696377 | G | C | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
7 | NA18747.hp1 NA18941.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+38526C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696377 | |||||||
chr2:163696433 | A | T | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+38470T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696433 | |||||||
chr2:163696732 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+38171C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696732 | |||||||
chr2:163696834 | A | AT | 7 | a0001c0001t0001g0236 a0001c0001t0003g0193 a0001c0001t0004g0192 others(4): Show |
7 | HG02647.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+38068dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696834 | |||||||
chr2:163696834 | AT | A | 38 | a0001c0001t0001g0041 a0001c0001t0001g0098 a0001c0001t0001g0176 others(35): Show |
38 | HG00558.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.25+38068delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163696834 | |||||||
chr2:163697026 | C | T | 11 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+37877G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697026 | |||||||
chr2:163697027 | G | A | 7 | a0001c0001t0004g0133 a0001c0001t0030g0096 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+37876C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697027 | |||||||
chr2:163697100 | C | CT | 26 | a0001c0001t0001g0115 a0001c0001t0003g0097 a0001c0001t0003g0102 others(23): Show |
26 | HG00558.hp1 HG00735.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.25+37802dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697100 | |||||||
chr2:163697100 | C | CTT | 4 | a0001c0001t0031g0091 a0001c0001t0059g0093 a0001c0002t0007g0244 others(1): Show |
4 | HG01175.hp1 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+37801_25+37802d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697100 | |||||||
chr2:163697100 | CTTTCTTT others(5): Show |
C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0066g0039 |
3 | NA19004.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.25+37791_25+37802d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697100 | |||||||
chr2:163697102 | TTC | T | 10 | a0001c0001t0001g0139 a0001c0001t0002g0146 a0001c0001t0004g0226 others(7): Show |
10 | HG01070.hp2 HG01496.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+37799_25+37800d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697102 | |||||||
chr2:163697103 | TC | T | 109 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(106): Show |
109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.25+37799delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697103 | |||||||
chr2:163697104 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(135): Show |
139 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.25+37799G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697104 | |||||||
chr2:163697105 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+37798A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697105 | |||||||
chr2:163697194 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(87): Show |
91 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.25+37709C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697194 | |||||||
chr2:163697218 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+37685T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697218 | |||||||
chr2:163697220 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+37683G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697220 | |||||||
chr2:163697274 | T | C | 1 | a0001c0001t0067g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.25+37629A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697274 | |||||||
chr2:163697293 | G | A | 7 | a0001c0001t0004g0133 a0001c0001t0030g0096 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+37610C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697293 | |||||||
chr2:163697348 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+37555C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697348 | |||||||
chr2:163697441 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+37462C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697441 | |||||||
chr2:163697470 | GC | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0140 a0001c0001t0001g0163 others(1): Show |
4 | HG00140.hp1 HG03239.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+37432delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697470 | |||||||
chr2:163697489 | G | A | 7 | a0001c0001t0004g0133 a0001c0001t0030g0096 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+37414C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697489 | |||||||
chr2:163697668 | C | A | 2 | a0001c0001t0031g0091 a0001c0001t0059g0093 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.25+37235G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697668 | |||||||
chr2:163697738 | C | T | 4 | a0001c0001t0025g0109 a0001c0001t0027g0107 a0001c0001t0045g0177 others(1): Show |
4 | HG02723.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+37165G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697738 | |||||||
chr2:163697818 | T | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0139 a0001c0001t0001g0140 others(31): Show |
34 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.25+37085A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163697818 | |||||||
chr2:163698023 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+36880G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698023 | |||||||
chr2:163698363 | T | C | 1 | a0001c0001t0027g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.25+36540A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698363 | |||||||
chr2:163698464 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+36439G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698464 | |||||||
chr2:163698501 | T | A | 11 | a0001c0001t0001g0098 a0001c0001t0001g0176 a0001c0001t0003g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+36402A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698501 | |||||||
chr2:163698696 | G | C | 1 | a0001c0001t0075g0009 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.25+36207C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698696 | |||||||
chr2:163698718 | G | A | 1 | a0001c0001t0059g0093 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.25+36185C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698718 | |||||||
chr2:163698881 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0070g0103 a0001c0002t0007g0104 |
3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+36022C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698881 | |||||||
chr2:163698930 | T | C | 44 | a0001c0001t0001g0043 a0001c0001t0001g0196 a0001c0001t0001g0199 others(41): Show |
44 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+35973A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163698930 | |||||||
chr2:163699244 | A | G | 1 | a0001c0001t0016g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.25+35659T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699244 | |||||||
chr2:163699258 | G | C | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+35645C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699258 | |||||||
chr2:163699287 | A | AT | 4 | a0001c0001t0005g0174 a0001c0001t0006g0023 a0001c0004t0033g0138 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+35615dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699287 | |||||||
chr2:163699456 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25+35447A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699456 | |||||||
chr2:163699465 | T | C | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+35438A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699465 | |||||||
chr2:163699510 | T | TGTACTGG others(2): Show |
226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(223): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.25+35392_25+35393i others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699510 | |||||||
chr2:163699568 | C | A | 1 | a0001c0001t0012g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+35335G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699568 | |||||||
chr2:163699988 | A | C | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.25+34915T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163699988 | |||||||
chr2:163700059 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+34844C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700059 | |||||||
chr2:163700072 | A | G | 1 | a0001c0001t0009g0197 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.25+34831T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700072 | |||||||
chr2:163700074 | G | A | 1 | a0001c0001t0009g0197 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.25+34829C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700074 | |||||||
chr2:163700095 | C | G | 5 | a0001c0001t0001g0119 a0001c0001t0016g0130 a0001c0001t0024g0001 others(2): Show |
6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+34808G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700095 | |||||||
chr2:163700160 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+34743A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700160 | |||||||
chr2:163700197 | T | G | 1 | a0001c0001t0050g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+34706A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700197 | |||||||
chr2:163700280 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0005g0080 |
2 | HG01261.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.25+34623T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700280 | |||||||
chr2:163700409 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.25+34494C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700409 | |||||||
chr2:163700446 | G | A | 1 | a0001c0001t0022g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.25+34457C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700446 | |||||||
chr2:163700553 | T | C | 1 | a0001c0001t0006g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.25+34350A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700553 | |||||||
chr2:163700663 | T | C | 1 | a0001c0002t0028g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+34240A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700663 | |||||||
chr2:163700826 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.25+34077C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700826 | |||||||
chr2:163700833 | G | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+34070C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700833 | |||||||
chr2:163700950 | C | T | 23 | a0001c0001t0001g0137 a0001c0001t0012g0122 a0001c0001t0019g0254 others(20): Show |
23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+33953G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163700950 | |||||||
chr2:163701013 | A | G | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+33890T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701013 | |||||||
chr2:163701074 | A | G | 13 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0004g0133 others(10): Show |
13 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.25+33829T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701074 | |||||||
chr2:163701471 | C | T | 4 | a0001c0001t0003g0097 a0001c0001t0031g0091 a0001c0001t0059g0093 others(1): Show |
4 | HG02559.hp1 HG02886.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+33432G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701471 | |||||||
chr2:163701493 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.25+33410G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701493 | |||||||
chr2:163701658 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+33245T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701658 | |||||||
chr2:163701713 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+33190G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701713 | |||||||
chr2:163701801 | C | A | 4 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0089 others(1): Show |
4 | HG02074.hp2 NA18946.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+33102G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701801 | |||||||
chr2:163701852 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+33051G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701852 | |||||||
chr2:163701919 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
85 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.25+32984T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163701919 | |||||||
chr2:163702280 | G | A | 1 | a0001c0001t0071g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.25+32623C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702280 | |||||||
chr2:163702350 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.25+32553G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702350 | |||||||
chr2:163702426 | C | T | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+32477G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702426 | |||||||
chr2:163702719 | C | A | 3 | a0001c0001t0002g0229 a0001c0001t0022g0216 a0001c0001t0052g0218 |
3 | HG00408.hp2 HG02135.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.25+32184G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702719 | |||||||
chr2:163702741 | C | T | 1 | a0001c0009t0005g0237 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.25+32162G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702741 | |||||||
chr2:163702822 | C | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(88): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.25+32081G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702822 | |||||||
chr2:163702961 | G | A | 18 | a0001c0001t0003g0097 a0001c0001t0003g0102 a0001c0001t0003g0240 others(15): Show |
18 | HG00558.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+31942C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163702961 | |||||||
chr2:163703030 | C | CT | 7 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0006g0239 others(4): Show |
7 | HG02109.hp1 HG02135.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+31872dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703030 | |||||||
chr2:163703115 | A | G | 1 | a0001c0001t0010g0052 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.25+31788T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703115 | |||||||
chr2:163703123 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.25+31780A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703123 | |||||||
chr2:163703196 | T | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+31707A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703196 | |||||||
chr2:163703455 | C | A | 7 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(4): Show |
7 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+31448G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703455 | |||||||
chr2:163703479 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0070g0103 a0001c0002t0007g0104 |
3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+31424G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703479 | |||||||
chr2:163703702 | A | G | 1 | a0001c0001t0032g0014 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.25+31201T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703702 | |||||||
chr2:163703801 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.25+31102C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163703801 | |||||||
chr2:163704029 | G | A | 2 | a0001c0001t0021g0243 a0001c0002t0007g0242 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.25+30874C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704029 | |||||||
chr2:163704185 | G | A | 1 | a0001c0001t0056g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25+30718C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704185 | |||||||
chr2:163704370 | T | C | 16 | a0001c0001t0001g0115 a0001c0001t0003g0106 a0001c0001t0003g0187 others(13): Show |
16 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+30533A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704370 | |||||||
chr2:163704370 | T | G | 3 | a0001c0001t0025g0109 a0001c0001t0027g0107 a0001c0001t0057g0108 |
3 | HG03139.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.25+30533A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704370 | |||||||
chr2:163704503 | T | C | 10 | a0001c0001t0001g0115 a0001c0001t0003g0106 a0001c0001t0003g0187 others(7): Show |
10 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+30400A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704503 | |||||||
chr2:163704615 | G | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(247): Show |
251 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.25+30288C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704615 | |||||||
chr2:163704625 | T | TCTCTCTC others(4): Show |
3 | a0001c0001t0001g0028 a0001c0001t0004g0190 a0002c0005t0054g0017 |
3 | HG00639.hp2 HG03130.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.25+30277_25+30278i others(13): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TCTCTCTC others(6): Show |
2 | a0001c0001t0001g0046 a0001c0001t0006g0023 |
2 | NA18991.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.25+30277_25+30278i others(15): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TCTCTCTC others(8): Show |
1 | a0001c0001t0002g0026 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.25+30277_25+30278i others(17): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TCTCTCTC others(10): Show |
1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+30277_25+30278i others(19): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TCTCTCTC others(12): Show |
4 | a0001c0001t0001g0219 a0001c0001t0005g0174 a0001c0002t0007g0104 others(1): Show |
4 | HG01071.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+30277_25+30278i others(21): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TCTCTCTC others(14): Show |
2 | a0001c0001t0003g0102 a0001c0002t0003g0100 |
2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.25+30277_25+30278i others(23): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTC | 28 | a0001c0001t0001g0021 a0001c0001t0001g0140 a0001c0001t0001g0152 others(25): Show |
28 | HG00558.hp1 HG01358.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.25+30276_25+30277d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTC | 16 | a0001c0001t0001g0110 a0001c0001t0001g0141 a0001c0001t0001g0158 others(13): Show |
16 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.25+30274_25+30277d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTC | 3 | a0001c0001t0001g0143 a0001c0001t0002g0144 a0001c0001t0043g0210 |
3 | NA18945.hp2 NA18969.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.25+30272_25+30277d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(1): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0079 others(11): Show |
14 | HG01106.hp2 HG01167.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.25+30270_25+30277d others(10): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(3): Show |
21 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0056 others(18): Show |
21 | HG00323.hp2 HG01255.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+30268_25+30277d others(12): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(5): Show |
27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0016 others(24): Show |
27 | HG00423.hp1 HG01071.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.25+30266_25+30277d others(14): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(7): Show |
44 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0047 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+30264_25+30277d others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(9): Show |
15 | a0001c0001t0001g0078 a0001c0001t0002g0038 a0001c0001t0002g0050 others(12): Show |
15 | HG02015.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+30262_25+30277d others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(11): Show |
13 | a0001c0001t0001g0098 a0001c0001t0001g0220 a0001c0001t0001g0236 others(10): Show |
13 | HG00408.hp2 HG01891.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.25+30260_25+30277d others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(13): Show |
5 | a0001c0001t0004g0226 a0001c0001t0006g0099 a0001c0001t0006g0235 others(2): Show |
5 | HG01070.hp1 HG02055.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+30258_25+30277d others(22): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(15): Show |
5 | a0001c0001t0003g0087 a0001c0001t0003g0116 a0001c0001t0005g0117 others(2): Show |
5 | HG02132.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+30256_25+30277d others(24): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(17): Show |
4 | a0001c0001t0001g0055 a0001c0001t0003g0070 a0001c0001t0004g0225 others(1): Show |
4 | HG02135.hp1 HG03139.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+30254_25+30277d others(26): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704625 | T | TTCTCTCT others(19): Show |
1 | a0001c0001t0013g0101 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25+30252_25+30277d others(28): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704625 | |||||||
chr2:163704656 | T | TCTCTCTC others(7): Show |
3 | a0001c0001t0002g0203 a0001c0001t0003g0106 a0001c0003t0002g0204 |
3 | NA18973.hp2 NA18977.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+30246_25+30247i others(16): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | |||||||
chr2:163704656 | T | TCTCTCTC others(9): Show |
1 | a0001c0001t0001g0199 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.25+30246_25+30247i others(18): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | |||||||
chr2:163704656 | TCA | T | 15 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(12): Show |
15 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+30245_25+30246d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | |||||||
chr2:163704656 | TCACA | T | 8 | a0001c0001t0015g0126 a0001c0001t0016g0130 a0001c0001t0023g0166 others(5): Show |
8 | HG01261.hp1 HG01515.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+30243_25+30246d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | |||||||
chr2:163704656 | TCACACA | T | 4 | a0001c0001t0001g0119 a0001c0001t0024g0001 a0001c0001t0056g0121 others(1): Show |
5 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+30241_25+30246d others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704656 | |||||||
chr2:163704658 | A | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.25+30245T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704658 | |||||||
chr2:163704660 | A | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.25+30243T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704660 | |||||||
chr2:163704662 | A | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0137 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.25+30241T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704662 | |||||||
chr2:163704664 | A | T | 17 | a0001c0001t0019g0254 a0001c0001t0020g0247 a0001c0001t0020g0256 others(14): Show |
17 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.25+30239T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704664 | |||||||
chr2:163704798 | G | T | 23 | a0001c0001t0001g0118 a0001c0001t0001g0137 a0001c0001t0019g0254 others(20): Show |
23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+30105C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163704798 | |||||||
chr2:163705049 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+29854A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705049 | |||||||
chr2:163705300 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.25+29603G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705300 | |||||||
chr2:163705417 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.25+29486A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705417 | |||||||
chr2:163705478 | A | T | 9 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+29425T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705478 | |||||||
chr2:163705607 | T | A | 1 | a0001c0003t0032g0086 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.25+29296A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705607 | |||||||
chr2:163705830 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+29073T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705830 | |||||||
chr2:163705904 | A | C | 1 | a0001c0003t0068g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.25+28999T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705904 | |||||||
chr2:163705904 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.25+28999T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705904 | |||||||
chr2:163705985 | G | T | 1 | a0001c0002t0004g0185 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+28918C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163705985 | |||||||
chr2:163706106 | T | A | 3 | a0001c0001t0003g0106 a0001c0001t0004g0190 a0001c0002t0004g0185 |
3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+28797A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706106 | |||||||
chr2:163706156 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+28747T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706156 | |||||||
chr2:163706189 | A | G | 12 | a0001c0001t0001g0115 a0001c0001t0003g0106 a0001c0001t0003g0187 others(9): Show |
12 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+28714T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706189 | |||||||
chr2:163706279 | G | A | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25+28624C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706279 | |||||||
chr2:163706624 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(247): Show |
251 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.25+28279T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706624 | |||||||
chr2:163706761 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+28142A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706761 | |||||||
chr2:163706914 | C | T | 3 | a0001c0001t0025g0109 a0001c0001t0027g0107 a0001c0001t0057g0108 |
3 | HG03139.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.25+27989G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163706914 | |||||||
chr2:163707174 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.25+27729G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707174 | |||||||
chr2:163707184 | CA | C | 4 | a0001c0001t0020g0263 a0001c0001t0036g0245 a0001c0001t0084g0253 others(1): Show |
4 | NA18944.hp1 NA18961.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+27718delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707184 | |||||||
chr2:163707354 | CA | C | 12 | a0001c0001t0001g0152 a0001c0001t0001g0176 a0001c0001t0002g0050 others(9): Show |
12 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+27548delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707354 | |||||||
chr2:163707354 | CAA | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(244): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.25+27547_25+27548d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707354 | |||||||
chr2:163707419 | G | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(247): Show |
251 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.25+27484C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163707419 | |||||||
chr2:163708056 | T | C | 1 | a0001c0001t0006g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+26847A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708056 | |||||||
chr2:163708258 | C | A | 11 | a0001c0001t0003g0193 a0001c0001t0004g0133 a0001c0001t0004g0192 others(8): Show |
11 | HG02280.hp2 HG02809.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+26645G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708258 | |||||||
chr2:163708271 | CTTAA | C | 23 | a0001c0001t0001g0118 a0001c0001t0001g0137 a0001c0001t0019g0254 others(20): Show |
23 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25+26628_25+26631d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708271 | |||||||
chr2:163708322 | T | C | 1 | a0001c0001t0020g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.25+26581A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708322 | |||||||
chr2:163708453 | T | C | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+26450A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708453 | |||||||
chr2:163708636 | T | C | 1 | a0001c0001t0063g0234 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.25+26267A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708636 | |||||||
chr2:163708650 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+26253A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708650 | |||||||
chr2:163708734 | G | A | 1 | a0002c0005t0054g0017 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25+26169C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708734 | |||||||
chr2:163708853 | G | A | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+26050C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708853 | |||||||
chr2:163708905 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+25998C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163708905 | |||||||
chr2:163709018 | G | A | 3 | a0001c0001t0021g0184 a0001c0001t0030g0096 a0001c0002t0013g0191 |
3 | HG03098.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.25+25885C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709018 | |||||||
chr2:163709025 | C | T | 2 | a0001c0001t0009g0128 a0001c0002t0011g0129 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+25878G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709025 | |||||||
chr2:163709124 | C | T | 22 | a0001c0001t0001g0137 a0001c0001t0019g0254 a0001c0001t0019g0261 others(19): Show |
22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+25779G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709124 | |||||||
chr2:163709133 | C | G | 5 | a0001c0001t0001g0119 a0001c0001t0016g0130 a0001c0001t0024g0001 others(2): Show |
6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+25770G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709133 | |||||||
chr2:163709154 | C | T | 1 | a0001c0001t0050g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+25749G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709154 | |||||||
chr2:163709346 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.25+25557A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709346 | |||||||
chr2:163709461 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0010g0052 |
2 | HG02129.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.25+25442C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709461 | |||||||
chr2:163709650 | C | T | 1 | a0001c0001t0083g0251 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.25+25253G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709650 | |||||||
chr2:163709713 | A | G | 5 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0159 others(2): Show |
5 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+25190T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709713 | |||||||
chr2:163709784 | GA | G | 5 | a0001c0001t0031g0131 a0001c0002t0007g0135 a0001c0002t0007g0136 others(2): Show |
5 | HG02280.hp2 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+25118delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709784 | |||||||
chr2:163709797 | T | C | 1 | a0001c0001t0010g0052 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.25+25106A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709797 | |||||||
chr2:163709898 | A | G | 1 | a0001c0001t0045g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.25+25005T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163709898 | |||||||
chr2:163710276 | G | A | 2 | a0001c0001t0003g0162 a0001c0001t0072g0161 |
2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.25+24627C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710276 | |||||||
chr2:163710332 | C | G | 84 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.25+24571G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710332 | |||||||
chr2:163710354 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.25+24549A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710354 | |||||||
chr2:163710374 | C | T | 4 | a0001c0001t0003g0070 a0001c0001t0003g0087 a0001c0001t0007g0020 others(1): Show |
4 | HG02055.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+24529G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710374 | |||||||
chr2:163710905 | C | T | 1 | a0001c0001t0002g0019 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.25+23998G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163710905 | |||||||
chr2:163711129 | C | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+23774G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711129 | |||||||
chr2:163711151 | G | T | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.25+23752C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711151 | |||||||
chr2:163711171 | G | A | 1 | a0001c0001t0005g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.25+23732C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711171 | |||||||
chr2:163711179 | T | C | 84 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.25+23724A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711179 | |||||||
chr2:163711316 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.25+23587C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711316 | |||||||
chr2:163711393 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+23510C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711393 | |||||||
chr2:163711524 | G | A | 3 | a0001c0001t0003g0106 a0001c0001t0004g0190 a0001c0002t0004g0185 |
3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+23379C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711524 | |||||||
chr2:163711657 | C | CA | 196 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(193): Show |
197 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.25+23245dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711657 | |||||||
chr2:163711657 | C | CAA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0056 others(16): Show |
19 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+23244_25+23245d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711657 | |||||||
chr2:163711791 | C | T | 1 | a0002c0005t0054g0017 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.25+23112G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711791 | |||||||
chr2:163711865 | C | G | 3 | a0001c0001t0003g0106 a0001c0001t0004g0190 a0001c0002t0004g0185 |
3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+23038G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711865 | |||||||
chr2:163711939 | C | T | 1 | a0001c0001t0031g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.25+22964G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163711939 | |||||||
chr2:163712016 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.25+22887G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712016 | |||||||
chr2:163712071 | G | A | 1 | a0001c0002t0028g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+22832C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712071 | |||||||
chr2:163712280 | GA | G | 3 | a0001c0001t0001g0098 a0001c0001t0070g0103 a0001c0002t0007g0104 |
3 | HG02809.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.25+22622delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712280 | |||||||
chr2:163712580 | C | T | 1 | a0001c0001t0045g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.25+22323G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712580 | |||||||
chr2:163712819 | G | C | 1 | a0001c0001t0021g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25+22084C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163712819 | |||||||
chr2:163713027 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+21876T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713027 | |||||||
chr2:163713130 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+21773A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713130 | |||||||
chr2:163713242 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+21661T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713242 | |||||||
chr2:163713448 | C | CCA | 8 | a0001c0001t0002g0058 a0001c0001t0002g0088 a0001c0001t0003g0105 others(5): Show |
8 | HG02040.hp1 HG02040.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+21453_25+21454d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713448 | |||||||
chr2:163713448 | CCA | C | 9 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+21453_25+21454d others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713448 | |||||||
chr2:163713483 | G | A | 43 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0200 others(40): Show |
43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+21420C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713483 | |||||||
chr2:163713515 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25+21388C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713515 | |||||||
chr2:163713524 | C | T | 9 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+21379G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713524 | |||||||
chr2:163713702 | C | T | 1 | a0001c0001t0015g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.25+21201G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713702 | |||||||
chr2:163713890 | C | T | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+21013G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713890 | |||||||
chr2:163713923 | G | A | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+20980C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163713923 | |||||||
chr2:163714018 | G | C | 8 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(5): Show |
8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+20885C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714018 | |||||||
chr2:163714235 | C | A | 22 | a0001c0001t0001g0137 a0001c0001t0019g0254 a0001c0001t0019g0261 others(19): Show |
22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+20668G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714235 | |||||||
chr2:163714303 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(245): Show |
249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.25+20600G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714303 | |||||||
chr2:163714453 | C | G | 4 | a0001c0001t0008g0168 a0001c0001t0008g0181 a0001c0001t0023g0157 others(1): Show |
4 | HG00558.hp1 HG01496.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+20450G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714453 | |||||||
chr2:163714488 | A | G | 2 | a0001c0001t0015g0126 a0001c0001t0030g0127 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.25+20415T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714488 | |||||||
chr2:163714609 | C | T | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+20294G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714609 | |||||||
chr2:163714780 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25+20123G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714780 | |||||||
chr2:163714984 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+19919G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163714984 | |||||||
chr2:163715111 | C | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+19792G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715111 | |||||||
chr2:163715225 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.25+19678C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715225 | |||||||
chr2:163715861 | T | C | 2 | a0001c0001t0009g0128 a0001c0002t0011g0129 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+19042A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715861 | |||||||
chr2:163715949 | C | T | 9 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+18954G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715949 | |||||||
chr2:163715971 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.25+18932T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163715971 | |||||||
chr2:163716152 | C | T | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+18751G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716152 | |||||||
chr2:163716153 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.25+18750C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716153 | |||||||
chr2:163716154 | T | C | 1 | a0001c0001t0005g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.25+18749A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716154 | |||||||
chr2:163716442 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+18461T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716442 | |||||||
chr2:163716860 | C | T | 1 | a0001c0003t0002g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.25+18043G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163716860 | |||||||
chr2:163717203 | T | C | 2 | a0001c0001t0021g0184 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.25+17700A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717203 | |||||||
chr2:163717306 | A | G | 1 | a0001c0001t0032g0014 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.25+17597T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717306 | |||||||
chr2:163717320 | A | T | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+17583T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717320 | |||||||
chr2:163717337 | C | G | 109 | a0001c0001t0001g0098 a0001c0001t0001g0119 a0001c0001t0001g0139 others(106): Show |
110 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.25+17566G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717337 | |||||||
chr2:163717441 | G | C | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+17462C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717441 | |||||||
chr2:163717506 | T | C | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.25+17397A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717506 | |||||||
chr2:163717512 | G | A | 1 | a0001c0001t0036g0249 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.25+17391C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717512 | |||||||
chr2:163717609 | G | A | 9 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+17294C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717609 | |||||||
chr2:163717760 | C | T | 8 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(5): Show |
8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+17143G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717760 | |||||||
chr2:163717804 | A | G | 1 | a0001c0001t0037g0265 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.25+17099T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717804 | |||||||
chr2:163717834 | T | C | 22 | a0001c0001t0001g0137 a0001c0001t0019g0254 a0001c0001t0019g0261 others(19): Show |
22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+17069A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163717834 | |||||||
chr2:163718392 | T | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0181 |
2 | HG00558.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.25+16511A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718392 | |||||||
chr2:163718457 | C | T | 1 | a0001c0001t0006g0235 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.25+16446G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718457 | |||||||
chr2:163718652 | A | G | 1 | a0001c0001t0004g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25+16251T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718652 | |||||||
chr2:163718783 | G | A | 1 | a0001c0001t0036g0249 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.25+16120C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718783 | |||||||
chr2:163718838 | A | AGC | 115 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0118 others(112): Show |
116 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.25+16064_25+16065i others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718838 | |||||||
chr2:163718840 | T | A | 115 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0118 others(112): Show |
116 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.25+16063A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718840 | |||||||
chr2:163718840 | T | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(119): Show |
122 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.25+16063A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718840 | |||||||
chr2:163718956 | T | C | 8 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(5): Show |
8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+15947A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163718956 | |||||||
chr2:163719006 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+15897T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719006 | |||||||
chr2:163719129 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+15774A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719129 | |||||||
chr2:163719274 | T | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02630.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.25+15629A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719274 | |||||||
chr2:163719581 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+15322C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719581 | |||||||
chr2:163719666 | G | A | 4 | a0001c0001t0002g0064 a0001c0001t0005g0065 a0001c0001t0009g0063 others(1): Show |
4 | HG00423.hp2 NA18994.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+15237C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719666 | |||||||
chr2:163719675 | TG | T | 5 | a0001c0001t0003g0102 a0001c0001t0006g0099 a0001c0001t0013g0101 others(2): Show |
5 | HG02055.hp2 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+15227delC | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719675 | |||||||
chr2:163719774 | C | T | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+15129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719774 | |||||||
chr2:163719821 | T | A | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25+15082A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719821 | |||||||
chr2:163719985 | T | A | 1 | a0001c0001t0023g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.25+14918A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719985 | |||||||
chr2:163719986 | A | T | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+14917T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719986 | |||||||
chr2:163719989 | C | A | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+14914G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163719989 | |||||||
chr2:163720233 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.25+14670G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720233 | |||||||
chr2:163720331 | C | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(87): Show |
90 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.25+14572G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720331 | |||||||
chr2:163720358 | C | T | 2 | a0001c0001t0035g0246 a0001c0008t0035g0248 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.25+14545G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720358 | |||||||
chr2:163720407 | T | C | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25+14496A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720407 | |||||||
chr2:163720616 | G | T | 6 | a0001c0001t0003g0105 a0001c0001t0003g0193 a0001c0001t0004g0192 others(3): Show |
6 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+14287C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720616 | |||||||
chr2:163720791 | C | T | 1 | a0001c0001t0007g0182 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25+14112G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720791 | |||||||
chr2:163720963 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25+13940T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720963 | |||||||
chr2:163720971 | A | AAAAT | 3 | a0001c0001t0003g0106 a0001c0001t0004g0190 a0001c0002t0004g0185 |
3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+13928_25+13931d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720971 | |||||||
chr2:163720986 | G | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+13917C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163720986 | |||||||
chr2:163721002 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
112 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.25+13901C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721002 | |||||||
chr2:163721059 | G | A | 22 | a0001c0001t0001g0137 a0001c0001t0019g0254 a0001c0001t0019g0261 others(19): Show |
22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+13844C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721059 | |||||||
chr2:163721129 | A | G | 5 | a0001c0001t0003g0193 a0001c0001t0004g0192 a0001c0001t0015g0123 others(2): Show |
5 | HG02809.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+13774T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721129 | |||||||
chr2:163721139 | A | G | 1 | a0001c0001t0006g0006 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.25+13764T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721139 | |||||||
chr2:163721191 | A | G | 87 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.25+13712T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721191 | |||||||
chr2:163721198 | T | C | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+13705A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721198 | |||||||
chr2:163721223 | C | T | 9 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+13680G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721223 | |||||||
chr2:163721820 | T | C | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.25+13083A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163721820 | |||||||
chr2:163722213 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(247): Show |
251 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.25+12690T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722213 | |||||||
chr2:163722244 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0006g0076 a0002c0005t0054g0017 |
3 | HG00639.hp2 HG01071.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.25+12659G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722244 | |||||||
chr2:163722325 | A | G | 17 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0102 others(14): Show |
17 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.25+12578T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722325 | |||||||
chr2:163722415 | C | T | 22 | a0001c0001t0001g0137 a0001c0001t0019g0254 a0001c0001t0019g0261 others(19): Show |
22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+12488G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722415 | |||||||
chr2:163722478 | G | GA | 3 | a0001c0001t0005g0174 a0001c0004t0033g0138 a0001c0004t0033g0175 |
3 | HG01070.hp1 HG01071.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.25+12424dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722478 | |||||||
chr2:163722655 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.25+12248A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722655 | |||||||
chr2:163722742 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.25+12161T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722742 | |||||||
chr2:163722754 | G | A | 1 | a0001c0001t0012g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.25+12149C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722754 | |||||||
chr2:163722844 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.25+12059A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722844 | |||||||
chr2:163722879 | A | T | 22 | a0001c0001t0001g0137 a0001c0001t0019g0254 a0001c0001t0019g0261 others(19): Show |
22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+12024T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722879 | |||||||
chr2:163722887 | A | T | 1 | a0001c0001t0007g0182 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25+12016T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722887 | |||||||
chr2:163722925 | G | A | 1 | a0001c0001t0029g0215 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.25+11978C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722925 | |||||||
chr2:163722948 | A | T | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+11955T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722948 | |||||||
chr2:163722993 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+11910G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163722993 | |||||||
chr2:163723013 | T | C | 118 | a0001c0001t0001g0098 a0001c0001t0001g0119 a0001c0001t0001g0139 others(115): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.25+11890A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723013 | |||||||
chr2:163723140 | G | C | 1 | a0001c0001t0004g0226 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.25+11763C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723140 | |||||||
chr2:163723187 | T | A | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+11716A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723187 | |||||||
chr2:163723193 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+11710T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723193 | |||||||
chr2:163723204 | A | ATAC | 6 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0001t0021g0243 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+11698_25+11699i others(5): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723204 | |||||||
chr2:163723213 | TAATAA | T | 1 | a0001c0001t0024g0001 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.25+11685_25+11689d others(7): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723213 | |||||||
chr2:163723241 | G | C | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+11662C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723241 | |||||||
chr2:163723297 | A | T | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+11606T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723297 | |||||||
chr2:163723423 | G | A | 43 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0200 others(40): Show |
43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+11480C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723423 | |||||||
chr2:163723426 | G | A | 2 | a0001c0001t0003g0116 a0001c0001t0005g0117 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.25+11477C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723426 | |||||||
chr2:163723489 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0115 others(7): Show |
10 | HG00735.hp2 HG01175.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+11414G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723489 | |||||||
chr2:163723636 | C | A | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+11267G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723636 | |||||||
chr2:163723827 | T | A | 1 | a0001c0001t0017g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.25+11076A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723827 | |||||||
chr2:163723875 | ATCATCTC others(2): Show |
A | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+11019_25+11027d others(11): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723875 | |||||||
chr2:163723916 | T | G | 1 | a0001c0001t0017g0151 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.25+10987A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163723916 | |||||||
chr2:163724138 | C | T | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+10765G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724138 | |||||||
chr2:163724510 | A | ATTAT | 118 | a0001c0001t0001g0098 a0001c0001t0001g0119 a0001c0001t0001g0139 others(115): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.25+10389_25+10392d others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724510 | |||||||
chr2:163724583 | T | C | 1 | a0001c0001t0022g0083 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.25+10320A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724583 | |||||||
chr2:163724731 | T | G | 118 | a0001c0001t0001g0098 a0001c0001t0001g0119 a0001c0001t0001g0139 others(115): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.25+10172A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724731 | |||||||
chr2:163724811 | A | T | 43 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0200 others(40): Show |
43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+10092T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724811 | |||||||
chr2:163724843 | G | C | 35 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+10060C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724843 | |||||||
chr2:163724851 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.25+10052T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163724851 | |||||||
chr2:163725070 | T | C | 2 | a0001c0001t0003g0105 a0001c0002t0007g0104 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+9833A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725070 | |||||||
chr2:163725071 | T | G | 2 | a0001c0001t0003g0105 a0001c0002t0007g0104 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+9832A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725071 | |||||||
chr2:163725087 | T | G | 15 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0158 others(12): Show |
15 | HG00558.hp2 HG02056.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.25+9816A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725087 | |||||||
chr2:163725250 | A | C | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+9653T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725250 | |||||||
chr2:163725254 | T | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+9649A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725254 | |||||||
chr2:163725280 | A | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+9623T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725280 | |||||||
chr2:163725300 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | NA18943.hp2 NA18959.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.25+9603G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725300 | |||||||
chr2:163725302 | G | A | 16 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0102 others(13): Show |
16 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.25+9601C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725302 | |||||||
chr2:163725481 | A | G | 87 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.25+9422T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725481 | |||||||
chr2:163725556 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+9347G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725556 | |||||||
chr2:163725725 | A | T | 2 | a0001c0001t0003g0105 a0001c0002t0007g0104 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+9178T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725725 | |||||||
chr2:163725764 | C | T | 5 | a0001c0001t0001g0119 a0001c0001t0016g0130 a0001c0001t0024g0001 others(2): Show |
6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+9139G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725764 | |||||||
chr2:163725954 | T | C | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25+8949A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163725954 | |||||||
chr2:163726086 | T | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8817A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726086 | |||||||
chr2:163726467 | A | G | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+8436T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726467 | |||||||
chr2:163726475 | A | G | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+8428T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726475 | |||||||
chr2:163726617 | A | G | 2 | a0001c0001t0034g0250 a0001c0001t0080g0264 |
2 | NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.25+8286T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726617 | |||||||
chr2:163726618 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0077 |
2 | HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.25+8285G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726618 | |||||||
chr2:163726623 | A | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+8280T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726623 | |||||||
chr2:163726850 | T | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8053A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726850 | |||||||
chr2:163726852 | C | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8051G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726852 | |||||||
chr2:163726854 | T | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8049A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726854 | |||||||
chr2:163726859 | T | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8044A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726859 | |||||||
chr2:163726860 | G | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8043C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726860 | |||||||
chr2:163726862 | A | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8041T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726862 | |||||||
chr2:163726865 | G | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8038C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726865 | |||||||
chr2:163726868 | C | T | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25+8035G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726868 | |||||||
chr2:163726870 | A | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8033T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726870 | |||||||
chr2:163726871 | A | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8032T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726871 | |||||||
chr2:163726884 | AAAG | A | 3 | a0001c0001t0001g0115 a0001c0001t0011g0114 a0001c0001t0011g0189 |
3 | HG00735.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.25+8016_25+8018del others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726884 | |||||||
chr2:163726886 | A | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8017T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726886 | |||||||
chr2:163726888 | A | C | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8015T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726888 | |||||||
chr2:163726890 | T | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8013A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726890 | |||||||
chr2:163726891 | A | T | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+8012T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726891 | |||||||
chr2:163726899 | T | G | 1 | a0001c0002t0016g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.25+8004A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726899 | |||||||
chr2:163726906 | T | C | 9 | a0001c0001t0001g0176 a0001c0001t0003g0183 a0001c0001t0005g0174 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+7997A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726906 | |||||||
chr2:163726907 | T | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7996A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726907 | |||||||
chr2:163726910 | T | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7993A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726910 | |||||||
chr2:163726915 | T | A | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7988A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726915 | |||||||
chr2:163726916 | T | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7987A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726916 | |||||||
chr2:163726927 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+7976C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726927 | |||||||
chr2:163726934 | G | T | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7969C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726934 | |||||||
chr2:163726936 | G | T | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7967C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726936 | |||||||
chr2:163726944 | T | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7959A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726944 | |||||||
chr2:163726945 | G | T | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+7958C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726945 | |||||||
chr2:163726955 | T | G | 1 | a0001c0001t0062g0227 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.25+7948A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163726955 | |||||||
chr2:163727143 | T | C | 3 | a0001c0001t0002g0233 a0001c0001t0064g0238 a0001c0001t0076g0068 |
3 | HG02015.hp1 HG02129.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.25+7760A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727143 | |||||||
chr2:163727175 | C | G | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+7728G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727175 | |||||||
chr2:163727300 | A | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(256): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.25+7603T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727300 | |||||||
chr2:163727383 | TA | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
112 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.25+7519delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727383 | |||||||
chr2:163727397 | AT | A | 7 | a0001c0001t0004g0133 a0001c0001t0012g0145 a0001c0001t0031g0131 others(4): Show |
7 | HG02280.hp2 HG02735.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7505delA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727397 | |||||||
chr2:163727404 | T | C | 21 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0102 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+7499A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727404 | |||||||
chr2:163727552 | T | C | 1 | a0001c0001t0012g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25+7351A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727552 | |||||||
chr2:163727632 | C | CCCCACTT others(13): Show |
1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+7251_25+7270dup others(20): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727632 | |||||||
chr2:163727640 | T | G | 2 | a0001c0001t0021g0184 a0001c0002t0013g0191 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.25+7263A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727640 | |||||||
chr2:163727646 | C | G | 35 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.25+7257G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727646 | |||||||
chr2:163727854 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0016g0130 a0001c0001t0024g0001 others(2): Show |
6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+7049C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163727854 | |||||||
chr2:163728116 | T | C | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6787A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728116 | |||||||
chr2:163728175 | C | G | 3 | a0001c0001t0002g0198 a0001c0001t0009g0197 a0001c0001t0043g0210 |
3 | NA18941.hp1 NA18944.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.25+6728G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728175 | |||||||
chr2:163728244 | G | T | 1 | a0001c0001t0050g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.25+6659C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728244 | |||||||
chr2:163728254 | T | TA | 136 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0137 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.25+6648dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728254 | |||||||
chr2:163728397 | A | AAC | 4 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0003g0183 others(1): Show |
4 | HG02698.hp2 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+6504_25+6505dup others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | |||||||
chr2:163728397 | A | AACAC | 13 | a0001c0001t0004g0133 a0001c0001t0011g0173 a0001c0001t0019g0261 others(10): Show |
13 | HG01361.hp2 HG01433.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.25+6502_25+6505dup others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | |||||||
chr2:163728397 | AAC | A | 18 | a0001c0001t0001g0079 a0001c0001t0001g0200 a0001c0001t0002g0005 others(15): Show |
18 | HG01261.hp2 HG01496.hp2 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+6504_25+6505del others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | |||||||
chr2:163728397 | AACAC | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(174): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.25+6502_25+6505del others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | |||||||
chr2:163728397 | AACACAC | A | 6 | a0001c0001t0003g0116 a0001c0001t0005g0117 a0001c0001t0007g0020 others(3): Show |
6 | HG00609.hp1 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+6500_25+6505del others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | |||||||
chr2:163728397 | AACACACA others(1): Show |
A | 18 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0102 others(15): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.25+6498_25+6505del others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728397 | |||||||
chr2:163728483 | A | G | 43 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0200 others(40): Show |
43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.25+6420T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728483 | |||||||
chr2:163728491 | T | C | 6 | a0001c0001t0001g0139 a0001c0001t0003g0162 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+6412A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728491 | |||||||
chr2:163728494 | G | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(159): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.25+6409C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728494 | |||||||
chr2:163728520 | G | A | 3 | a0001c0001t0003g0106 a0001c0001t0004g0190 a0001c0002t0004g0185 |
3 | HG03130.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+6383C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728520 | |||||||
chr2:163728561 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.25+6342T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728561 | |||||||
chr2:163728636 | G | A | 2 | a0001c0001t0003g0105 a0001c0002t0007g0104 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+6267C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728636 | |||||||
chr2:163728774 | C | T | 1 | a0001c0002t0016g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25+6129G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728774 | |||||||
chr2:163728796 | T | C | 1 | a0001c0001t0030g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+6107A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728796 | |||||||
chr2:163728882 | G | A | 1 | a0001c0001t0008g0069 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.25+6021C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728882 | |||||||
chr2:163728986 | C | T | 2 | a0001c0001t0003g0105 a0001c0002t0007g0104 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.25+5917G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163728986 | |||||||
chr2:163729086 | A | C | 22 | a0001c0001t0001g0137 a0001c0001t0019g0254 a0001c0001t0019g0261 others(19): Show |
22 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+5817T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729086 | |||||||
chr2:163729109 | T | C | 1 | a0001c0002t0007g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.25+5794A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729109 | |||||||
chr2:163729122 | T | C | 6 | a0001c0001t0001g0152 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
6 | HG00140.hp1 HG01358.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+5781A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729122 | |||||||
chr2:163729146 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.25+5757G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729146 | |||||||
chr2:163729193 | G | T | 24 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0102 others(21): Show |
24 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+5710C>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729193 | |||||||
chr2:163729324 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+5579T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729324 | |||||||
chr2:163729586 | A | T | 2 | a0001c0001t0009g0128 a0001c0002t0011g0129 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+5317T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729586 | |||||||
chr2:163729722 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.25+5181A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729722 | |||||||
chr2:163729801 | A | G | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+5102T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729801 | |||||||
chr2:163729964 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.25+4939A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163729964 | |||||||
chr2:163730155 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(213): Show |
217 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.25+4748A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730155 | |||||||
chr2:163730172 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0016g0130 a0001c0001t0024g0001 others(2): Show |
6 | HG01261.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+4731C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730172 | |||||||
chr2:163730376 | A | G | 1 | a0001c0002t0011g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.25+4527T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730376 | |||||||
chr2:163730485 | T | C | 1 | a0001c0001t0073g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.25+4418A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730485 | |||||||
chr2:163730500 | G | A | 20 | a0001c0001t0019g0254 a0001c0001t0019g0261 a0001c0001t0019g0262 others(17): Show |
20 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.25+4403C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730500 | |||||||
chr2:163730504 | T | G | 1 | a0001c0001t0020g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.25+4399A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730504 | T | TTG | 47 | a0001c0001t0001g0118 a0001c0001t0001g0140 a0001c0001t0001g0141 others(44): Show |
47 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.25+4397_25+4398dup others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730504 | T | TTGTG | 54 | a0001c0001t0001g0111 a0001c0001t0001g0139 a0001c0001t0001g0196 others(51): Show |
54 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.25+4395_25+4398dup others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730504 | T | TTGTGTG | 17 | a0001c0001t0001g0236 a0001c0001t0002g0223 a0001c0001t0004g0225 others(14): Show |
17 | HG00558.hp1 HG00609.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.25+4393_25+4398dup others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730504 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0176 a0001c0001t0001g0228 a0001c0001t0003g0183 others(6): Show |
9 | HG01106.hp1 HG02056.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+4391_25+4398dup others(8): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730504 | TTG | T | 8 | a0001c0001t0001g0137 a0001c0001t0004g0190 a0001c0001t0012g0122 others(5): Show |
8 | HG01255.hp1 HG01261.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+4397_25+4398del others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730504 | TTGTG | T | 6 | a0001c0001t0004g0133 a0001c0001t0031g0131 a0001c0002t0007g0135 others(3): Show |
6 | HG02280.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+4395_25+4398del others(4): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730504 | TTGTGTG | T | 8 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(5): Show |
8 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+4393_25+4398del others(6): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730504 | |||||||
chr2:163730524 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.25+4379C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730524 | |||||||
chr2:163730662 | T | G | 1 | a0001c0001t0012g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.25+4241A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730662 | |||||||
chr2:163730687 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.25+4216T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730687 | |||||||
chr2:163730762 | A | G | 135 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0139 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.25+4141T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730762 | |||||||
chr2:163730769 | A | G | 2 | a0001c0001t0035g0246 a0001c0008t0035g0248 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.25+4134T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730769 | |||||||
chr2:163730826 | A | G | 2 | a0001c0001t0002g0005 a0001c0001t0032g0014 |
2 | NA18969.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.25+4077T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730826 | |||||||
chr2:163730884 | C | T | 3 | a0001c0001t0003g0183 a0001c0001t0007g0182 a0001c0001t0011g0173 |
3 | HG02258.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.25+4019G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730884 | |||||||
chr2:163730937 | A | G | 21 | a0001c0001t0019g0254 a0001c0001t0019g0261 a0001c0001t0019g0262 others(18): Show |
21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+3966T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730937 | |||||||
chr2:163730985 | G | A | 3 | a0001c0001t0003g0105 a0001c0001t0003g0106 a0001c0002t0007g0104 |
3 | HG02818.hp1 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+3918C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730985 | |||||||
chr2:163730991 | A | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0077 |
2 | HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.25+3912T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163730991 | |||||||
chr2:163731031 | C | CA | 6 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0001t0021g0243 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+3871dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731031 | |||||||
chr2:163731035 | T | C | 1 | a0001c0001t0008g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.25+3868A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731035 | |||||||
chr2:163731450 | T | C | 135 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0139 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.25+3453A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731450 | |||||||
chr2:163731455 | C | T | 1 | a0001c0001t0031g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.25+3448G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731455 | |||||||
chr2:163731594 | G | A | 6 | a0001c0001t0001g0115 a0001c0001t0003g0187 a0001c0001t0011g0114 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+3309C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731594 | |||||||
chr2:163731612 | A | G | 2 | a0001c0001t0026g0094 a0001c0001t0026g0095 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.25+3291T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731612 | |||||||
chr2:163731714 | GA | G | 37 | a0001c0001t0001g0012 a0001c0001t0001g0115 a0001c0001t0001g0139 others(34): Show |
37 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.25+3188delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731714 | |||||||
chr2:163731791 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25+3112T>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731791 | |||||||
chr2:163731999 | CA | C | 21 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0102 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+2903delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163731999 | |||||||
chr2:163732179 | C | T | 2 | a0001c0001t0035g0246 a0001c0008t0035g0248 |
2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.25+2724G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732179 | |||||||
chr2:163732401 | TA | T | 21 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0102 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+2501delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732401 | |||||||
chr2:163732457 | T | C | 87 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.25+2446A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732457 | |||||||
chr2:163732699 | C | A | 1 | a0001c0001t0004g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.25+2204G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732699 | |||||||
chr2:163732705 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.25+2198A>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163732705 | |||||||
chr2:163733098 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(125): Show |
128 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.25+1805A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733098 | |||||||
chr2:163733109 | AC | A | 4 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0089 others(1): Show |
4 | HG02074.hp2 NA18946.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1793delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733109 | |||||||
chr2:163733202 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.25+1701C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733202 | |||||||
chr2:163733256 | C | T | 1 | a0001c0001t0046g0013 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.25+1647G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733256 | |||||||
chr2:163733378 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+1525G>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733378 | |||||||
chr2:163733613 | G | A | 3 | a0001c0001t0003g0183 a0001c0001t0007g0182 a0001c0001t0011g0173 |
3 | HG02258.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.25+1290C>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733613 | |||||||
chr2:163733746 | C | T | 3 | a0001c0001t0003g0183 a0001c0001t0007g0182 a0001c0001t0011g0173 |
3 | HG02258.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.25+1157G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733746 | |||||||
chr2:163733804 | G | C | 1 | a0001c0001t0006g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.25+1099C>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733804 | |||||||
chr2:163733942 | C | CA | 21 | a0001c0001t0001g0118 a0001c0001t0019g0254 a0001c0001t0019g0261 others(18): Show |
21 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.25+960dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733942 | |||||||
chr2:163733942 | CA | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(162): Show |
165 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.25+960delT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733942 | |||||||
chr2:163733942 | CAA | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0110 a0001c0001t0001g0119 others(22): Show |
26 | HG01167.hp1 HG01261.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.25+959_25+960delTT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163733942 | |||||||
chr2:163734115 | C | CT | 35 | a0001c0001t0001g0098 a0001c0001t0001g0196 a0001c0001t0001g0199 others(32): Show |
35 | HG00423.hp1 HG02055.hp2 HG02258.hp2 others(32): Show |
intron_variant | MODIFIER | c.25+787dupA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734115 | |||||||
chr2:163734115 | C | CTT | 9 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0001t0021g0243 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+786_25+787dupAA | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734115 | |||||||
chr2:163734341 | GC | G | 44 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.25+561delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734341 | |||||||
chr2:163734350 | A | C | 25 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0003g0097 others(22): Show |
25 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.25+553T>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734350 | |||||||
chr2:163734541 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+362G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734541 | |||||||
chr2:163734557 | C | CA | 14 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0003g0116 others(11): Show |
15 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+345dupT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | |||||||
chr2:163734557 | C | CAA | 40 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(37): Show |
40 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.25+344_25+345dupTT | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | |||||||
chr2:163734557 | C | CAAA | 150 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(147): Show |
150 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.25+343_25+345dupTT others(1): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | |||||||
chr2:163734557 | C | CAAAA | 22 | a0001c0001t0001g0236 a0001c0001t0002g0088 a0001c0001t0002g0089 others(19): Show |
22 | HG02015.hp1 HG02040.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+342_25+345dupTT others(2): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | |||||||
chr2:163734557 | C | CAAAAA | 7 | a0001c0001t0003g0187 a0001c0001t0004g0190 a0001c0001t0011g0189 others(4): Show |
7 | HG01175.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+341_25+345dupTT others(3): Show |
FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734557 | |||||||
chr2:163734628 | T | C | 2 | a0001c0001t0003g0193 a0001c0001t0004g0192 |
2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+275A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734628 | |||||||
chr2:163734771 | T | C | 1 | a0001c0001t0013g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+132A>G | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734771 | |||||||
chr2:163734781 | A | T | 1 | a0001c0001t0001g0002 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+122T>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 2/2 | chr2 | 163734781 | |||||||
chr2:163735277 | C | A | 1 | a0001c0001t0067g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-145-205G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735277 | |||||||
chr2:163735316 | AC | A | 43 | a0001c0001t0001g0196 a0001c0001t0001g0199 a0001c0001t0001g0200 others(40): Show |
43 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-145-245delG | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735316 | |||||||
chr2:163735317 | C | A | 1 | a0001c0001t0065g0156 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-145-245G>T | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735317 | |||||||
chr2:163735377 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-145-305G>A | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735377 | |||||||
chr2:163735774 | T | G | 6 | a0001c0001t0003g0240 a0001c0001t0006g0239 a0001c0001t0021g0243 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146+64A>C | FIGN | ENSG00000182263.14 | transcript | ENST00000333129.4 | protein_coding | 1/2 | chr2 | 163735774 |