Item | Value |
---|---|
geneid | 6619 |
ensemblid | ENSG00000164975.16 |
hgncid | 11136 |
symbol | SNAPC3 |
name | small nuclear RNA activating complex polypeptide 3 |
refseq_nuc | NM_001039697.2 |
refseq_prot | NP_001034786.1 |
ensembl_nuc | ENST00000380821.8 |
ensembl_prot | ENSP00000370200.3 |
mane_status | MANE Select |
chr | chr9 |
start | 15422876 |
end | 15461626 |
strand | + |
ver | v1.2 |
region | chr9:15422876-15461626 |
region5000 | chr9:15417876-15466626 |
regionname0 | SNAPC3_chr9_15422876_15461626 |
regionname5000 | SNAPC3_chr9_15417876_15466626 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 411 | 291 | 71 | 47 | 131 | 4 | 36 | 98 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | MAEGS others(406): Show |
chr9 | 15417876 | 15466626 |
a0002 | 0/0 | 411 | 8 | 4 | 3 | 0 | 0 | 1 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | MAEGS others(406): Show |
chr9 | 15417876 | 15466626 |
a0003 | 0/0 | 411 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | MAEGS others(406): Show |
chr9 | 15417876 | 15466626 |
a0004 | 0/0 | 411 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | MAEGS others(406): Show |
chr9 | 15417876 | 15466626 |
a0005 | 0/0 | 411 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | MAEGS others(406): Show |
chr9 | 15417876 | 15466626 |
a0006 | 0/0 | 411 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | MAEGS others(406): Show |
chr9 | 15417876 | 15466626 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1233 | 277 | 58 | 46 | 131 | 4 | 36 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 | ||
a0001c0002 | 0/0 | 1233 | 13 | 12 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 | ||
a0001c0006 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 | ||
a0002c0003 | 0/0 | 1233 | 8 | 4 | 3 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 | ||
a0003c0004 | 0/0 | 1233 | 6 | 6 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 | ||
a0004c0005 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 | ||
a0005c0007 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 | ||
a0006c0008 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | ATGGC others(1228): Show |
chr9 | 15417876 | 15466626 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3000 | 151 | 19 | 35 | 74 | 3 | 19 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0002 | 1/0 | 3000 | 38 | 0 | 1 | 25 | 1 | 10 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0003 | 0/0 | 3000 | 29 | 2 | 1 | 23 | 0 | 3 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0004 | 0/0 | 3000 | 15 | 10 | 3 | 1 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0005 | 0/0 | 3000 | 13 | 12 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0006 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0007 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0008 | 0/0 | 3000 | 6 | 5 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0009 | 0/0 | 3000 | 4 | 4 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0010 | 0/0 | 3000 | 2 | 2 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0011 | 0/0 | 3000 | 2 | 0 | 2 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0012 | 0/0 | 3000 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0013 | 0/0 | 3000 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0014 | 0/0 | 3000 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0015 | 0/0 | 3000 | 2 | 0 | 0 | 0 | 0 | 2 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0017 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0018 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0019 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0020 | 0/0 | 3000 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0021 | 0/0 | 3000 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0022 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0001t0023 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2974): Show |
chr9 | 15417876 | 15466626 |
a0001c0002t0006 | 0/0 | 3000 | 12 | 12 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0002t0016 | 0/0 | 3000 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0001c0006t0005 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0002c0003t0007 | 0/0 | 3000 | 8 | 4 | 3 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0003c0004t0001 | 0/0 | 3000 | 6 | 6 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0004c0005t0001 | 0/0 | 3000 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0005c0007t0001 | 0/0 | 3000 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
a0006c0008t0001 | 0/0 | 3000 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | GAACA others(2995): Show |
chr9 | 15417876 | 15466626 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0001 | 0/0 | 8 | 0 | 0 | 4 | 0 | 4 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0023 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0008g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0008g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0009g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0011g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0011g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0013g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0013g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0014g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0014g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0015g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0015g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0017g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0018g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0019g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0021g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0022g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0001t0023g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0002t0016g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0001c0006t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0002c0003t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0002c0003t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0002c0003t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0002c0003t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0002c0003t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0002c0003t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0003c0004t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0003c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0003c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0003c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0004c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0005c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
a0006c0008t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0233 | EUR | FIN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01069 | hp2 | a0002 | c0003 | t0007 | g0167 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01071 | hp2 | a0002 | c0003 | t0007 | g0168 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01167 | hp1 | a0001 | c0001 | t0011 | g0069 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01192 | hp1 | a0001 | c0001 | t0011 | g0070 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01243 | hp2 | a0001 | c0002 | t0016 | g0249 | AMR | PUR | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01361 | hp2 | a0002 | c0003 | t0007 | g0170 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0016 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01884 | hp1 | a0001 | c0002 | t0006 | g0251 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0220 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01891 | hp1 | a0002 | c0003 | t0007 | g0008 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG01993 | hp2 | a0001 | c0001 | t0021 | g0213 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02055 | hp1 | a0001 | c0001 | t0019 | g0137 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02080 | hp2 | a0004 | c0005 | t0001 | g0132 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02135 | hp2 | a0001 | c0001 | t0013 | g0235 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CDX | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02258 | hp2 | a0001 | c0002 | t0006 | g0028 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02273 | hp2 | a0001 | c0001 | t0020 | g0057 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02280 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02523 | hp1 | a0001 | c0001 | t0014 | g0202 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02647 | hp1 | a0001 | c0002 | t0006 | g0252 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02683 | hp1 | a0005 | c0007 | t0001 | g0112 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02698 | hp1 | a0001 | c0001 | t0018 | g0160 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0166 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0136 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02818 | hp1 | a0001 | c0002 | t0006 | g0253 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0030 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02886 | hp2 | a0002 | c0003 | t0007 | g0171 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02895 | hp1 | a0001 | c0002 | t0006 | g0029 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02896 | hp2 | a0001 | c0002 | t0006 | g0029 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02897 | hp2 | a0001 | c0002 | t0006 | g0247 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02965 | hp2 | a0002 | c0003 | t0007 | g0008 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0157 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0172 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03041 | hp1 | a0001 | c0002 | t0006 | g0028 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03041 | hp2 | a0001 | c0002 | t0006 | g0031 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0065 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03139 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0159 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03195 | hp2 | a0003 | c0004 | t0001 | g0243 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | MSL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | MSL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03486 | hp2 | a0001 | c0001 | t0023 | g0218 | AFR | MSL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | ESN | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03669 | hp2 | a0001 | c0001 | t0015 | g0206 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03688 | hp1 | a0001 | c0001 | t0015 | g0207 | SAS | STU | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03710 | hp1 | a0002 | c0003 | t0007 | g0169 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | STU | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | STU | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18522 | hp1 | a0002 | c0003 | t0007 | g0008 | AFR | YRI | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18522 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | YRI | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CHB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18906 | hp1 | a0001 | c0002 | t0006 | g0250 | AFR | YRI | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18906 | hp2 | a0001 | c0002 | t0006 | g0032 | AFR | YRI | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18972 | hp2 | a0001 | c0001 | t0022 | g0216 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18983 | hp1 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18986 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18989 | hp1 | a0001 | c0001 | t0014 | g0215 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18992 | hp1 | a0001 | c0001 | t0017 | g0146 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | LWK | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19030 | hp2 | a0006 | c0008 | t0001 | g0088 | AFR | LWK | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19087 | hp1 | a0001 | c0001 | t0013 | g0234 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | YRI | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | YRI | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0181 | AFR | ASW | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02109 | hp1 | a0003 | c0004 | t0001 | g0242 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02486 | hp2 | a0003 | c0004 | t0001 | g0244 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG02559 | hp2 | a0001 | c0006 | t0005 | g0184 | AFR | ACB | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | MSL | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | USA | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0067 | REF | REF | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0023 | REF | REF | SNAPC3_chr9_15417876_15466626 | SNAPC3 | chr9 | 15417876 | 15466626 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:15422959 | G | A | 1 | a0003 | 6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
missense_variant | MODERATE | c.80G>A | p.Cys27Tyr | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/9 | 84/3000 | 80/1236 | 27/411 | chr9 | 15422959 | |||
chr9:15423048 | G | C | 1 | a0004 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.169G>C | p.Gly57Arg | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/9 | 173/3000 | 169/1236 | 57/411 | chr9 | 15423048 | |||
chr9:15459732 | A | C | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1102A>C | p.Asn368His | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1106/3000 | 1102/1236 | 368/411 | chr9 | 15459732 | |||
chr9:15459784 | G | A | 1 | a0005 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1154G>A | p.Arg385Gln | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1158/3000 | 1154/1236 | 385/411 | chr9 | 15459784 | |||
chr9:15459823 | A | C | 1 | a0002 | 8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
missense_variant | MODERATE | c.1193A>C | p.Glu398Ala | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1197/3000 | 1193/1236 | 398/411 | chr9 | 15459823 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:15453140 | G | A | 1 | a0001c0002 | 13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
synonymous_variant | LOW | c.915G>A | p.Leu305Leu | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/9 | 919/3000 | 915/1236 | 305/411 | chr9 | 15453140 | |||
chr9:15459728 | G | C | 1 | a0001c0006 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1098G>C | p.Thr366Thr | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1102/3000 | 1098/1236 | 366/411 | chr9 | 15459728 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:15459864 | TAAGAATA others(14): Show |
T | 1 | a0001c0001t0023 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1_*21delGAATAGCTA others(12): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1 | INFO_REALIGN_3_PRIME | chr9 | 15459864 | |||||
chr9:15460004 | G | C | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(20): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*138G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 138 | chr9 | 15460004 | ||||||
chr9:15460076 | A | G | 1 | a0001c0001t0020 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 210 | chr9 | 15460076 | ||||||
chr9:15460447 | G | A | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(25): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*581G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 581 | chr9 | 15460447 | ||||||
chr9:15460476 | C | T | 2 | a0001c0001t0005 a0001c0006t0005 |
14 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*610C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 610 | chr9 | 15460476 | ||||||
chr9:15460477 | G | A | 1 | a0001c0001t0010 | 2 | HG02970.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*611G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 611 | chr9 | 15460477 | ||||||
chr9:15460680 | C | T | 1 | a0001c0001t0012 | 2 | NA18983.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*814C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 814 | chr9 | 15460680 | ||||||
chr9:15460686 | C | T | 1 | a0001c0001t0008 | 6 | HG01433.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*820C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 820 | chr9 | 15460686 | ||||||
chr9:15460912 | A | G | 1 | a0001c0001t0019 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1046A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1046 | chr9 | 15460912 | ||||||
chr9:15461140 | A | G | 3 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0022 |
4 | HG01167.hp1 HG01192.hp1 HG01993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1274A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1274 | chr9 | 15461140 | ||||||
chr9:15461223 | G | C | 1 | a0001c0001t0009 | 4 | HG02922.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1357G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1357 | chr9 | 15461223 | ||||||
chr9:15461227 | T | G | 1 | a0001c0002t0016 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1361 | chr9 | 15461227 | ||||||
chr9:15461431 | C | G | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0016 |
14 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1565C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1565 | chr9 | 15461431 | ||||||
chr9:15461441 | C | T | 1 | a0001c0001t0018 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1575C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1575 | chr9 | 15461441 | ||||||
chr9:15461453 | C | T | 1 | a0001c0001t0015 | 2 | HG03669.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1587C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1587 | chr9 | 15461453 | ||||||
chr9:15461473 | C | A | 3 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0018 |
18 | HG00544.hp1 HG00735.hp2 HG00741.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1607C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1607 | chr9 | 15461473 | ||||||
chr9:15461508 | T | C | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(14): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1642T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1642 | chr9 | 15461508 | ||||||
chr9:15461567 | T | C | 1 | a0001c0001t0017 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1701T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1701 | chr9 | 15461567 | ||||||
chr9:15461620 | C | G | 1 | a0001c0001t0023 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1754C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 9/9 | 1754 | chr9 | 15461620 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:15423260 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.314+67C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423260 | |||||||
chr9:15423314 | T | C | 3 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.314+121T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423314 | |||||||
chr9:15423359 | A | G | 12 | a0001c0001t0001g0248 a0001c0002t0006g0028 a0001c0002t0006g0029 others(9): Show |
14 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.314+166A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423359 | |||||||
chr9:15423397 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.314+204G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423397 | |||||||
chr9:15423479 | A | G | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+286A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423479 | |||||||
chr9:15423550 | G | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.314+357G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423550 | |||||||
chr9:15423684 | A | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
10 | HG00642.hp1 HG01081.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-225A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423684 | |||||||
chr9:15423878 | C | G | 1 | a0001c0001t0002g0027 | 2 | HG02015.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.315-31C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 1/8 | chr9 | 15423878 | |||||||
chr9:15424118 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
6 | HG02083.hp2 HG02155.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+132G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424118 | |||||||
chr9:15424293 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.392+307G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424293 | |||||||
chr9:15424373 | G | C | 1 | a0001c0001t0003g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.392+387G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424373 | |||||||
chr9:15424399 | A | G | 2 | a0001c0001t0005g0240 a0001c0001t0005g0241 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.392+413A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424399 | |||||||
chr9:15424452 | T | C | 3 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0247 |
5 | HG02258.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.392+466T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424452 | |||||||
chr9:15424542 | AAC | A | 15 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.392+560_392+561del others(2): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15424542 | ||||||
chr9:15424623 | G | C | 12 | a0001c0001t0001g0248 a0001c0002t0006g0028 a0001c0002t0006g0029 others(9): Show |
14 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.392+637G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424623 | |||||||
chr9:15424713 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.392+727A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424713 | |||||||
chr9:15424758 | T | G | 2 | a0001c0001t0005g0240 a0001c0001t0005g0241 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.392+772T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424758 | |||||||
chr9:15424781 | C | T | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | NA18982.hp1 NA18987.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.392+795C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424781 | |||||||
chr9:15424890 | T | C | 32 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0039 others(29): Show |
33 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.392+904T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424890 | |||||||
chr9:15424894 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.392+908C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424894 | |||||||
chr9:15424940 | G | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(227): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.392+954G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424940 | |||||||
chr9:15424982 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.392+996C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15424982 | |||||||
chr9:15425017 | A | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.392+1031A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425017 | |||||||
chr9:15425220 | T | C | 1 | a0001c0001t0008g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.392+1234T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425220 | |||||||
chr9:15425225 | C | T | 11 | a0001c0001t0003g0183 a0001c0001t0005g0185 a0001c0001t0005g0186 others(8): Show |
11 | HG01074.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.392+1239C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425225 | |||||||
chr9:15425702 | A | G | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0004g0004 others(9): Show |
16 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.392+1716A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425702 | |||||||
chr9:15425725 | G | T | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.392+1739G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425725 | |||||||
chr9:15425847 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.392+1861G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425847 | |||||||
chr9:15425893 | C | T | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.392+1907C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425893 | |||||||
chr9:15425936 | A | C | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | NA18942.hp2 NA18960.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.392+1950A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15425936 | |||||||
chr9:15426083 | A | G | 1 | a0001c0001t0023g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.392+2097A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426083 | |||||||
chr9:15426105 | C | T | 1 | a0001c0001t0006g0246 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.392+2119C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426105 | |||||||
chr9:15426143 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.392+2157C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426143 | |||||||
chr9:15426253 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.392+2267G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426253 | |||||||
chr9:15426330 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.392+2344C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426330 | |||||||
chr9:15426477 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.392+2491T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426477 | |||||||
chr9:15426574 | A | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.392+2588A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426574 | |||||||
chr9:15426643 | C | T | 5 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+2657C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426643 | |||||||
chr9:15426671 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.392+2685A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426671 | |||||||
chr9:15426767 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(227): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.392+2781T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426767 | |||||||
chr9:15426770 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.392+2784G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426770 | |||||||
chr9:15426855 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.392+2869G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426855 | |||||||
chr9:15426901 | T | C | 17 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0004g0156 others(14): Show |
18 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.392+2915T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15426901 | |||||||
chr9:15427011 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.392+3025T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427011 | |||||||
chr9:15427016 | TTATTA | T | 4 | a0002c0003t0007g0167 a0002c0003t0007g0168 a0002c0003t0007g0169 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.392+3038_392+3042d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15427016 | ||||||
chr9:15427134 | G | C | 3 | a0001c0001t0001g0071 a0001c0001t0011g0069 a0001c0001t0011g0070 |
3 | HG00642.hp2 HG01167.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.392+3148G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427134 | |||||||
chr9:15427172 | A | C | 1 | a0001c0001t0003g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.392+3186A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427172 | |||||||
chr9:15427190 | C | A | 5 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.392+3204C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427190 | |||||||
chr9:15427279 | T | C | 28 | a0001c0001t0001g0248 a0001c0001t0003g0183 a0001c0001t0004g0022 others(25): Show |
31 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.392+3293T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427279 | |||||||
chr9:15427346 | G | A | 26 | a0001c0001t0002g0205 a0001c0001t0003g0005 a0001c0001t0003g0010 others(23): Show |
31 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.392+3360G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427346 | |||||||
chr9:15427466 | A | C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | NA18942.hp2 NA18960.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.392+3480A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427466 | |||||||
chr9:15427471 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.392+3485C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427471 | |||||||
chr9:15427534 | G | C | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.392+3548G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427534 | |||||||
chr9:15427622 | C | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0238 a0001c0001t0002g0239 |
5 | HG00408.hp1 HG02074.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.392+3636C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427622 | |||||||
chr9:15427655 | A | G | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.392+3669A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427655 | |||||||
chr9:15427792 | A | G | 13 | a0001c0001t0002g0237 a0001c0001t0004g0007 a0001c0001t0004g0156 others(10): Show |
15 | HG00544.hp1 HG00735.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.392+3806A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427792 | |||||||
chr9:15427810 | A | T | 13 | a0001c0001t0002g0237 a0001c0001t0004g0007 a0001c0001t0004g0156 others(10): Show |
15 | HG00544.hp1 HG00735.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.392+3824A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427810 | |||||||
chr9:15427817 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.392+3831T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427817 | |||||||
chr9:15427926 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.392+3940T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427926 | |||||||
chr9:15427944 | C | G | 2 | a0001c0001t0004g0165 a0001c0001t0004g0166 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.392+3958C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15427944 | |||||||
chr9:15428067 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.392+4081C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428067 | |||||||
chr9:15428073 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.392+4087T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428073 | |||||||
chr9:15428111 | C | CA | 17 | a0001c0001t0001g0175 a0001c0001t0002g0221 a0001c0001t0002g0222 others(14): Show |
18 | HG01074.hp1 HG01106.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.392+4147dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15428111 | ||||||
chr9:15428111 | CA | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(168): Show |
203 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.392+4147delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15428111 | ||||||
chr9:15428173 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.392+4187G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428173 | |||||||
chr9:15428279 | G | A | 9 | a0001c0001t0003g0183 a0001c0001t0005g0185 a0001c0001t0005g0186 others(6): Show |
9 | HG01074.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.392+4293G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428279 | |||||||
chr9:15428279 | G | C | 2 | a0001c0001t0005g0191 a0001c0001t0005g0192 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.392+4293G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428279 | |||||||
chr9:15428286 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.392+4300A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428286 | |||||||
chr9:15428365 | C | T | 1 | a0001c0001t0019g0137 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.392+4379C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428365 | |||||||
chr9:15428369 | C | T | 1 | a0001c0001t0008g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.392+4383C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428369 | |||||||
chr9:15428381 | C | T | 4 | a0001c0001t0005g0187 a0001c0001t0005g0188 a0001c0001t0005g0189 others(1): Show |
4 | HG02280.hp2 HG02895.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.392+4395C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428381 | |||||||
chr9:15428492 | C | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.392+4506C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428492 | |||||||
chr9:15428508 | C | CA | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(137): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.392+4537dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15428508 | ||||||
chr9:15428508 | C | CAA | 8 | a0001c0001t0001g0074 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02165.hp2 NA18942.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.392+4536_392+4537d others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15428508 | ||||||
chr9:15428534 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.392+4548A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428534 | |||||||
chr9:15428634 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.392+4648A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15428634 | |||||||
chr9:15428970 | G | GA | 6 | a0001c0001t0001g0043 a0001c0001t0001g0075 a0001c0001t0001g0084 others(3): Show |
6 | HG00741.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.393-4573dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15428970 | ||||||
chr9:15429031 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.393-4521T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429031 | |||||||
chr9:15429194 | G | GT | 13 | a0001c0001t0001g0074 a0001c0001t0001g0248 a0001c0002t0006g0028 others(10): Show |
15 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.393-4349dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15429194 | ||||||
chr9:15429354 | G | C | 1 | a0001c0001t0007g0220 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.393-4198G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429354 | |||||||
chr9:15429400 | T | G | 53 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(50): Show |
59 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.393-4152T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429400 | |||||||
chr9:15429483 | A | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG01981.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.393-4069A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429483 | |||||||
chr9:15429539 | GA | G | 15 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.393-4005delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15429539 | ||||||
chr9:15429541 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(153): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.393-4011A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429541 | |||||||
chr9:15429732 | C | A | 3 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 |
3 | NA18990.hp1 NA19064.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.393-3820C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429732 | |||||||
chr9:15429852 | A | G | 1 | a0001c0001t0013g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.393-3700A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429852 | |||||||
chr9:15429856 | A | G | 7 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0002c0003t0007g0008 others(4): Show |
9 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-3696A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15429856 | |||||||
chr9:15430188 | G | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
268 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.393-3364G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430188 | |||||||
chr9:15430240 | C | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.393-3312C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430240 | |||||||
chr9:15430287 | C | T | 1 | a0001c0001t0023g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.393-3265C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430287 | |||||||
chr9:15430426 | T | A | 1 | a0001c0001t0003g0183 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.393-3126T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430426 | |||||||
chr9:15430515 | A | T | 3 | a0001c0001t0002g0027 a0001c0001t0013g0234 a0001c0001t0013g0235 |
4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.393-3037A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430515 | |||||||
chr9:15430690 | G | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.393-2862G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430690 | |||||||
chr9:15430782 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.393-2770G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430782 | |||||||
chr9:15430808 | A | T | 1 | a0001c0001t0005g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.393-2744A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430808 | |||||||
chr9:15430956 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.393-2596A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15430956 | |||||||
chr9:15431141 | C | G | 1 | a0004c0005t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.393-2411C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431141 | |||||||
chr9:15431156 | C | T | 11 | a0001c0001t0003g0183 a0001c0001t0005g0185 a0001c0001t0005g0186 others(8): Show |
11 | HG01074.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.393-2396C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431156 | |||||||
chr9:15431289 | G | A | 1 | a0001c0001t0005g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393-2263G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431289 | |||||||
chr9:15431328 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.393-2224C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431328 | |||||||
chr9:15431386 | C | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(250): Show |
303 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.393-2166C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431386 | |||||||
chr9:15431591 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.393-1961C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431591 | |||||||
chr9:15431724 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.393-1828C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431724 | |||||||
chr9:15431821 | G | C | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.393-1731G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431821 | |||||||
chr9:15431843 | A | C | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.393-1709A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431843 | |||||||
chr9:15431884 | C | CT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(103): Show |
118 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.393-1645dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15431884 | ||||||
chr9:15431884 | C | CTT | 15 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.393-1646_393-1645d others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15431884 | ||||||
chr9:15431884 | CT | C | 8 | a0001c0001t0001g0143 a0001c0001t0002g0225 a0001c0001t0002g0238 others(5): Show |
10 | HG01433.hp1 HG02809.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.393-1645delT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15431884 | ||||||
chr9:15431925 | G | GCATAT | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.393-1623_393-1619d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15431925 | ||||||
chr9:15431954 | A | C | 1 | a0001c0001t0002g0027 | 2 | HG02015.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.393-1598A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15431954 | |||||||
chr9:15431966 | ATTG | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0039 others(21): Show |
25 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.393-1583_393-1581d others(5): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15431966 | ||||||
chr9:15432072 | G | C | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.393-1480G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432072 | |||||||
chr9:15432096 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG00099.hp1 HG02683.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.393-1456A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432096 | |||||||
chr9:15432227 | C | G | 15 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.393-1325C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432227 | |||||||
chr9:15432246 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(173): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.393-1306T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432246 | |||||||
chr9:15432283 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0059 |
2 | NA18952.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.393-1269A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432283 | |||||||
chr9:15432443 | C | G | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.393-1109C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432443 | |||||||
chr9:15432671 | T | C | 5 | a0001c0001t0003g0010 a0001c0001t0003g0196 a0001c0001t0003g0203 others(2): Show |
7 | NA18964.hp2 NA18972.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.393-881T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432671 | |||||||
chr9:15432764 | A | G | 3 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0247 |
5 | HG02258.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.393-788A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15432764 | |||||||
chr9:15433133 | A | G | 4 | a0001c0001t0005g0181 a0001c0001t0005g0182 a0001c0001t0005g0240 others(1): Show |
4 | HG02109.hp2 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-419A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15433133 | |||||||
chr9:15433232 | A | C | 1 | a0001c0001t0004g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.393-320A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15433232 | |||||||
chr9:15433241 | A | T | 1 | a0001c0001t0002g0223 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.393-311A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15433241 | |||||||
chr9:15433271 | G | GA | 16 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0005g0240 others(13): Show |
18 | HG01175.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.393-268dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15433271 | ||||||
chr9:15433271 | GA | G | 7 | a0001c0001t0005g0193 a0002c0003t0007g0008 a0002c0003t0007g0167 others(4): Show |
9 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.393-268delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15433271 | ||||||
chr9:15433286 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.393-266G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15433286 | |||||||
chr9:15433357 | TG | T | 5 | a0001c0001t0003g0212 a0001c0001t0003g0214 a0001c0001t0014g0202 others(2): Show |
5 | HG01361.hp1 HG01993.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.393-194delG | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15433357 | |||||||
chr9:15433429 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(175): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.393-123T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15433429 | |||||||
chr9:15433500 | G | A | 1 | a0004c0005t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.393-52G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | chr9 | 15433500 | |||||||
chr9:15433522 | A | AT | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.393-19dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 15433522 | ||||||
chr9:15433688 | A | T | 1 | a0001c0001t0003g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.477+52A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15433688 | |||||||
chr9:15433846 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.477+210C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15433846 | |||||||
chr9:15433878 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.477+242G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15433878 | |||||||
chr9:15434066 | AGGCACTG others(4): Show |
A | 11 | a0001c0001t0003g0183 a0001c0001t0005g0185 a0001c0001t0005g0186 others(8): Show |
11 | HG01074.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.477+437_477+447del others(11): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15434066 | ||||||
chr9:15434105 | A | T | 1 | a0001c0001t0008g0016 | 2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.477+469A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434105 | |||||||
chr9:15434114 | C | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(162): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.477+478C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434114 | |||||||
chr9:15434409 | C | CT | 21 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0074 others(18): Show |
24 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.477+789dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15434409 | ||||||
chr9:15434543 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.477+907G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434543 | |||||||
chr9:15434561 | C | G | 2 | a0001c0001t0004g0165 a0001c0001t0004g0166 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.477+925C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434561 | |||||||
chr9:15434563 | A | G | 27 | a0001c0001t0002g0205 a0001c0001t0003g0005 a0001c0001t0003g0010 others(24): Show |
32 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.477+927A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434563 | |||||||
chr9:15434758 | G | A | 15 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.477+1122G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434758 | |||||||
chr9:15434794 | C | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.477+1158C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434794 | |||||||
chr9:15434828 | A | G | 1 | a0001c0001t0023g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.477+1192A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434828 | |||||||
chr9:15434855 | C | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.477+1219C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434855 | |||||||
chr9:15434964 | T | C | 1 | a0001c0001t0007g0220 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.477+1328T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15434964 | |||||||
chr9:15435237 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.477+1601T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435237 | |||||||
chr9:15435278 | A | G | 1 | a0004c0005t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.477+1642A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435278 | |||||||
chr9:15435280 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.477+1644A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435280 | |||||||
chr9:15435398 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.477+1762C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435398 | |||||||
chr9:15435430 | G | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.477+1794G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435430 | |||||||
chr9:15435455 | C | G | 1 | a0001c0001t0005g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.477+1819C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435455 | |||||||
chr9:15435488 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.477+1852G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435488 | |||||||
chr9:15435539 | C | T | 1 | a0001c0001t0004g0022 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.477+1903C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435539 | |||||||
chr9:15435592 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.477+1956G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435592 | |||||||
chr9:15435600 | A | T | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+1964A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435600 | |||||||
chr9:15435643 | C | G | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.477+2007C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435643 | |||||||
chr9:15435660 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.477+2024T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435660 | |||||||
chr9:15435728 | T | TA | 17 | a0001c0001t0002g0226 a0001c0001t0003g0183 a0001c0001t0005g0181 others(14): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.477+2108dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15435728 | ||||||
chr9:15435844 | C | CT | 27 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(24): Show |
31 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.477+2224dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15435844 | ||||||
chr9:15435844 | C | CTT | 31 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0133 others(28): Show |
37 | HG00323.hp1 HG00544.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.477+2223_477+2224d others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15435844 | ||||||
chr9:15435844 | C | CTTT | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(139): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.477+2222_477+2224d others(5): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15435844 | ||||||
chr9:15435844 | C | CTTTT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0086 others(3): Show |
6 | HG00735.hp1 HG02055.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.477+2221_477+2224d others(6): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15435844 | ||||||
chr9:15435937 | A | G | 2 | a0001c0001t0005g0240 a0001c0001t0005g0241 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.477+2301A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435937 | |||||||
chr9:15435969 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(201): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.477+2333A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15435969 | |||||||
chr9:15436030 | G | C | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+2394G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436030 | |||||||
chr9:15436087 | A | G | 1 | a0001c0006t0005g0184 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.477+2451A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436087 | |||||||
chr9:15436189 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.477+2553A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436189 | |||||||
chr9:15436253 | A | G | 8 | a0001c0001t0002g0011 a0001c0001t0002g0026 a0001c0001t0002g0027 others(5): Show |
12 | HG00408.hp1 HG00558.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.477+2617A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436253 | |||||||
chr9:15436500 | C | A | 1 | a0001c0001t0002g0027 | 2 | HG02015.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.477+2864C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436500 | |||||||
chr9:15436755 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.477+3119C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436755 | |||||||
chr9:15436820 | GT | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(169): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.477+3204delT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15436820 | ||||||
chr9:15436820 | GTT | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0149 others(4): Show |
8 | HG01081.hp1 HG01081.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.477+3203_477+3204d others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15436820 | ||||||
chr9:15436832 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.477+3196T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436832 | |||||||
chr9:15436985 | G | A | 2 | a0001c0001t0003g0212 a0001c0001t0021g0213 |
2 | HG01361.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.477+3349G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15436985 | |||||||
chr9:15437064 | A | T | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.477+3428A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437064 | |||||||
chr9:15437165 | C | G | 1 | a0001c0001t0002g0026 | 2 | NA18960.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.477+3529C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437165 | |||||||
chr9:15437379 | C | T | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.477+3743C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437379 | |||||||
chr9:15437475 | C | A | 1 | a0001c0001t0003g0183 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.477+3839C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437475 | |||||||
chr9:15437529 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.477+3893G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437529 | |||||||
chr9:15437605 | C | A | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+3969C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437605 | |||||||
chr9:15437622 | G | GT | 39 | a0001c0001t0001g0049 a0001c0001t0001g0083 a0001c0001t0001g0127 others(36): Show |
44 | HG00544.hp1 HG00735.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.477+4002dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15437622 | ||||||
chr9:15437627 | T | TG | 3 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0006t0005g0184 |
3 | HG02559.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.477+3991_477+3992i others(3): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437627 | |||||||
chr9:15437638 | TG | T | 5 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(2): Show |
7 | HG02109.hp1 HG02280.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.477+4003delG | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437638 | |||||||
chr9:15437639 | G | T | 1 | a0003c0004t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.477+4003G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437639 | |||||||
chr9:15437709 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.477+4073G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437709 | |||||||
chr9:15437727 | C | A | 1 | a0003c0004t0001g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.477+4091C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437727 | |||||||
chr9:15437744 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.477+4108A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437744 | |||||||
chr9:15437846 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.477+4210A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15437846 | |||||||
chr9:15438070 | T | G | 1 | a0001c0001t0001g0019 | 2 | NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.477+4434T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15438070 | |||||||
chr9:15438670 | G | A | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+5034G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15438670 | |||||||
chr9:15438737 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.477+5101A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15438737 | |||||||
chr9:15438857 | C | G | 8 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 others(5): Show |
8 | HG01243.hp2 HG01884.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.477+5221C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15438857 | |||||||
chr9:15438904 | A | T | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.477+5268A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15438904 | |||||||
chr9:15438972 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0059 |
2 | NA18952.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.477+5336A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15438972 | |||||||
chr9:15439159 | G | A | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-5443G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439159 | |||||||
chr9:15439164 | T | C | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-5438T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439164 | |||||||
chr9:15439182 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-5420T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439182 | |||||||
chr9:15439211 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.478-5391G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439211 | |||||||
chr9:15439455 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.478-5147A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439455 | |||||||
chr9:15439655 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.478-4947C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439655 | |||||||
chr9:15439691 | C | T | 2 | a0001c0001t0005g0181 a0001c0001t0005g0182 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.478-4911C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439691 | |||||||
chr9:15439692 | A | T | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-4910A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439692 | |||||||
chr9:15439862 | A | T | 12 | a0001c0001t0004g0007 a0001c0001t0004g0156 a0001c0001t0004g0158 others(9): Show |
14 | HG00544.hp1 HG00735.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-4740A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15439862 | |||||||
chr9:15440253 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.478-4349G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440253 | |||||||
chr9:15440260 | C | A | 2 | a0001c0001t0003g0076 a0001c0001t0003g0091 |
2 | NA19003.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.478-4342C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440260 | |||||||
chr9:15440267 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.478-4335C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440267 | |||||||
chr9:15440477 | G | GT | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-4117dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15440477 | ||||||
chr9:15440503 | A | G | 1 | a0001c0001t0004g0022 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.478-4099A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440503 | |||||||
chr9:15440546 | C | T | 1 | a0001c0001t0002g0026 | 2 | NA18960.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.478-4056C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440546 | |||||||
chr9:15440627 | G | T | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-3975G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440627 | |||||||
chr9:15440677 | C | T | 2 | a0001c0001t0003g0210 a0001c0001t0003g0211 |
2 | HG00438.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.478-3925C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440677 | |||||||
chr9:15440687 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.478-3915C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440687 | |||||||
chr9:15440699 | C | G | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-3903C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440699 | |||||||
chr9:15440819 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(229): Show |
269 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.478-3783A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440819 | |||||||
chr9:15440948 | C | CA | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.478-3635dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15440948 | ||||||
chr9:15440948 | C | CAAAAAA | 7 | a0001c0002t0006g0028 a0001c0002t0006g0030 a0001c0002t0006g0032 others(4): Show |
8 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-3640_478-3635d others(8): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15440948 | ||||||
chr9:15440948 | CA | C | 21 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(18): Show |
24 | HG01069.hp2 HG01074.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.478-3635delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15440948 | ||||||
chr9:15440998 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.478-3604C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15440998 | |||||||
chr9:15441001 | T | A | 1 | a0001c0001t0001g0019 | 2 | NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.478-3601T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441001 | |||||||
chr9:15441156 | T | C | 2 | a0001c0001t0015g0206 a0001c0001t0015g0207 |
2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.478-3446T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441156 | |||||||
chr9:15441187 | C | CT | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
268 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.478-3405dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441187 | ||||||
chr9:15441378 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0004g0022 a0001c0001t0005g0185 a0001c0001t0005g0186 others(1): Show |
5 | HG01074.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-3220_478-3219i others(13): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441378 | ||||||
chr9:15441378 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0005g0187 a0001c0001t0005g0190 a0001c0001t0005g0241 |
3 | HG02723.hp1 HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.478-3220_478-3219i others(14): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441378 | ||||||
chr9:15441378 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0005g0188 a0001c0001t0005g0191 a0001c0001t0005g0192 others(1): Show |
4 | HG02280.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-3220_478-3219i others(15): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441378 | ||||||
chr9:15441378 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0005g0189 a0001c0001t0005g0193 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.478-3220_478-3219i others(16): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441378 | ||||||
chr9:15441378 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0003g0183 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478-3220_478-3219i others(20): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441378 | ||||||
chr9:15441383 | C | CTT | 18 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0093 others(15): Show |
20 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.478-3196_478-3195d others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441383 | ||||||
chr9:15441383 | C | CTTT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
146 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.478-3197_478-3195d others(5): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441383 | ||||||
chr9:15441383 | C | CTTTT | 21 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0049 others(18): Show |
22 | HG00741.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.478-3198_478-3195d others(6): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441383 | ||||||
chr9:15441383 | C | CTTTTT | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0006g0246 others(2): Show |
7 | HG02109.hp1 HG02280.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-3199_478-3195d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441383 | ||||||
chr9:15441383 | C | T | 17 | a0001c0001t0001g0041 a0001c0001t0003g0183 a0001c0001t0004g0022 others(14): Show |
18 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.478-3219C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441383 | |||||||
chr9:15441383 | CTTTTTTT | C | 10 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(7): Show |
12 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.478-3201_478-3195d others(9): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441383 | ||||||
chr9:15441383 | CTTTTTTT others(10): Show |
C | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-3211_478-3195d others(19): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15441383 | ||||||
chr9:15441439 | G | C | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-3163G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441439 | |||||||
chr9:15441650 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.478-2952G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441650 | |||||||
chr9:15441797 | C | T | 1 | a0002c0003t0007g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.478-2805C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441797 | |||||||
chr9:15441856 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.478-2746T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441856 | |||||||
chr9:15441860 | C | T | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-2742C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441860 | |||||||
chr9:15441888 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.478-2714C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441888 | |||||||
chr9:15441924 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(249): Show |
302 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.478-2678T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441924 | |||||||
chr9:15441924 | T | G | 2 | a0001c0001t0001g0122 a0001c0001t0004g0161 |
2 | HG02258.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.478-2678T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15441924 | |||||||
chr9:15442067 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.478-2535C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442067 | |||||||
chr9:15442084 | G | T | 12 | a0001c0001t0004g0007 a0001c0001t0004g0156 a0001c0001t0004g0158 others(9): Show |
14 | HG00544.hp1 HG00735.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-2518G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442084 | |||||||
chr9:15442101 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.478-2501A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442101 | |||||||
chr9:15442120 | C | T | 2 | a0001c0001t0005g0181 a0001c0001t0005g0182 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.478-2482C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442120 | |||||||
chr9:15442129 | G | C | 12 | a0001c0001t0004g0007 a0001c0001t0004g0156 a0001c0001t0004g0158 others(9): Show |
14 | HG00544.hp1 HG00735.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-2473G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442129 | |||||||
chr9:15442139 | G | A | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-2463G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442139 | |||||||
chr9:15442179 | CGGGGCGG others(85): Show |
C | 2 | a0001c0001t0001g0079 a0005c0007t0001g0112 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.478-2381_478-2290d others(94): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15442179 | ||||||
chr9:15442180 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.478-2422G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442180 | |||||||
chr9:15442193 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0156 a0001c0001t0004g0158 others(9): Show |
14 | HG00544.hp1 HG00735.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.478-2409G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442193 | |||||||
chr9:15442226 | G | T | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.478-2376G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442226 | |||||||
chr9:15442238 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.478-2364C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442238 | |||||||
chr9:15442242 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.478-2360C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442242 | |||||||
chr9:15442314 | G | A | 1 | a0001c0001t0004g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.478-2288G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442314 | |||||||
chr9:15442330 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(200): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.478-2272T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442330 | |||||||
chr9:15442357 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.478-2245G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442357 | |||||||
chr9:15442404 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.478-2198A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442404 | |||||||
chr9:15442419 | C | T | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-2183C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442419 | |||||||
chr9:15442426 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.478-2176C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442426 | |||||||
chr9:15442445 | C | T | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-2157C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442445 | |||||||
chr9:15442466 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.478-2136T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442466 | |||||||
chr9:15442493 | AC | A | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-2107delC | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15442493 | ||||||
chr9:15442495 | C | T | 17 | a0001c0001t0001g0123 a0001c0001t0003g0183 a0001c0001t0004g0022 others(14): Show |
18 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.478-2107C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442495 | |||||||
chr9:15442504 | G | A | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-2098G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442504 | |||||||
chr9:15442506 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.478-2096G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442506 | |||||||
chr9:15442605 | A | C | 2 | a0001c0001t0004g0165 a0001c0001t0004g0166 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.478-1997A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442605 | |||||||
chr9:15442609 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(201): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.478-1993A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442609 | |||||||
chr9:15442615 | C | T | 12 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0185 others(9): Show |
13 | HG01074.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-1987C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442615 | |||||||
chr9:15442669 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.478-1933C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442669 | |||||||
chr9:15442724 | C | G | 29 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0003g0005 others(26): Show |
34 | HG00438.hp2 HG00558.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.478-1878C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442724 | |||||||
chr9:15442763 | C | CG | 7 | a0001c0001t0001g0072 a0001c0001t0001g0096 a0001c0001t0001g0153 others(4): Show |
7 | HG01928.hp1 HG01928.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-1835dupG | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 15442763 | ||||||
chr9:15442794 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.478-1808C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442794 | |||||||
chr9:15442847 | C | T | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-1755C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442847 | |||||||
chr9:15442877 | C | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(166): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.478-1725C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442877 | |||||||
chr9:15442906 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.478-1696C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442906 | |||||||
chr9:15442914 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.478-1688A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442914 | |||||||
chr9:15442950 | C | G | 2 | a0001c0001t0002g0222 a0001c0001t0002g0228 |
2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.478-1652C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442950 | |||||||
chr9:15442976 | C | G | 4 | a0002c0003t0007g0167 a0002c0003t0007g0168 a0002c0003t0007g0169 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-1626C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15442976 | |||||||
chr9:15443025 | G | C | 1 | a0001c0001t0001g0019 | 2 | NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.478-1577G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443025 | |||||||
chr9:15443039 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.478-1563C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443039 | |||||||
chr9:15443040 | G | A | 7 | a0001c0001t0005g0187 a0001c0001t0005g0188 a0001c0001t0005g0189 others(4): Show |
7 | HG02280.hp2 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1562G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443040 | |||||||
chr9:15443041 | C | T | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1561C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443041 | |||||||
chr9:15443042 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0022g0216 |
4 | NA18964.hp2 NA18972.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-1560G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443042 | |||||||
chr9:15443047 | C | T | 1 | a0001c0001t0003g0196 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.478-1555C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443047 | |||||||
chr9:15443063 | C | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(161): Show |
190 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.478-1539C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443063 | |||||||
chr9:15443063 | C | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0010 a0001c0001t0003g0076 others(24): Show |
32 | HG00438.hp2 HG00558.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.478-1539C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443063 | |||||||
chr9:15443064 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0228 |
2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.478-1538G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443064 | |||||||
chr9:15443092 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.478-1510G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443092 | |||||||
chr9:15443116 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.478-1486C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443116 | |||||||
chr9:15443193 | G | T | 1 | a0001c0001t0003g0209 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.478-1409G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443193 | |||||||
chr9:15443206 | G | A | 6 | a0001c0001t0001g0245 a0001c0001t0006g0246 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1396G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443206 | |||||||
chr9:15443252 | T | G | 1 | a0001c0001t0004g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.478-1350T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443252 | |||||||
chr9:15443255 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.478-1347G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443255 | |||||||
chr9:15443333 | G | C | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.478-1269G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443333 | |||||||
chr9:15443432 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.478-1170C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443432 | |||||||
chr9:15443543 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.478-1059A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443543 | |||||||
chr9:15443621 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0127 |
2 | HG00673.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.478-981A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443621 | |||||||
chr9:15443660 | C | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.478-942C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443660 | |||||||
chr9:15443765 | C | A | 3 | a0001c0002t0006g0030 a0001c0002t0006g0031 a0001c0002t0006g0032 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.478-837C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443765 | |||||||
chr9:15443921 | G | T | 2 | a0001c0001t0005g0240 a0001c0001t0005g0241 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.478-681G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443921 | |||||||
chr9:15443932 | C | T | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-670C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15443932 | |||||||
chr9:15444029 | T | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0002c0003t0007g0167 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-573T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15444029 | |||||||
chr9:15444320 | C | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.478-282C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15444320 | |||||||
chr9:15444350 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.478-252G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15444350 | |||||||
chr9:15444428 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.478-174T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15444428 | |||||||
chr9:15444441 | T | C | 1 | a0001c0001t0023g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478-161T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 3/8 | chr9 | 15444441 | |||||||
chr9:15444728 | A | G | 1 | a0002c0003t0007g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.582+22A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15444728 | |||||||
chr9:15444909 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.582+203C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15444909 | |||||||
chr9:15445221 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.582+515G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445221 | |||||||
chr9:15445339 | A | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01069.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.582+633A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445339 | |||||||
chr9:15445378 | T | C | 2 | a0001c0001t0005g0240 a0001c0001t0005g0241 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.582+672T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445378 | |||||||
chr9:15445394 | G | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0179 |
3 | HG00642.hp1 HG01081.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.582+688G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445394 | |||||||
chr9:15445413 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.582+707A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445413 | |||||||
chr9:15445568 | AAT | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.582+872_582+873del others(2): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | 15445568 | ||||||
chr9:15445631 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.582+925A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445631 | |||||||
chr9:15445636 | A | AATT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.582+932_582+933ins others(3): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | 15445636 | ||||||
chr9:15445750 | A | G | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.582+1044A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445750 | |||||||
chr9:15445769 | C | A | 2 | a0001c0001t0015g0206 a0001c0001t0015g0207 |
2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.582+1063C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445769 | |||||||
chr9:15445860 | C | T | 1 | a0001c0001t0017g0146 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.582+1154C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445860 | |||||||
chr9:15445938 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.583-1157C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15445938 | |||||||
chr9:15446363 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | NA18982.hp1 NA19003.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.583-732C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15446363 | |||||||
chr9:15446407 | A | G | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.583-688A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15446407 | |||||||
chr9:15446667 | GA | G | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.583-427delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15446667 | |||||||
chr9:15446766 | A | G | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.583-329A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15446766 | |||||||
chr9:15446870 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.583-225A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15446870 | |||||||
chr9:15446879 | G | C | 1 | a0004c0005t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.583-216G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15446879 | |||||||
chr9:15447041 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.583-54G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 4/8 | chr9 | 15447041 | |||||||
chr9:15447363 | A | AACT | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(200): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.732+122_732+124dup others(3): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15447363 | ||||||
chr9:15447495 | T | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.732+251T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15447495 | |||||||
chr9:15447516 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.732+272T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15447516 | |||||||
chr9:15447517 | G | GT | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.732+282dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15447517 | ||||||
chr9:15447517 | G | GTT | 6 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0073 others(3): Show |
6 | HG02145.hp1 HG02683.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+281_732+282dup others(2): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15447517 | ||||||
chr9:15447517 | G | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0135 |
2 | NA18991.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.732+273G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15447517 | |||||||
chr9:15447550 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.732+306G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15447550 | |||||||
chr9:15447584 | C | T | 4 | a0001c0001t0005g0181 a0001c0001t0005g0182 a0001c0001t0005g0240 others(1): Show |
4 | HG02109.hp2 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+340C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15447584 | |||||||
chr9:15447645 | T | C | 3 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0006t0005g0184 |
3 | HG02559.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.732+401T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15447645 | |||||||
chr9:15447716 | T | A | 4 | a0001c0001t0005g0181 a0001c0001t0005g0182 a0001c0001t0005g0240 others(1): Show |
4 | HG02109.hp2 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+472T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15447716 | |||||||
chr9:15448077 | C | A | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.732+833C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448077 | |||||||
chr9:15448308 | A | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG01981.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.732+1064A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448308 | |||||||
chr9:15448335 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0133 |
2 | HG00639.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.732+1091A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448335 | |||||||
chr9:15448387 | GTC | G | 4 | a0001c0001t0005g0181 a0001c0001t0005g0182 a0001c0001t0005g0240 others(1): Show |
4 | HG02109.hp2 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+1147_732+1148d others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15448387 | ||||||
chr9:15448804 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0123 |
2 | NA18991.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.732+1560G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448804 | |||||||
chr9:15448850 | C | G | 1 | a0001c0001t0023g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.732+1606C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448850 | |||||||
chr9:15448872 | C | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0085 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.732+1628C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448872 | |||||||
chr9:15448885 | C | G | 4 | a0003c0004t0001g0012 a0003c0004t0001g0242 a0003c0004t0001g0243 others(1): Show |
6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.732+1641C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448885 | |||||||
chr9:15448950 | C | T | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.732+1706C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15448950 | |||||||
chr9:15449001 | G | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0010 a0001c0001t0003g0076 others(24): Show |
32 | HG00438.hp2 HG00558.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+1757G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449001 | |||||||
chr9:15449044 | A | G | 16 | a0001c0001t0003g0183 a0001c0001t0004g0022 a0001c0001t0005g0181 others(13): Show |
17 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.732+1800A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449044 | |||||||
chr9:15449101 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.732+1857G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449101 | |||||||
chr9:15449164 | G | A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0010 a0001c0001t0003g0076 others(24): Show |
32 | HG00438.hp2 HG00558.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+1920G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449164 | |||||||
chr9:15449305 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0064 a0001c0001t0001g0154 others(1): Show |
4 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-2015G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449305 | |||||||
chr9:15449534 | AT | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0006c0008t0001g0088 |
3 | NA19030.hp2 NA19066.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.733-1784delT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449534 | ||||||
chr9:15449535 | TTA | T | 12 | a0001c0001t0003g0005 a0001c0001t0003g0010 a0001c0001t0003g0091 others(9): Show |
17 | HG00558.hp1 HG01884.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.733-1757_733-1756d others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449535 | ||||||
chr9:15449535 | TTATATAT others(1): Show |
T | 5 | a0001c0001t0005g0181 a0001c0001t0005g0182 a0001c0001t0005g0240 others(2): Show |
5 | HG02109.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-1763_733-1756d others(10): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449535 | ||||||
chr9:15449538 | TATATA | T | 3 | a0003c0004t0001g0012 a0003c0004t0001g0242 a0003c0004t0001g0244 |
5 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-1781_733-1777d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449538 | |||||||
chr9:15449549 | ATATATAT others(11): Show |
A | 1 | a0001c0002t0016g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.733-1769_733-1752d others(20): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449549 | ||||||
chr9:15449551 | ATATATAT others(11): Show |
A | 3 | a0001c0002t0006g0028 a0001c0002t0006g0250 a0001c0002t0006g0251 |
3 | HG01884.hp1 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.733-1767_733-1750d others(20): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449551 | ||||||
chr9:15449551 | ATATATAT others(12): Show |
A | 1 | a0001c0002t0006g0253 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.733-1767_733-1749d others(21): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449551 | ||||||
chr9:15449553 | ATATATAT others(10): Show |
A | 3 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0247 |
4 | HG02258.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-1765_733-1749d others(19): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449553 | ||||||
chr9:15449553 | ATATATAT others(11): Show |
A | 1 | a0001c0002t0006g0252 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.733-1765_733-1748d others(20): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449553 | ||||||
chr9:15449555 | ATATATAT others(12): Show |
A | 2 | a0001c0002t0006g0030 a0001c0002t0006g0032 |
2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.733-1763_733-1745d others(21): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449555 | ||||||
chr9:15449555 | ATATATAT others(13): Show |
A | 1 | a0001c0002t0006g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.733-1763_733-1744d others(22): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449555 | ||||||
chr9:15449557 | A | T | 1 | a0002c0003t0007g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.733-1763A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449557 | |||||||
chr9:15449557 | ATATATAT | A | 9 | a0001c0001t0001g0074 a0001c0001t0004g0007 a0001c0001t0004g0156 others(6): Show |
10 | HG00544.hp1 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.733-1761_733-1755d others(9): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449557 | ||||||
chr9:15449557 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0005g0185 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.733-1761_733-1751d others(13): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449557 | ||||||
chr9:15449558 | TA | T | 3 | a0001c0001t0003g0199 a0001c0001t0003g0204 a0002c0003t0007g0008 |
3 | HG02965.hp2 NA18987.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.733-1761delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449558 | |||||||
chr9:15449558 | TATA | T | 3 | a0001c0001t0003g0076 a0001c0001t0003g0180 a0001c0001t0003g0209 |
3 | HG02083.hp1 HG03710.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.733-1761_733-1759d others(5): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449558 | |||||||
chr9:15449558 | TATATA | T | 6 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0128 others(3): Show |
8 | HG01071.hp1 HG01175.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-1761_733-1757d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449558 | |||||||
chr9:15449559 | A | ATT | 2 | a0001c0001t0002g0025 a0001c0001t0002g0223 |
3 | HG00673.hp1 NA19006.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.733-1760_733-1759i others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449559 | ||||||
chr9:15449559 | A | T | 10 | a0001c0001t0002g0011 a0001c0001t0002g0228 a0001c0001t0003g0005 others(7): Show |
12 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.733-1761A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449559 | |||||||
chr9:15449559 | ATATAT | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0021 others(13): Show |
16 | HG00099.hp2 HG00597.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.733-1759_733-1755d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449559 | ||||||
chr9:15449559 | ATATATT | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0093 others(3): Show |
6 | HG02683.hp1 HG03017.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-1759_733-1754d others(8): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449559 | ||||||
chr9:15449559 | ATATATTT others(5): Show |
A | 1 | a0001c0001t0004g0022 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.733-1759_733-1748d others(14): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449559 | ||||||
chr9:15449560 | TA | T | 6 | a0001c0001t0003g0194 a0001c0001t0003g0195 a0001c0001t0003g0198 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-1759delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449560 | |||||||
chr9:15449561 | A | ATT | 11 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0027 others(8): Show |
12 | HG00558.hp2 HG02015.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.733-1758_733-1757i others(4): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449561 | ||||||
chr9:15449561 | A | T | 26 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(23): Show |
35 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.733-1759A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449561 | |||||||
chr9:15449561 | ATATT | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0053 others(5): Show |
8 | HG01074.hp2 HG01081.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-1757_733-1754d others(6): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449561 | ||||||
chr9:15449561 | ATATTT | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(46): Show |
52 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.733-1757_733-1753d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449561 | ||||||
chr9:15449561 | ATATTTT | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0118 others(4): Show |
7 | HG00639.hp1 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.733-1757_733-1752d others(8): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449561 | ||||||
chr9:15449562 | TA | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0002g0001 others(4): Show |
9 | HG00544.hp2 HG01169.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-1757delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449562 | |||||||
chr9:15449563 | A | T | 62 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0023 others(59): Show |
78 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.733-1757A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449563 | |||||||
chr9:15449563 | AT | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(10): Show |
13 | HG00438.hp1 HG01069.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.733-1733delT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449563 | ||||||
chr9:15449563 | ATTT | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(14): Show |
20 | HG00408.hp2 HG02055.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.733-1735_733-1733d others(5): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449563 | ||||||
chr9:15449563 | ATTTT | A | 9 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0073 others(6): Show |
9 | HG00639.hp2 HG01256.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.733-1736_733-1733d others(6): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449563 | ||||||
chr9:15449563 | ATTTTT | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0020 others(9): Show |
14 | HG00741.hp1 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.733-1737_733-1733d others(7): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 15449563 | ||||||
chr9:15449565 | T | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0087 others(1): Show |
4 | HG01433.hp2 HG02056.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-1755T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449565 | |||||||
chr9:15449566 | T | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0077 others(5): Show |
8 | HG00438.hp1 HG01069.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-1754T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449566 | |||||||
chr9:15449567 | T | A | 2 | a0001c0001t0001g0103 a0001c0001t0019g0137 |
2 | HG02055.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.733-1753T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449567 | |||||||
chr9:15449568 | T | A | 2 | a0001c0001t0001g0034 a0006c0008t0001g0088 |
2 | HG02155.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.733-1752T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449568 | |||||||
chr9:15449569 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.733-1751T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449569 | |||||||
chr9:15449731 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.733-1589C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449731 | |||||||
chr9:15449783 | C | T | 2 | a0001c0001t0005g0240 a0001c0001t0005g0241 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.733-1537C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15449783 | |||||||
chr9:15450401 | T | C | 1 | a0002c0003t0007g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.733-919T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15450401 | |||||||
chr9:15450522 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.733-798G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15450522 | |||||||
chr9:15450742 | G | A | 4 | a0003c0004t0001g0012 a0003c0004t0001g0242 a0003c0004t0001g0243 others(1): Show |
6 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-578G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15450742 | |||||||
chr9:15451055 | A | G | 2 | a0001c0001t0003g0076 a0001c0001t0003g0091 |
2 | NA19003.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.733-265A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15451055 | |||||||
chr9:15451175 | G | A | 10 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(7): Show |
12 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.733-145G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15451175 | |||||||
chr9:15451178 | A | G | 1 | a0001c0001t0004g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.733-142A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15451178 | |||||||
chr9:15451209 | T | TG | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.733-111_733-110ins others(1): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 5/8 | chr9 | 15451209 | |||||||
chr9:15451503 | C | T | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.815+101C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451503 | |||||||
chr9:15451579 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG01433.hp2 HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.815+177C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451579 | |||||||
chr9:15451599 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.815+197G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451599 | |||||||
chr9:15451678 | T | G | 1 | a0001c0001t0008g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.815+276T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451678 | |||||||
chr9:15451807 | C | G | 3 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0006t0005g0184 |
3 | HG02559.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.815+405C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451807 | |||||||
chr9:15451823 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.815+421T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451823 | |||||||
chr9:15451868 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.815+466A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451868 | |||||||
chr9:15451911 | T | G | 5 | a0001c0002t0006g0250 a0001c0002t0006g0251 a0001c0002t0006g0252 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+509T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451911 | |||||||
chr9:15451913 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.815+511A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451913 | |||||||
chr9:15451937 | G | C | 5 | a0001c0001t0001g0245 a0003c0004t0001g0012 a0003c0004t0001g0242 others(2): Show |
7 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.815+535G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451937 | |||||||
chr9:15451957 | T | C | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.815+555T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451957 | |||||||
chr9:15451970 | TA | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.815+580delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 15451970 | ||||||
chr9:15451972 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.815+570A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15451972 | |||||||
chr9:15452126 | C | A | 15 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.815+724C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452126 | |||||||
chr9:15452177 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.815+775G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452177 | |||||||
chr9:15452205 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.815+803C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452205 | |||||||
chr9:15452215 | G | A | 11 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(8): Show |
13 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.815+813G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452215 | |||||||
chr9:15452322 | A | AT | 111 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0014 others(108): Show |
128 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.816-704dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 15452322 | ||||||
chr9:15452322 | A | ATT | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(68): Show |
84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.816-705_816-704dup others(2): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 15452322 | ||||||
chr9:15452322 | A | ATTT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0072 a0001c0001t0001g0117 others(3): Show |
6 | HG00673.hp2 HG01928.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.816-706_816-704dup others(3): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 15452322 | ||||||
chr9:15452375 | A | G | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | NA18942.hp2 NA18960.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816-666A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452375 | |||||||
chr9:15452381 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.816-660C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452381 | |||||||
chr9:15452561 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.816-480G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452561 | |||||||
chr9:15452653 | C | T | 2 | a0001c0001t0005g0191 a0001c0001t0005g0192 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.816-388C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452653 | |||||||
chr9:15452682 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.816-359C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452682 | |||||||
chr9:15452798 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.816-243C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 6/8 | chr9 | 15452798 | |||||||
chr9:15453341 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.980+136T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15453341 | |||||||
chr9:15453359 | C | G | 1 | a0001c0002t0016g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.980+154C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15453359 | |||||||
chr9:15453517 | T | C | 2 | a0001c0001t0010g0157 a0001c0001t0010g0159 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.980+312T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15453517 | |||||||
chr9:15453708 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.980+503T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15453708 | |||||||
chr9:15453799 | G | A | 1 | a0001c0001t0003g0196 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.980+594G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15453799 | |||||||
chr9:15454007 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(147): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.980+802A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454007 | |||||||
chr9:15454052 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.980+847T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454052 | |||||||
chr9:15454080 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.980+875A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454080 | |||||||
chr9:15454113 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.980+908A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454113 | |||||||
chr9:15454167 | C | G | 3 | a0001c0001t0004g0004 a0001c0001t0009g0004 a0001c0001t0009g0172 |
5 | HG02922.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+962C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454167 | |||||||
chr9:15454229 | C | CA | 32 | a0001c0001t0001g0099 a0001c0001t0001g0115 a0001c0001t0002g0205 others(29): Show |
37 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.980+1038dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 15454229 | ||||||
chr9:15454229 | CA | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0149 a0001c0001t0001g0152 others(4): Show |
7 | HG00558.hp2 HG02723.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+1038delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 15454229 | ||||||
chr9:15454363 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.980+1158A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454363 | |||||||
chr9:15454570 | G | A | 6 | a0001c0001t0001g0245 a0002c0003t0007g0171 a0003c0004t0001g0012 others(3): Show |
8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.980+1365G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454570 | |||||||
chr9:15454742 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.980+1537G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454742 | |||||||
chr9:15454754 | A | G | 3 | a0001c0002t0006g0251 a0001c0002t0006g0252 a0001c0002t0006g0253 |
3 | HG01884.hp1 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.980+1549A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454754 | |||||||
chr9:15454818 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.980+1613T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454818 | |||||||
chr9:15454871 | A | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(229): Show |
269 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.980+1666A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454871 | |||||||
chr9:15454873 | G | A | 5 | a0001c0001t0001g0245 a0003c0004t0001g0012 a0003c0004t0001g0242 others(2): Show |
7 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+1668G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454873 | |||||||
chr9:15454888 | C | T | 7 | a0001c0001t0005g0181 a0001c0001t0005g0182 a0001c0001t0005g0185 others(4): Show |
7 | HG01074.hp1 HG02109.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+1683C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454888 | |||||||
chr9:15454921 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.980+1716A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15454921 | |||||||
chr9:15455104 | G | T | 3 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0006t0005g0184 |
3 | HG02559.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.980+1899G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15455104 | |||||||
chr9:15455498 | C | T | 2 | a0001c0001t0005g0181 a0001c0001t0005g0182 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.980+2293C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15455498 | |||||||
chr9:15455569 | GA | G | 5 | a0001c0001t0001g0245 a0003c0004t0001g0012 a0003c0004t0001g0242 others(2): Show |
7 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+2374delA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 15455569 | ||||||
chr9:15455775 | C | T | 1 | a0001c0001t0001g0019 | 2 | NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.981-2185C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15455775 | |||||||
chr9:15455803 | A | G | 1 | a0001c0002t0006g0253 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.981-2157A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15455803 | |||||||
chr9:15455845 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | NA18982.hp1 NA19003.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.981-2115C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15455845 | |||||||
chr9:15455919 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.981-2041A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15455919 | |||||||
chr9:15455922 | T | G | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.981-2038T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15455922 | |||||||
chr9:15455988 | C | CCTCA | 15 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-1971_981-1968d others(6): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 15455988 | ||||||
chr9:15456036 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(200): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.981-1924A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456036 | |||||||
chr9:15456101 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.981-1859C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456101 | |||||||
chr9:15456153 | C | T | 10 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(7): Show |
12 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.981-1807C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456153 | |||||||
chr9:15456178 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.981-1782T>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456178 | |||||||
chr9:15456209 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.981-1751C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456209 | |||||||
chr9:15456239 | A | G | 11 | a0001c0001t0003g0183 a0001c0001t0005g0185 a0001c0001t0005g0186 others(8): Show |
11 | HG01074.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.981-1721A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456239 | |||||||
chr9:15456319 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.981-1641C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456319 | |||||||
chr9:15456373 | G | A | 1 | a0001c0001t0015g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.981-1587G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456373 | |||||||
chr9:15456391 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.981-1569A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456391 | |||||||
chr9:15456427 | A | G | 10 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(7): Show |
12 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.981-1533A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456427 | |||||||
chr9:15456429 | G | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0059 |
2 | NA18952.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.981-1531G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456429 | |||||||
chr9:15456451 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.981-1509C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456451 | |||||||
chr9:15456523 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.981-1437A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456523 | |||||||
chr9:15456606 | T | A | 1 | a0001c0001t0003g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.981-1354T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456606 | |||||||
chr9:15456621 | C | A | 1 | a0001c0001t0002g0226 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.981-1339C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456621 | |||||||
chr9:15456625 | G | T | 6 | a0002c0003t0007g0008 a0002c0003t0007g0167 a0002c0003t0007g0168 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.981-1335G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456625 | |||||||
chr9:15456683 | G | C | 15 | a0001c0001t0003g0183 a0001c0001t0005g0181 a0001c0001t0005g0182 others(12): Show |
15 | HG01074.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-1277G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456683 | |||||||
chr9:15456830 | C | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.981-1130C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456830 | |||||||
chr9:15456989 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.981-971G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15456989 | |||||||
chr9:15457778 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.981-182A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457778 | |||||||
chr9:15457779 | G | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.981-181G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457779 | |||||||
chr9:15457786 | G | A | 1 | a0001c0001t0023g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.981-174G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457786 | |||||||
chr9:15457803 | G | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.981-157G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457803 | |||||||
chr9:15457807 | C | G | 1 | a0001c0001t0004g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.981-153C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457807 | |||||||
chr9:15457855 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(200): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.981-105G>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457855 | |||||||
chr9:15457891 | T | TA | 4 | a0001c0001t0005g0187 a0001c0001t0005g0188 a0001c0001t0005g0189 others(1): Show |
4 | HG02280.hp2 HG02895.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.981-67dupA | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 15457891 | ||||||
chr9:15457895 | A | T | 4 | a0001c0001t0005g0187 a0001c0001t0005g0188 a0001c0001t0005g0189 others(1): Show |
4 | HG02280.hp2 HG02895.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.981-65A>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457895 | |||||||
chr9:15457935 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0116 |
2 | NA19009.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.981-25A>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457935 | |||||||
chr9:15457945 | T | A | 1 | a0001c0001t0018g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.981-15T>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 7/8 | chr9 | 15457945 | |||||||
chr9:15458082 | A | AT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(153): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1088+26dupT | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 15458082 | ||||||
chr9:15458082 | A | ATT | 15 | a0001c0001t0004g0007 a0001c0001t0004g0022 a0001c0001t0004g0156 others(12): Show |
20 | HG00544.hp1 HG00735.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1088+25_1088+26dup others(2): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 15458082 | ||||||
chr9:15458082 | A | ATTT | 6 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0002c0003t0007g0167 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+24_1088+26dup others(3): Show |
SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 15458082 | ||||||
chr9:15458184 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1088+117C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15458184 | |||||||
chr9:15458255 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1088+188T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15458255 | |||||||
chr9:15458569 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1088+502T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15458569 | |||||||
chr9:15458681 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1088+614C>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15458681 | |||||||
chr9:15458893 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1088+826C>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15458893 | |||||||
chr9:15458900 | G | T | 9 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0030 others(6): Show |
11 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1089-819G>T | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15458900 | |||||||
chr9:15458923 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.1089-796T>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15458923 | |||||||
chr9:15459253 | C | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1089-466C>A | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15459253 | |||||||
chr9:15459374 | G | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0223 |
3 | HG00673.hp1 NA19006.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1089-345G>C | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15459374 | |||||||
chr9:15459447 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1089-272A>G | SNAPC3 | ENSG00000164975.16 | transcript | ENST00000380821.8 | protein_coding | 8/8 | chr9 | 15459447 |