Item | Value |
---|---|
geneid | 644815 |
ensemblid | ENSG00000188522.16 |
hgncid | 32554 |
symbol | FAM83G |
name | family with sequence similarity 83 member G |
refseq_nuc | NM_001039999.3 |
refseq_prot | NP_001035088.2 |
ensembl_nuc | ENST00000388995.11 |
ensembl_prot | ENSP00000373647.5 |
mane_status | MANE Select |
chr | chr17 |
start | 18968789 |
end | 19004764 |
strand | - |
ver | v1.2 |
region | chr17:18968789-19004764 |
region5000 | chr17:18963789-19009764 |
regionname0 | FAM83G_chr17_18968789_19004764 |
regionname5000 | FAM83G_chr17_18963789_19009764 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 824 | 166 | 31 | 35 | 66 | 9 | 24 | 49 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0002 | 1/0 | 823 | 93 | 28 | 19 | 33 | 4 | 8 | 28 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(818): Show |
chr17 | 18963789 | 19009764 |
a0003 | 0/0 | 824 | 71 | 20 | 8 | 33 | 1 | 9 | 26 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0004 | 0/0 | 823 | 35 | 6 | 2 | 23 | 0 | 4 | 13 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(818): Show |
chr17 | 18963789 | 19009764 |
a0005 | 0/0 | 823 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(818): Show |
chr17 | 18963789 | 19009764 |
a0006 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0007 | 0/0 | 823 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(818): Show |
chr17 | 18963789 | 19009764 |
a0008 | 0/0 | 823 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(818): Show |
chr17 | 18963789 | 19009764 |
a0009 | 0/0 | 824 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0010 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0011 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0012 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0013 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
a0014 | 0/0 | 824 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | MAFSQ others(819): Show |
chr17 | 18963789 | 19009764 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2472 | 146 | 29 | 35 | 48 | 9 | 24 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0001c0005 | 0/0 | 2472 | 17 | 0 | 0 | 17 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0001c0019 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0001c0022 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0001c0024 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0002c0002 | 1/0 | 2469 | 88 | 23 | 19 | 33 | 4 | 8 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0002c0009 | 0/0 | 2469 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0002c0012 | 0/0 | 2469 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0003c0003 | 0/0 | 2472 | 63 | 18 | 7 | 29 | 1 | 8 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0003c0007 | 0/0 | 2472 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0003c0011 | 0/0 | 2472 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0003c0015 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0003c0016 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0004c0004 | 0/0 | 2469 | 28 | 2 | 1 | 21 | 0 | 4 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0004c0006 | 0/0 | 2469 | 5 | 4 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0004c0010 | 0/0 | 2469 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0005c0008 | 0/0 | 2469 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0006c0014 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0007c0020 | 0/0 | 2469 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0008c0026 | 0/0 | 2469 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2464): Show |
chr17 | 18963789 | 19009764 | ||
a0009c0013 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0010c0017 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0011c0023 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0012c0018 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0013c0025 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 | ||
a0014c0021 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | ATGGC others(2467): Show |
chr17 | 18963789 | 19009764 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5229 | 98 | 14 | 28 | 34 | 5 | 17 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0002 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0003 | 0/0 | 5229 | 27 | 5 | 4 | 8 | 4 | 6 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0004 | 0/0 | 5226 | 6 | 5 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0007 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0008 | 0/0 | 5229 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0009 | 0/1 | 5229 | 3 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0011 | 0/0 | 5229 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0013 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0016 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0017 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0021 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0001t0023 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0005t0001 | 0/0 | 5229 | 17 | 0 | 0 | 17 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0019t0001 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0022t0002 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0001c0024t0010 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0002c0002t0001 | 0/0 | 5226 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0002c0002t0002 | 1/0 | 5226 | 83 | 22 | 18 | 31 | 4 | 7 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0002c0002t0020 | 0/0 | 5226 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0002c0002t0022 | 0/0 | 5212 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5207): Show |
chr17 | 18963789 | 19009764 |
a0002c0002t0024 | 0/0 | 5226 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0002c0002t0025 | 0/0 | 5226 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0002c0009t0002 | 0/0 | 5226 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0002c0012t0001 | 0/0 | 5226 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0002c0012t0006 | 0/0 | 5226 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0001 | 0/0 | 5229 | 45 | 9 | 5 | 25 | 1 | 5 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0003 | 0/0 | 5229 | 5 | 0 | 1 | 3 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0004 | 0/0 | 5226 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0007 | 0/0 | 5229 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0012 | 0/0 | 5229 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0014 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0018 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0019 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0003t0026 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0007t0001 | 0/0 | 5229 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0007t0003 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0011t0010 | 0/0 | 5229 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0015t0003 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0003c0016t0003 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0004c0004t0001 | 0/0 | 5226 | 4 | 0 | 0 | 3 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0004c0004t0002 | 0/0 | 5226 | 16 | 2 | 1 | 12 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0004c0004t0005 | 0/0 | 5226 | 6 | 0 | 0 | 5 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0004c0004t0015 | 0/0 | 5226 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0004c0004t0027 | 0/0 | 5226 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0004c0006t0001 | 0/0 | 5226 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0004c0006t0006 | 0/0 | 5226 | 4 | 3 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0004c0010t0002 | 0/0 | 5226 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0005c0008t0002 | 0/0 | 5226 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0006c0014t0003 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0007c0020t0002 | 0/0 | 5226 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0008c0026t0002 | 0/0 | 5226 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5221): Show |
chr17 | 18963789 | 19009764 |
a0009c0013t0003 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0010c0017t0001 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0011c0023t0003 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0012c0018t0001 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0013c0025t0001 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
a0014c0021t0028 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | CTCGC others(5224): Show |
chr17 | 18963789 | 19009764 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 5 | 2 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 3 | 2 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0008g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0009g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0011g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0016g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0017g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0021g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0001t0023g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0019t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0022t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0001c0024t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0005 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0009 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0014 | 1/0 | 3 | 0 | 1 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0020g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0022g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0024g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0002t0025g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0009t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0012t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0002c0012t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0012g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0018g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0019g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0003t0026g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0007t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0007t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0007t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0011t0010g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0015t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0003c0016t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0015g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0004t0027g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0006t0006g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0010t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0004c0010t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0005c0008t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0005c0008t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0006c0014t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0007c0020t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0008c0026t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0009c0013t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0010c0017t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0011c0023t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0012c0018t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0013c0025t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
a0014c0021t0028g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0249 | EUR | FIN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00408 | hp1 | a0001 | c0005 | t0001 | g0142 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00408 | hp2 | a0001 | c0022 | t0002 | g0195 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00423 | hp1 | a0004 | c0010 | t0002 | g0284 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00544 | hp2 | a0005 | c0008 | t0002 | g0019 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00558 | hp1 | a0005 | c0008 | t0002 | g0019 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00597 | hp1 | a0006 | c0014 | t0003 | g0271 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00609 | hp1 | a0004 | c0004 | t0002 | g0173 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00621 | hp1 | a0003 | c0003 | t0003 | g0039 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00673 | hp1 | a0004 | c0010 | t0002 | g0283 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | CHS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0240 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00738 | hp1 | a0003 | c0003 | t0026 | g0182 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00741 | hp1 | a0003 | c0011 | t0010 | g0029 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0095 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01070 | hp1 | a0004 | c0004 | t0002 | g0161 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01106 | hp2 | a0003 | c0003 | t0001 | g0169 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01109 | hp2 | a0003 | c0003 | t0003 | g0160 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01169 | hp2 | a0002 | c0002 | t0022 | g0228 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01192 | hp1 | a0004 | c0006 | t0006 | g0012 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0241 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01358 | hp1 | a0003 | c0003 | t0001 | g0017 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01496 | hp1 | a0001 | c0001 | t0011 | g0232 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | IBS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0235 | EUR | IBS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | IBS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | IBS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0231 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01891 | hp2 | a0002 | c0009 | t0002 | g0013 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01934 | hp2 | a0003 | c0003 | t0001 | g0157 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0123 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01952 | hp2 | a0001 | c0001 | t0023 | g0099 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01981 | hp1 | a0003 | c0003 | t0001 | g0017 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02015 | hp2 | a0001 | c0001 | t0017 | g0104 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02056 | hp1 | a0004 | c0004 | t0002 | g0262 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02056 | hp2 | a0001 | c0005 | t0001 | g0115 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02071 | hp1 | a0004 | c0004 | t0001 | g0181 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02071 | hp2 | a0003 | c0003 | t0001 | g0291 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02080 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02132 | hp2 | a0004 | c0004 | t0002 | g0261 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02135 | hp1 | a0004 | c0004 | t0027 | g0286 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02155 | hp2 | a0004 | c0004 | t0002 | g0167 | EAS | CDX | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0170 | EAS | CDX | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | CDX | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02257 | hp2 | a0002 | c0009 | t0002 | g0013 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0215 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0163 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02273 | hp1 | a0003 | c0003 | t0001 | g0255 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02300 | hp1 | a0008 | c0026 | t0002 | g0150 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0069 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02622 | hp1 | a0003 | c0003 | t0004 | g0159 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02622 | hp2 | a0002 | c0012 | t0006 | g0056 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02630 | hp1 | a0004 | c0004 | t0002 | g0156 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0204 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02683 | hp2 | a0003 | c0003 | t0019 | g0270 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0221 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02723 | hp1 | a0001 | c0024 | t0010 | g0078 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0290 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0218 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02809 | hp2 | a0002 | c0002 | t0024 | g0191 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02886 | hp2 | a0003 | c0003 | t0007 | g0219 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02896 | hp2 | a0003 | c0003 | t0007 | g0154 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02897 | hp2 | a0003 | c0003 | t0007 | g0153 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0188 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02965 | hp1 | a0003 | c0003 | t0001 | g0158 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02970 | hp1 | a0003 | c0003 | t0004 | g0027 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03017 | hp2 | a0001 | c0001 | t0011 | g0065 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03041 | hp1 | a0003 | c0016 | t0003 | g0293 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0192 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03130 | hp1 | a0004 | c0006 | t0006 | g0012 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0075 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03139 | hp1 | a0004 | c0006 | t0006 | g0012 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0027 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03225 | hp2 | a0002 | c0009 | t0002 | g0013 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03490 | hp2 | a0002 | c0002 | t0025 | g0046 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0238 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03516 | hp1 | a0004 | c0006 | t0001 | g0155 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03540 | hp1 | a0004 | c0004 | t0002 | g0275 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03579 | hp1 | a0003 | c0003 | t0012 | g0043 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0028 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0265 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0223 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03710 | hp1 | a0003 | c0003 | t0003 | g0287 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03710 | hp2 | a0009 | c0013 | t0003 | g0292 | SAS | PJL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0243 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03831 | hp2 | a0004 | c0004 | t0001 | g0177 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03834 | hp1 | a0004 | c0004 | t0015 | g0282 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03927 | hp2 | a0004 | c0004 | t0005 | g0274 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03942 | hp1 | a0003 | c0015 | t0003 | g0256 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03942 | hp2 | a0003 | c0003 | t0001 | g0281 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04115 | hp1 | a0003 | c0003 | t0018 | g0257 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0288 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0280 | SAS | BEB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04204 | hp2 | a0004 | c0004 | t0002 | g0254 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | YRI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0277 | AFR | YRI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18612 | hp1 | a0004 | c0004 | t0002 | g0171 | EAS | CHB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18612 | hp2 | a0004 | c0004 | t0005 | g0041 | EAS | CHB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18747 | hp1 | a0001 | c0005 | t0001 | g0070 | EAS | CHB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | CHB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0028 | AFR | YRI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18942 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18942 | hp2 | a0004 | c0004 | t0002 | g0268 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18945 | hp2 | a0003 | c0003 | t0003 | g0266 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18946 | hp2 | a0001 | c0005 | t0001 | g0090 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18947 | hp1 | a0004 | c0004 | t0002 | g0263 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18948 | hp2 | a0004 | c0004 | t0005 | g0040 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18949 | hp1 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18951 | hp1 | a0003 | c0007 | t0001 | g0164 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18952 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18956 | hp2 | a0010 | c0017 | t0001 | g0260 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18960 | hp1 | a0003 | c0003 | t0001 | g0176 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18960 | hp2 | a0001 | c0005 | t0001 | g0004 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18961 | hp1 | a0004 | c0004 | t0005 | g0294 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18962 | hp1 | a0003 | c0003 | t0014 | g0175 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18964 | hp1 | a0001 | c0005 | t0001 | g0025 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18965 | hp2 | a0003 | c0007 | t0003 | g0186 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18970 | hp1 | a0001 | c0001 | t0021 | g0206 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18970 | hp2 | a0004 | c0004 | t0002 | g0273 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18971 | hp1 | a0001 | c0005 | t0001 | g0004 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18971 | hp2 | a0004 | c0004 | t0001 | g0183 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18975 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18977 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0279 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18979 | hp2 | a0003 | c0007 | t0001 | g0267 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18980 | hp2 | a0001 | c0005 | t0001 | g0108 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18981 | hp1 | a0011 | c0023 | t0003 | g0102 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18981 | hp2 | a0004 | c0004 | t0005 | g0041 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18983 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0285 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18984 | hp2 | a0004 | c0004 | t0002 | g0184 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18985 | hp2 | a0004 | c0004 | t0002 | g0272 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0259 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18986 | hp2 | a0005 | c0008 | t0002 | g0253 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18987 | hp1 | a0004 | c0004 | t0002 | g0185 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18989 | hp1 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18989 | hp2 | a0001 | c0005 | t0001 | g0151 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18992 | hp2 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0258 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18998 | hp1 | a0001 | c0005 | t0001 | g0148 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18999 | hp1 | a0001 | c0001 | t0016 | g0118 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19000 | hp1 | a0001 | c0005 | t0001 | g0025 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19003 | hp2 | a0001 | c0005 | t0001 | g0145 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0168 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19006 | hp1 | a0001 | c0005 | t0001 | g0004 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19009 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19010 | hp2 | a0004 | c0004 | t0005 | g0040 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19011 | hp1 | a0004 | c0004 | t0001 | g0165 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19012 | hp2 | a0012 | c0018 | t0001 | g0087 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | LWK | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19043 | hp1 | a0004 | c0006 | t0006 | g0012 | AFR | LWK | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0113 | AFR | LWK | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19060 | hp1 | a0003 | c0003 | t0003 | g0039 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19060 | hp2 | a0001 | c0005 | t0001 | g0140 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19064 | hp1 | a0005 | c0008 | t0002 | g0019 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19064 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19065 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19070 | hp1 | a0002 | c0002 | t0020 | g0089 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19070 | hp2 | a0001 | c0005 | t0001 | g0045 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19074 | hp1 | a0004 | c0004 | t0002 | g0276 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19080 | hp1 | a0003 | c0007 | t0001 | g0174 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19084 | hp1 | a0001 | c0005 | t0001 | g0004 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19085 | hp1 | a0001 | c0005 | t0001 | g0004 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19087 | hp2 | a0013 | c0025 | t0001 | g0057 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0278 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | YRI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0217 | AFR | YRI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0289 | EUR | TSI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0210 | EUR | TSI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | GIH | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG01123 | hp2 | a0007 | c0020 | t0002 | g0110 | AMR | CLM | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02109 | hp2 | a0001 | c0019 | t0001 | g0072 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | ACB | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0162 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG03471 | hp2 | a0003 | c0003 | t0012 | g0043 | AFR | MSL | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG06807 | hp1 | a0003 | c0011 | t0010 | g0029 | AFR | USA | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
HG06807 | hp2 | a0002 | c0012 | t0001 | g0149 | AFR | USA | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | USA | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | USA | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA21309 | hp1 | a0014 | c0021 | t0028 | g0295 | AFR | LWK | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0211 | AFR | LWK | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0237 | REF | REF | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0014 | REF | REF | FAM83G_chr17_18963789_19009764 | FAM83G | chr17 | 18963789 | 19009764 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18971372 | C | CGGT | 9 | a0001 a0003 a0006 others(6): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
conservative_inframe_insertion | MODERATE | c.2456_2458dupACC | p.Asp819_Arg820insHi others(1): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2642/5226 | 2458/2472 | 820/823 | chr17 | 18971372 | |||
chr17:18971384 | G | A | 1 | a0014 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.2447C>T | p.Ala816Val | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2631/5226 | 2447/2472 | 816/823 | chr17 | 18971384 | |||
chr17:18971652 | C | A | 1 | a0006 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.2179G>T | p.Val727Phe | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2363/5226 | 2179/2472 | 727/823 | chr17 | 18971652 | |||
chr17:18971652 | C | T | 1 | a0007 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2179G>A | p.Val727Ile | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2363/5226 | 2179/2472 | 727/823 | chr17 | 18971652 | |||
chr17:18971694 | C | T | 1 | a0009 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2137G>A | p.Gly713Ser | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2321/5226 | 2137/2472 | 713/823 | chr17 | 18971694 | |||
chr17:18977673 | C | T | 1 | a0005 | 4 | HG00544.hp2 HG00558.hp1 NA18986.hp2 others(1): Show |
missense_variant | MODERATE | c.1993G>A | p.Gly665Ser | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 2177/5226 | 1993/2472 | 665/823 | chr17 | 18977673 | |||
chr17:18977727 | G | A | 1 | a0011 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1939C>T | p.Arg647Trp | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 2123/5226 | 1939/2472 | 647/823 | chr17 | 18977727 | |||
chr17:18978831 | G | A | 1 | a0010 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.835C>T | p.Arg279Trp | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 1019/5226 | 835/2472 | 279/823 | chr17 | 18978831 | |||
chr17:18988318 | C | T | 1 | a0012 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.619G>A | p.Val207Met | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/6 | 803/5226 | 619/2472 | 207/823 | chr17 | 18988318 | |||
chr17:18988386 | G | C | 1 | a0013 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.551C>G | p.Thr184Ser | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/6 | 735/5226 | 551/2472 | 184/823 | chr17 | 18988386 | |||
chr17:19003716 | A | G | 6 | a0003 a0004 a0005 others(3): Show |
113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
missense_variant | MODERATE | c.326T>C | p.Ile109Thr | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/6 | 510/5226 | 326/2472 | 109/823 | chr17 | 19003716 | |||
chr17:19003785 | G | A | 1 | a0008 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.257C>T | p.Pro86Leu | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/6 | 441/5226 | 257/2472 | 86/823 | chr17 | 19003785 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18971407 | C | G | 18 | a0001c0001 a0001c0005 a0001c0019 others(15): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
synonymous_variant | LOW | c.2424G>C | p.Ser808Ser | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2608/5226 | 2424/2472 | 808/823 | chr17 | 18971407 | |||
chr17:18977629 | C | T | 1 | a0001c0019 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2037G>A | p.Ala679Ala | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 2221/5226 | 2037/2472 | 679/823 | chr17 | 18977629 | |||
chr17:18977959 | C | T | 1 | a0004c0010 | 2 | HG00423.hp1 HG00673.hp1 |
synonymous_variant | LOW | c.1707G>A | p.Gly569Gly | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 1891/5226 | 1707/2472 | 569/823 | chr17 | 18977959 | |||
chr17:18978220 | G | A | 1 | a0003c0015 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1446C>T | p.Ala482Ala | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 1630/5226 | 1446/2472 | 482/823 | chr17 | 18978220 | |||
chr17:18978259 | C | T | 3 | a0001c0005 a0003c0007 a0013c0025 |
22 | HG00408.hp1 HG02056.hp2 NA18747.hp1 others(19): Show |
synonymous_variant | LOW | c.1407G>A | p.Arg469Arg | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 1591/5226 | 1407/2472 | 469/823 | chr17 | 18978259 | |||
chr17:18978370 | G | A | 2 | a0001c0024 a0003c0011 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.1296C>T | p.Ile432Ile | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 1480/5226 | 1296/2472 | 432/823 | chr17 | 18978370 | |||
chr17:18978598 | G | A | 1 | a0003c0016 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1068C>T | p.Ser356Ser | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 1252/5226 | 1068/2472 | 356/823 | chr17 | 18978598 | |||
chr17:18978832 | C | T | 1 | a0002c0009 | 3 | HG01891.hp2 HG02257.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.834G>A | p.Ala278Ala | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/6 | 1018/5226 | 834/2472 | 278/823 | chr17 | 18978832 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18968842 | T | A | 1 | a0004c0004t0005 | 6 | HG03927.hp2 NA18612.hp2 NA18948.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2517A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2517 | chr17 | 18968842 | ||||||
chr17:18968910 | A | C | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 others(3): Show |
17 | HG01433.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2449T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2449 | chr17 | 18968910 | ||||||
chr17:18968930 | GTCTCCCC others(7): Show |
G | 1 | a0002c0002t0022 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2415_*2428delATAA others(10): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2415 | chr17 | 18968930 | ||||||
chr17:18969024 | T | C | 27 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(24): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*2335A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2335 | chr17 | 18969024 | ||||||
chr17:18969066 | G | A | 1 | a0001c0001t0017 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2293C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2293 | chr17 | 18969066 | ||||||
chr17:18969134 | T | C | 1 | a0001c0001t0023 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2225A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2225 | chr17 | 18969134 | ||||||
chr17:18969154 | G | A | 1 | a0002c0002t0024 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2205C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2205 | chr17 | 18969154 | ||||||
chr17:18969190 | G | A | 2 | a0001c0024t0010 a0003c0011t0010 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2169C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2169 | chr17 | 18969190 | ||||||
chr17:18969208 | A | G | 14 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0017 others(11): Show |
49 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2151T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2151 | chr17 | 18969208 | ||||||
chr17:18969268 | C | T | 12 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0017 others(9): Show |
47 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2091G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2091 | chr17 | 18969268 | ||||||
chr17:18969281 | T | C | 1 | a0001c0001t0008 | 3 | NA18952.hp1 NA18983.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2078A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2078 | chr17 | 18969281 | ||||||
chr17:18969286 | G | A | 1 | a0002c0002t0025 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2073C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2073 | chr17 | 18969286 | ||||||
chr17:18969358 | A | C | 1 | a0001c0001t0021 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2001T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 2001 | chr17 | 18969358 | ||||||
chr17:18969408 | T | A | 1 | a0003c0003t0026 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1951A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 1951 | chr17 | 18969408 | ||||||
chr17:18969465 | C | T | 1 | a0004c0004t0027 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1894G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 1894 | chr17 | 18969465 | ||||||
chr17:18969513 | C | T | 1 | a0002c0002t0020 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1846G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 1846 | chr17 | 18969513 | ||||||
chr17:18969641 | G | A | 1 | a0004c0004t0027 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 1718 | chr17 | 18969641 | ||||||
chr17:18969885 | T | C | 1 | a0001c0001t0011 | 2 | HG01496.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1474A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 1474 | chr17 | 18969885 | ||||||
chr17:18970014 | C | T | 1 | a0003c0003t0019 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 1345 | chr17 | 18970014 | ||||||
chr17:18970492 | C | G | 2 | a0001c0024t0010 a0003c0011t0010 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*867G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 867 | chr17 | 18970492 | ||||||
chr17:18970536 | G | C | 12 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0017 others(9): Show |
44 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*823C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 823 | chr17 | 18970536 | ||||||
chr17:18970592 | A | G | 14 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0017 others(11): Show |
49 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*767T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 767 | chr17 | 18970592 | ||||||
chr17:18970696 | C | A | 3 | a0001c0001t0007 a0001c0001t0013 a0003c0003t0007 |
5 | HG02109.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*663G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 663 | chr17 | 18970696 | ||||||
chr17:18970784 | T | G | 2 | a0001c0024t0010 a0003c0011t0010 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*575A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 575 | chr17 | 18970784 | ||||||
chr17:18970836 | TAAA | T | 2 | a0001c0001t0004 a0003c0003t0004 |
10 | HG01433.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*522delTTT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 520 | chr17 | 18970836 | ||||||
chr17:18970900 | A | C | 1 | a0001c0001t0016 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 459 | chr17 | 18970900 | ||||||
chr17:18970952 | G | C | 2 | a0001c0001t0004 a0003c0003t0004 |
10 | HG01433.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*407C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 407 | chr17 | 18970952 | ||||||
chr17:18971008 | T | G | 1 | a0014c0021t0028 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 351 | chr17 | 18971008 | ||||||
chr17:18971056 | C | T | 1 | a0004c0004t0015 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 303 | chr17 | 18971056 | ||||||
chr17:18971116 | C | T | 1 | a0003c0003t0014 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*243G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 243 | chr17 | 18971116 | ||||||
chr17:18971257 | C | T | 1 | a0001c0001t0013 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 6/6 | 102 | chr17 | 18971257 | ||||||
chr17:19004751 | G | A | 1 | a0003c0003t0012 | 2 | HG03471.hp2 HG03579.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-171C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/6 | chr17 | 19004751 | |||||||
chr17:19004753 | C | T | 1 | a0014c0021t0028 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/6 | 712 | chr17 | 19004753 | ||||||
chr17:19004757 | G | A | 1 | a0014c0021t0028 | 1 | NA21309.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-177C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/6 | chr17 | 19004757 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18972005 | A | G | 2 | a0001c0001t0002g0198 a0001c0001t0009g0192 |
2 | HG01884.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2083-257T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972005 | |||||||
chr17:18972342 | T | C | 3 | a0001c0001t0003g0077 a0001c0001t0003g0081 a0003c0003t0003g0160 |
3 | HG01109.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2083-594A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972342 | |||||||
chr17:18972360 | C | T | 1 | a0003c0003t0001g0157 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2083-612G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972360 | |||||||
chr17:18972397 | A | T | 1 | a0001c0001t0003g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2083-649T>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972397 | |||||||
chr17:18972458 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0020 others(91): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2083-710G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972458 | |||||||
chr17:18972651 | A | G | 2 | a0001c0001t0001g0216 a0003c0003t0001g0163 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2083-903T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972651 | |||||||
chr17:18972755 | G | A | 1 | a0001c0001t0003g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2083-1007C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972755 | |||||||
chr17:18972845 | G | A | 2 | a0002c0002t0002g0122 a0002c0002t0002g0137 |
2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2083-1097C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972845 | |||||||
chr17:18972867 | T | TA | 38 | a0001c0001t0003g0003 a0001c0001t0003g0044 a0001c0001t0003g0051 others(35): Show |
45 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.2083-1120dupT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972867 | |||||||
chr17:18972867 | TA | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(132): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.2083-1120delT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18972867 | |||||||
chr17:18973253 | C | T | 4 | a0001c0001t0003g0244 a0001c0001t0003g0245 a0001c0001t0003g0247 others(1): Show |
4 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2083-1505G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973253 | |||||||
chr17:18973283 | A | C | 35 | a0001c0001t0003g0003 a0001c0001t0003g0044 a0001c0001t0003g0051 others(32): Show |
42 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2083-1535T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973283 | |||||||
chr17:18973503 | G | A | 1 | a0003c0003t0001g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2083-1755C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973503 | |||||||
chr17:18973884 | G | GT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(127): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.2083-2137dupA | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973884 | |||||||
chr17:18973884 | G | GTT | 18 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0063 others(15): Show |
20 | HG00408.hp2 HG00735.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.2083-2138_2083-213 others(6): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973884 | |||||||
chr17:18973884 | GT | G | 10 | a0001c0001t0004g0054 a0001c0001t0004g0082 a0001c0001t0004g0133 others(7): Show |
11 | HG01256.hp2 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2083-2137delA | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973884 | |||||||
chr17:18973884 | GTTTTTTT others(1): Show |
G | 32 | a0001c0001t0003g0003 a0001c0001t0003g0044 a0001c0001t0003g0051 others(29): Show |
39 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.2083-2144_2083-213 others(12): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973884 | |||||||
chr17:18973885 | T | G | 1 | a0002c0002t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2083-2137A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973885 | |||||||
chr17:18973906 | T | C | 9 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0082 others(6): Show |
10 | HG01433.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2083-2158A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18973906 | |||||||
chr17:18974037 | C | T | 2 | a0002c0012t0006g0056 a0004c0006t0006g0012 |
5 | HG01192.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2083-2289G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974037 | |||||||
chr17:18974053 | C | T | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2083-2305G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974053 | |||||||
chr17:18974134 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(131): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.2083-2386C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974134 | |||||||
chr17:18974236 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2083-2488C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974236 | |||||||
chr17:18974333 | C | T | 1 | a0004c0004t0005g0294 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2083-2585G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974333 | |||||||
chr17:18974396 | C | T | 2 | a0002c0012t0001g0149 a0004c0006t0001g0155 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2083-2648G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974396 | |||||||
chr17:18974416 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2083-2668G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974416 | |||||||
chr17:18974493 | G | C | 2 | a0002c0012t0006g0056 a0004c0006t0006g0012 |
5 | HG01192.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2083-2745C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974493 | |||||||
chr17:18974555 | G | A | 9 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0082 others(6): Show |
10 | HG01433.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2083-2807C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974555 | |||||||
chr17:18974599 | C | T | 4 | a0001c0001t0003g0051 a0001c0001t0003g0204 a0001c0001t0003g0210 others(1): Show |
4 | HG01361.hp1 HG02683.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.2083-2851G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974599 | |||||||
chr17:18974611 | T | C | 1 | a0003c0003t0001g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2083-2863A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974611 | |||||||
chr17:18974752 | T | G | 1 | a0003c0003t0001g0180 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2082+2832A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974752 | |||||||
chr17:18974824 | G | A | 2 | a0001c0001t0001g0216 a0003c0003t0001g0163 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2082+2760C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18974824 | |||||||
chr17:18975273 | G | T | 2 | a0003c0003t0001g0269 a0003c0003t0001g0285 |
2 | HG00558.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2082+2311C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975273 | |||||||
chr17:18975345 | G | A | 4 | a0001c0001t0009g0192 a0001c0001t0009g0227 a0002c0012t0006g0056 others(1): Show |
7 | HG01192.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2082+2239C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975345 | |||||||
chr17:18975411 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2082+2173G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975411 | |||||||
chr17:18975461 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(148): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2082+2123C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975461 | |||||||
chr17:18975504 | A | C | 1 | a0002c0002t0002g0125 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2082+2080T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975504 | |||||||
chr17:18975509 | G | A | 2 | a0002c0012t0001g0149 a0004c0006t0001g0155 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2082+2075C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975509 | |||||||
chr17:18975532 | A | C | 2 | a0003c0003t0003g0039 a0006c0014t0003g0271 |
3 | HG00597.hp1 HG00621.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2082+2052T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975532 | |||||||
chr17:18975749 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2082+1835A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975749 | |||||||
chr17:18975762 | C | T | 1 | a0014c0021t0028g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2082+1822G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975762 | |||||||
chr17:18975800 | G | A | 16 | a0001c0001t0003g0208 a0001c0001t0004g0054 a0001c0001t0004g0055 others(13): Show |
18 | HG01433.hp2 HG02055.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.2082+1784C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975800 | |||||||
chr17:18975855 | T | C | 2 | a0001c0024t0010g0078 a0003c0011t0010g0029 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2082+1729A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975855 | |||||||
chr17:18975963 | C | T | 1 | a0003c0003t0001g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2082+1621G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18975963 | |||||||
chr17:18976015 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2082+1569C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976015 | |||||||
chr17:18976058 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(188): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2082+1526T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976058 | |||||||
chr17:18976110 | A | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(129): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.2082+1474T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976110 | |||||||
chr17:18976175 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(188): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.2082+1409T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976175 | |||||||
chr17:18976187 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0009g0192 a0002c0012t0006g0056 a0004c0006t0006g0012 |
6 | HG01192.hp1 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2082+1396_2082+139 others(17): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976187 | |||||||
chr17:18976187 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0073 a0001c0001t0001g0239 a0003c0007t0003g0186 others(1): Show |
4 | HG01106.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2082+1396_2082+139 others(18): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976187 | |||||||
chr17:18976187 | C | CAAAAAAA others(8): Show |
129 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(126): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2082+1396_2082+139 others(19): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976187 | |||||||
chr17:18976187 | C | CAAAAAAA others(9): Show |
50 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0020 others(47): Show |
68 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2082+1396_2082+139 others(20): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976187 | |||||||
chr17:18976187 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0003c0003t0001g0281 |
3 | HG03942.hp2 NA18946.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.2082+1396_2082+139 others(21): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976187 | |||||||
chr17:18976191 | A | AG | 2 | a0001c0024t0010g0078 a0003c0011t0010g0029 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2082+1392_2082+139 others(5): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976191 | |||||||
chr17:18976269 | C | T | 1 | a0002c0002t0002g0096 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2082+1315G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976269 | |||||||
chr17:18976280 | C | T | 1 | a0014c0021t0028g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2082+1304G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976280 | |||||||
chr17:18976336 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(123): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.2082+1248G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976336 | |||||||
chr17:18976448 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2082+1136C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976448 | |||||||
chr17:18976605 | T | C | 2 | a0002c0012t0006g0056 a0004c0006t0006g0012 |
5 | HG01192.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2082+979A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976605 | |||||||
chr17:18976693 | C | T | 3 | a0001c0001t0009g0192 a0002c0012t0006g0056 a0004c0006t0006g0012 |
6 | HG01192.hp1 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2082+891G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976693 | |||||||
chr17:18976703 | T | C | 2 | a0001c0001t0009g0227 a0012c0018t0001g0087 |
2 | HG02280.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2082+881A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976703 | |||||||
chr17:18976955 | C | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0020 others(88): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.2082+629G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18976955 | |||||||
chr17:18977226 | C | T | 2 | a0002c0012t0001g0149 a0004c0006t0001g0155 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2082+358G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18977226 | |||||||
chr17:18977227 | G | A | 3 | a0002c0002t0002g0018 a0002c0002t0002g0127 a0002c0002t0002g0135 |
5 | HG00597.hp2 HG02027.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+357C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18977227 | |||||||
chr17:18977348 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(209): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.2082+236A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18977348 | |||||||
chr17:18977423 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2082+161C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18977423 | |||||||
chr17:18977537 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2082+47C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 5/5 | chr17 | 18977537 | |||||||
chr17:18978900 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.816-50G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18978900 | |||||||
chr17:18978901 | G | A | 51 | a0001c0001t0003g0003 a0001c0001t0003g0044 a0001c0001t0003g0051 others(48): Show |
63 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.816-51C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18978901 | |||||||
chr17:18978928 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816-78A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18978928 | |||||||
chr17:18979133 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(211): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.816-283A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979133 | |||||||
chr17:18979189 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.816-339G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979189 | |||||||
chr17:18979282 | C | T | 1 | a0009c0013t0003g0292 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.815+267G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979282 | |||||||
chr17:18979304 | G | A | 1 | a0002c0009t0002g0013 | 3 | HG01891.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.815+245C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979304 | |||||||
chr17:18979330 | C | T | 1 | a0002c0002t0002g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.815+219G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979330 | |||||||
chr17:18979355 | C | T | 2 | a0002c0002t0002g0035 a0004c0004t0002g0156 |
3 | HG02630.hp1 HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.815+194G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979355 | |||||||
chr17:18979397 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.815+152G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979397 | |||||||
chr17:18979515 | T | G | 1 | a0002c0002t0002g0103 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.815+34A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 4/5 | chr17 | 18979515 | |||||||
chr17:18979678 | T | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(290): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
splice_region_variant&intron_variant | LOW | c.691-5A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18979678 | |||||||
chr17:18979777 | G | A | 1 | a0001c0005t0001g0025 | 2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.691-104C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18979777 | |||||||
chr17:18979905 | G | A | 2 | a0001c0024t0010g0078 a0003c0011t0010g0029 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.691-232C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18979905 | |||||||
chr17:18979990 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-317T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18979990 | |||||||
chr17:18979991 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-318C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18979991 | |||||||
chr17:18979992 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-319G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18979992 | |||||||
chr17:18980027 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-354C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980027 | |||||||
chr17:18980028 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-355A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980028 | |||||||
chr17:18980179 | G | A | 2 | a0001c0024t0010g0078 a0003c0011t0010g0029 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.691-506C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980179 | |||||||
chr17:18980190 | C | T | 1 | a0005c0008t0002g0253 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.691-517G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980190 | |||||||
chr17:18980346 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.691-673G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980346 | |||||||
chr17:18980376 | G | A | 2 | a0001c0024t0010g0078 a0003c0011t0010g0029 |
3 | HG00741.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.691-703C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980376 | |||||||
chr17:18980441 | A | G | 2 | a0002c0012t0001g0149 a0004c0006t0001g0155 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.691-768T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980441 | |||||||
chr17:18980463 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.691-790G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980463 | |||||||
chr17:18980601 | C | G | 2 | a0002c0012t0006g0056 a0004c0006t0006g0012 |
5 | HG01192.hp1 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-928G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980601 | |||||||
chr17:18980841 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0128 |
2 | NA18964.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.691-1168G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980841 | |||||||
chr17:18980945 | C | G | 1 | a0003c0007t0003g0186 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.691-1272G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18980945 | |||||||
chr17:18981035 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-1362A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981035 | |||||||
chr17:18981276 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.691-1603G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981276 | |||||||
chr17:18981557 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.691-1884C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981557 | |||||||
chr17:18981576 | T | C | 3 | a0001c0001t0002g0198 a0001c0001t0009g0192 a0003c0003t0001g0163 |
3 | HG01884.hp1 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.691-1903A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981576 | |||||||
chr17:18981612 | G | T | 1 | a0003c0003t0001g0255 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.691-1939C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981612 | |||||||
chr17:18981616 | G | T | 1 | a0003c0003t0001g0255 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.691-1943C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981616 | |||||||
chr17:18981702 | C | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(290): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.691-2029G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981702 | |||||||
chr17:18981766 | C | A | 1 | a0001c0001t0017g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.691-2093G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981766 | |||||||
chr17:18981774 | C | G | 1 | a0001c0001t0004g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.691-2101G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981774 | |||||||
chr17:18981828 | G | A | 3 | a0002c0002t0002g0049 a0002c0002t0002g0050 a0002c0002t0002g0235 |
3 | HG01256.hp2 HG01258.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.691-2155C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981828 | |||||||
chr17:18981874 | C | T | 2 | a0001c0001t0002g0198 a0003c0003t0001g0163 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.691-2201G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981874 | |||||||
chr17:18981878 | C | T | 1 | a0002c0002t0002g0106 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.691-2205G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18981878 | |||||||
chr17:18982303 | C | T | 3 | a0001c0001t0002g0198 a0003c0003t0001g0163 a0003c0003t0012g0043 |
4 | HG01884.hp1 HG02258.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-2630G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982303 | |||||||
chr17:18982317 | C | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0242 |
3 | HG01243.hp2 HG01993.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.691-2644G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982317 | |||||||
chr17:18982321 | A | C | 6 | a0002c0002t0002g0127 a0004c0004t0002g0276 a0004c0004t0005g0040 others(3): Show |
8 | HG02027.hp2 HG03927.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-2648T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982321 | |||||||
chr17:18982373 | C | T | 3 | a0001c0001t0002g0198 a0003c0003t0001g0163 a0003c0003t0012g0043 |
4 | HG01884.hp1 HG02258.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-2700G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982373 | |||||||
chr17:18982399 | G | A | 1 | a0002c0012t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.691-2726C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982399 | |||||||
chr17:18982602 | T | C | 14 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0059 others(11): Show |
15 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-2929A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982602 | |||||||
chr17:18982623 | C | T | 3 | a0001c0001t0002g0198 a0003c0003t0001g0163 a0003c0003t0012g0043 |
4 | HG01884.hp1 HG02258.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-2950G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982623 | |||||||
chr17:18982824 | A | G | 3 | a0001c0001t0002g0198 a0003c0003t0001g0163 a0003c0003t0012g0043 |
4 | HG01884.hp1 HG02258.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-3151T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982824 | |||||||
chr17:18982878 | G | A | 3 | a0001c0001t0002g0198 a0003c0003t0001g0163 a0003c0003t0012g0043 |
4 | HG01884.hp1 HG02258.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-3205C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982878 | |||||||
chr17:18982968 | C | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0084 others(19): Show |
33 | HG01891.hp2 HG02004.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.691-3295G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18982968 | |||||||
chr17:18983078 | A | C | 1 | a0002c0012t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.691-3405T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983078 | |||||||
chr17:18983117 | G | A | 1 | a0003c0003t0001g0255 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.691-3444C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983117 | |||||||
chr17:18983274 | C | G | 3 | a0001c0001t0002g0198 a0003c0003t0001g0163 a0003c0003t0012g0043 |
4 | HG01884.hp1 HG02258.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-3601G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983274 | |||||||
chr17:18983305 | G | A | 1 | a0003c0003t0001g0180 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.691-3632C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983305 | |||||||
chr17:18983484 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.691-3811A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983484 | |||||||
chr17:18983536 | T | C | 19 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
20 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.691-3863A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983536 | |||||||
chr17:18983609 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.691-3936G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983609 | |||||||
chr17:18983824 | G | A | 1 | a0001c0001t0001g0010 | 4 | HG02004.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-4151C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983824 | |||||||
chr17:18983929 | G | A | 6 | a0001c0001t0007g0066 a0001c0001t0009g0192 a0003c0003t0007g0153 others(3): Show |
6 | HG02109.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-4256C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983929 | |||||||
chr17:18983939 | G | A | 1 | a0001c0001t0009g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.691-4266C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18983939 | |||||||
chr17:18984010 | C | T | 12 | a0001c0001t0001g0076 a0001c0001t0003g0187 a0001c0001t0004g0190 others(9): Show |
17 | HG01433.hp2 HG02055.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.690+4237G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984010 | |||||||
chr17:18984065 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.690+4182C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984065 | |||||||
chr17:18984159 | G | A | 2 | a0003c0003t0001g0152 a0003c0003t0001g0166 |
2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.690+4088C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984159 | |||||||
chr17:18984170 | A | G | 2 | a0003c0003t0003g0039 a0006c0014t0003g0271 |
3 | HG00597.hp1 HG00621.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.690+4077T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984170 | |||||||
chr17:18984202 | C | G | 1 | a0001c0005t0001g0145 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.690+4045G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984202 | |||||||
chr17:18984267 | G | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG02647.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+3980C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984267 | |||||||
chr17:18984290 | G | A | 1 | a0002c0012t0006g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.690+3957C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984290 | |||||||
chr17:18984332 | C | CA | 18 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0105 others(15): Show |
19 | HG00544.hp1 HG01070.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.690+3914dupT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984332 | |||||||
chr17:18984332 | C | CAA | 69 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(66): Show |
90 | HG00280.hp1 HG00609.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.690+3913_690+3914d others(4): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984332 | |||||||
chr17:18984332 | C | CAAA | 3 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0001g0209 |
6 | HG02004.hp2 HG02027.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.690+3912_690+3914d others(5): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984332 | |||||||
chr17:18984383 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(284): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.690+3864G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984383 | |||||||
chr17:18984470 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.690+3777G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984470 | |||||||
chr17:18984484 | G | A | 3 | a0002c0002t0002g0201 a0003c0003t0001g0280 a0003c0003t0001g0281 |
3 | HG01257.hp2 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.690+3763C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984484 | |||||||
chr17:18984509 | C | G | 1 | a0003c0003t0001g0158 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.690+3738G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984509 | |||||||
chr17:18984829 | G | A | 1 | a0014c0021t0028g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.690+3418C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984829 | |||||||
chr17:18984907 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.690+3340G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984907 | |||||||
chr17:18984929 | C | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+3318G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984929 | |||||||
chr17:18984932 | G | A | 1 | a0003c0003t0001g0168 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.690+3315C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984932 | |||||||
chr17:18984979 | C | G | 1 | a0002c0002t0025g0046 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.690+3268G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18984979 | |||||||
chr17:18985050 | A | C | 1 | a0004c0004t0005g0294 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.690+3197T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985050 | |||||||
chr17:18985395 | A | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0064 |
4 | NA18948.hp1 NA18985.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+2852T>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985395 | |||||||
chr17:18985435 | T | C | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(7): Show |
12 | HG00741.hp1 HG01070.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.690+2812A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985435 | |||||||
chr17:18985467 | G | A | 2 | a0001c0001t0002g0198 a0003c0003t0001g0163 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.690+2780C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985467 | |||||||
chr17:18985572 | G | A | 4 | a0002c0002t0002g0146 a0004c0004t0002g0184 a0004c0004t0002g0185 others(1): Show |
4 | NA18947.hp1 NA18984.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+2675C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985572 | |||||||
chr17:18985601 | C | T | 1 | a0003c0003t0001g0264 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.690+2646G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985601 | |||||||
chr17:18985744 | A | G | 6 | a0001c0001t0007g0066 a0001c0001t0009g0192 a0003c0003t0007g0153 others(3): Show |
6 | HG02109.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+2503T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985744 | |||||||
chr17:18985931 | T | G | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+2316A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18985931 | |||||||
chr17:18986128 | G | A | 1 | a0001c0001t0003g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.690+2119C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986128 | |||||||
chr17:18986190 | T | G | 1 | a0004c0004t0002g0273 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.690+2057A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986190 | |||||||
chr17:18986402 | T | A | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+1845A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986402 | |||||||
chr17:18986481 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(45): Show |
65 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.690+1766G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986481 | |||||||
chr17:18986484 | C | T | 13 | a0001c0001t0002g0198 a0001c0001t0003g0187 a0001c0001t0004g0190 others(10): Show |
18 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+1763G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986484 | |||||||
chr17:18986516 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+1731C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986516 | |||||||
chr17:18986620 | C | T | 2 | a0002c0002t0002g0241 a0002c0002t0022g0228 |
2 | HG01169.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.690+1627G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986620 | |||||||
chr17:18986636 | T | G | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+1611A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986636 | |||||||
chr17:18986653 | C | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(7): Show |
12 | HG00741.hp1 HG01070.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.690+1594G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986653 | |||||||
chr17:18986917 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.690+1330G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986917 | |||||||
chr17:18986928 | A | G | 1 | a0002c0002t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.690+1319T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986928 | |||||||
chr17:18986938 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0003g0092 a0001c0001t0003g0093 others(1): Show |
4 | NA18946.hp2 NA18955.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+1309G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18986938 | |||||||
chr17:18987086 | C | T | 2 | a0001c0001t0003g0187 a0002c0002t0002g0008 |
5 | HG02717.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+1161G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987086 | |||||||
chr17:18987164 | A | G | 2 | a0002c0002t0002g0088 a0002c0002t0020g0089 |
2 | NA18945.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.690+1083T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987164 | |||||||
chr17:18987340 | G | T | 1 | a0001c0005t0001g0140 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.690+907C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987340 | |||||||
chr17:18987351 | A | G | 1 | a0004c0004t0002g0275 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.690+896T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987351 | |||||||
chr17:18987397 | T | C | 4 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0133 others(1): Show |
4 | HG02630.hp2 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+850A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987397 | |||||||
chr17:18987439 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.690+808G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987439 | |||||||
chr17:18987442 | A | G | 2 | a0002c0002t0002g0127 a0004c0004t0005g0040 |
3 | HG02027.hp2 NA18948.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.690+805T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987442 | |||||||
chr17:18987449 | T | C | 80 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(77): Show |
106 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(103): Show |
intron_variant | MODIFIER | c.690+798A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987449 | |||||||
chr17:18987725 | T | C | 1 | a0002c0002t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.690+522A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18987725 | |||||||
chr17:18988005 | G | T | 68 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(65): Show |
91 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.690+242C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18988005 | |||||||
chr17:18988067 | T | C | 1 | a0002c0002t0002g0131 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.690+180A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18988067 | |||||||
chr17:18988177 | C | T | 1 | a0003c0003t0001g0288 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.690+70G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 3/5 | chr17 | 18988177 | |||||||
chr17:18988461 | G | A | 5 | a0001c0001t0007g0066 a0003c0003t0007g0153 a0003c0003t0007g0154 others(2): Show |
5 | HG02109.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-47C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18988461 | |||||||
chr17:18988695 | T | G | 1 | a0002c0002t0002g0109 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.523-281A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18988695 | |||||||
chr17:18988932 | C | G | 1 | a0003c0003t0001g0172 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.523-518G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18988932 | |||||||
chr17:18989119 | C | T | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.523-705G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989119 | |||||||
chr17:18989331 | C | T | 3 | a0001c0001t0003g0214 a0003c0003t0003g0287 a0003c0003t0019g0270 |
3 | HG02683.hp2 HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.523-917G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989331 | |||||||
chr17:18989343 | G | A | 2 | a0001c0001t0001g0234 a0002c0002t0002g0137 |
2 | HG00280.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.523-929C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989343 | |||||||
chr17:18989450 | C | CCCTACTG others(3): Show |
72 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(69): Show |
96 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(93): Show |
intron_variant | MODIFIER | c.523-1037_523-1036i others(12): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989450 | |||||||
chr17:18989593 | A | G | 1 | a0002c0002t0002g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.523-1179T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989593 | |||||||
chr17:18989769 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.523-1355T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989769 | |||||||
chr17:18989902 | A | C | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(79): Show |
108 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(105): Show |
intron_variant | MODIFIER | c.523-1488T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989902 | |||||||
chr17:18989959 | G | A | 13 | a0001c0001t0002g0198 a0001c0001t0003g0187 a0001c0001t0004g0190 others(10): Show |
18 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-1545C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18989959 | |||||||
chr17:18990201 | C | G | 1 | a0002c0002t0002g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.523-1787G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18990201 | |||||||
chr17:18990253 | G | A | 1 | a0002c0002t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.523-1839C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18990253 | |||||||
chr17:18990303 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.523-1889G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18990303 | |||||||
chr17:18990564 | G | A | 1 | a0003c0003t0001g0170 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.523-2150C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18990564 | |||||||
chr17:18990569 | C | T | 1 | a0001c0022t0002g0195 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.523-2155G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18990569 | |||||||
chr17:18990597 | T | TC | 13 | a0001c0001t0002g0198 a0001c0001t0003g0187 a0001c0001t0004g0190 others(10): Show |
18 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-2184dupG | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18990597 | |||||||
chr17:18990765 | G | A | 1 | a0002c0002t0002g0109 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.523-2351C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18990765 | |||||||
chr17:18991216 | C | T | 1 | a0003c0003t0001g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.523-2802G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991216 | |||||||
chr17:18991283 | C | A | 1 | a0003c0003t0004g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.523-2869G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991283 | |||||||
chr17:18991285 | G | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0084 others(20): Show |
34 | HG01891.hp2 HG02004.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.523-2871C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991285 | |||||||
chr17:18991326 | C | T | 2 | a0001c0001t0003g0214 a0003c0003t0003g0287 |
2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.523-2912G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991326 | |||||||
chr17:18991343 | T | G | 26 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0038 others(23): Show |
32 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.523-2929A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991343 | |||||||
chr17:18991369 | G | A | 1 | a0004c0004t0002g0161 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.523-2955C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991369 | |||||||
chr17:18991405 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.523-2991T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991405 | |||||||
chr17:18991645 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0202 |
2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.523-3231T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991645 | |||||||
chr17:18991668 | T | C | 32 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0038 others(29): Show |
38 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.523-3254A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991668 | |||||||
chr17:18991719 | G | A | 2 | a0001c0001t0003g0132 a0001c0001t0011g0065 |
2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.523-3305C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991719 | |||||||
chr17:18991796 | AGTGGTCC others(5): Show |
A | 1 | a0002c0002t0002g0134 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.523-3394_523-3383d others(14): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991796 | |||||||
chr17:18991898 | C | T | 1 | a0002c0002t0002g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.523-3484G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18991898 | |||||||
chr17:18992098 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.523-3684G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18992098 | |||||||
chr17:18992147 | C | T | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.523-3733G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18992147 | |||||||
chr17:18992502 | G | A | 1 | a0004c0004t0001g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.523-4088C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18992502 | |||||||
chr17:18992899 | A | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0038 others(25): Show |
35 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.523-4485T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18992899 | |||||||
chr17:18992984 | C | G | 27 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0038 others(24): Show |
33 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.523-4570G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18992984 | |||||||
chr17:18993067 | G | A | 65 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(62): Show |
90 | HG00280.hp1 HG00735.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.523-4653C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993067 | |||||||
chr17:18993088 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.523-4674C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993088 | |||||||
chr17:18993151 | C | A | 4 | a0001c0001t0007g0066 a0003c0003t0007g0153 a0003c0003t0007g0154 others(1): Show |
4 | HG02109.hp1 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-4737G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993151 | |||||||
chr17:18993200 | C | G | 1 | a0001c0001t0004g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.523-4786G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993200 | |||||||
chr17:18993517 | C | G | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.523-5103G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993517 | |||||||
chr17:18993704 | C | G | 71 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(68): Show |
94 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(91): Show |
intron_variant | MODIFIER | c.523-5290G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993704 | |||||||
chr17:18993817 | T | G | 3 | a0001c0001t0003g0252 a0002c0002t0002g0200 a0002c0002t0002g0201 |
3 | HG00639.hp1 HG01175.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.523-5403A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993817 | |||||||
chr17:18993986 | C | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0084 others(23): Show |
38 | HG01891.hp2 HG02004.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.523-5572G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18993986 | |||||||
chr17:18994025 | C | G | 74 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0021 others(71): Show |
98 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(95): Show |
intron_variant | MODIFIER | c.523-5611G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994025 | |||||||
chr17:18994150 | C | T | 1 | a0001c0001t0013g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.523-5736G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994150 | |||||||
chr17:18994359 | G | A | 85 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0079 others(82): Show |
104 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.523-5945C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994359 | |||||||
chr17:18994406 | G | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0112 others(17): Show |
25 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.523-5992C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994406 | |||||||
chr17:18994419 | G | A | 4 | a0003c0003t0001g0028 a0003c0003t0001g0158 a0003c0003t0001g0218 others(1): Show |
5 | HG02622.hp1 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-6005C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994419 | |||||||
chr17:18994493 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.523-6079C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994493 | |||||||
chr17:18994675 | T | A | 5 | a0001c0001t0004g0194 a0001c0001t0009g0192 a0002c0002t0002g0032 others(2): Show |
6 | HG02055.hp2 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.523-6261A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994675 | |||||||
chr17:18994687 | T | G | 180 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0022 others(177): Show |
224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.523-6273A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994687 | |||||||
chr17:18994688 | G | A | 38 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0068 others(35): Show |
47 | HG00741.hp1 HG01070.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.523-6274C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994688 | |||||||
chr17:18994739 | C | T | 1 | a0001c0001t0003g0083 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.523-6325G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994739 | |||||||
chr17:18994818 | A | T | 11 | a0001c0001t0003g0187 a0001c0001t0004g0190 a0001c0001t0004g0194 others(8): Show |
16 | HG01433.hp2 HG02055.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.523-6404T>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18994818 | |||||||
chr17:18995198 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0034 others(22): Show |
43 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.523-6784C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18995198 | |||||||
chr17:18995224 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0034 others(25): Show |
46 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.523-6810T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18995224 | |||||||
chr17:18995308 | G | A | 1 | a0003c0003t0001g0289 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.523-6894C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18995308 | |||||||
chr17:18995401 | T | C | 14 | a0001c0001t0003g0044 a0003c0003t0001g0255 a0003c0003t0001g0258 others(11): Show |
14 | HG02056.hp1 HG02132.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.523-6987A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18995401 | |||||||
chr17:18995864 | C | T | 1 | a0001c0001t0004g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.523-7450G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18995864 | |||||||
chr17:18995911 | T | TA | 56 | a0001c0001t0001g0079 a0001c0001t0001g0138 a0001c0001t0004g0133 others(53): Show |
68 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.523-7498dupT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18995911 | |||||||
chr17:18995911 | TA | T | 20 | a0001c0001t0001g0189 a0001c0001t0001g0229 a0002c0002t0002g0080 others(17): Show |
24 | HG00741.hp1 HG01070.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.523-7498delT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18995911 | |||||||
chr17:18996061 | A | G | 57 | a0001c0001t0001g0079 a0001c0001t0001g0138 a0001c0001t0004g0133 others(54): Show |
69 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.522+7459T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996061 | |||||||
chr17:18996096 | A | G | 73 | a0001c0001t0001g0079 a0001c0001t0001g0138 a0001c0001t0001g0189 others(70): Show |
90 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.522+7424T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996096 | |||||||
chr17:18996136 | G | GA | 50 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0034 others(47): Show |
72 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.522+7383dupT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996136 | |||||||
chr17:18996136 | G | GAA | 55 | a0001c0001t0001g0138 a0001c0001t0004g0133 a0002c0002t0002g0015 others(52): Show |
67 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.522+7382_522+7383d others(4): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996136 | |||||||
chr17:18996150 | T | A | 1 | a0003c0003t0001g0166 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.522+7370A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996150 | |||||||
chr17:18996151 | C | T | 1 | a0003c0003t0001g0166 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.522+7369G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996151 | |||||||
chr17:18996152 | A | C | 1 | a0003c0003t0001g0166 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.522+7368T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996152 | |||||||
chr17:18996221 | TA | T | 10 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
10 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.522+7298delT | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996221 | |||||||
chr17:18996297 | G | A | 14 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0001g0157 others(11): Show |
18 | HG00741.hp1 HG01070.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.522+7223C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996297 | |||||||
chr17:18996389 | A | C | 1 | a0001c0005t0001g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.522+7131T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996389 | |||||||
chr17:18996416 | G | C | 1 | a0003c0003t0001g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.522+7104C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996416 | |||||||
chr17:18996427 | T | C | 1 | a0002c0002t0002g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.522+7093A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996427 | |||||||
chr17:18996585 | A | G | 1 | a0002c0002t0002g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.522+6935T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996585 | |||||||
chr17:18996636 | A | G | 1 | a0002c0002t0002g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.522+6884T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996636 | |||||||
chr17:18996654 | G | A | 3 | a0001c0001t0003g0187 a0002c0002t0002g0008 a0002c0002t0002g0217 |
6 | HG02717.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+6866C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996654 | |||||||
chr17:18996761 | G | A | 25 | a0003c0003t0001g0007 a0003c0003t0001g0017 a0003c0003t0001g0030 others(22): Show |
31 | HG00609.hp1 HG00673.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.522+6759C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996761 | |||||||
chr17:18996946 | C | T | 1 | a0004c0004t0002g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.522+6574G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18996946 | |||||||
chr17:18997023 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.522+6497G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997023 | |||||||
chr17:18997226 | C | A | 2 | a0001c0001t0003g0132 a0001c0001t0011g0065 |
2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.522+6294G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997226 | |||||||
chr17:18997254 | G | C | 2 | a0001c0001t0001g0147 a0001c0005t0001g0148 |
2 | NA18973.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.522+6266C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997254 | |||||||
chr17:18997343 | G | C | 1 | a0001c0005t0001g0148 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.522+6177C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997343 | |||||||
chr17:18997433 | C | T | 28 | a0003c0003t0001g0007 a0003c0003t0001g0017 a0003c0003t0001g0030 others(25): Show |
34 | HG00609.hp1 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.522+6087G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997433 | |||||||
chr17:18997475 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0034 others(129): Show |
172 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.522+6045G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997475 | |||||||
chr17:18997553 | G | A | 50 | a0001c0001t0001g0138 a0001c0001t0004g0133 a0003c0003t0001g0042 others(47): Show |
59 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.522+5967C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997553 | |||||||
chr17:18997562 | A | G | 1 | a0001c0001t0007g0066 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.522+5958T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997562 | |||||||
chr17:18997573 | T | C | 3 | a0003c0003t0001g0291 a0003c0011t0010g0029 a0004c0004t0002g0161 |
4 | HG00741.hp1 HG01070.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+5947A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997573 | |||||||
chr17:18997854 | T | C | 52 | a0001c0001t0001g0138 a0001c0001t0003g0044 a0003c0003t0001g0042 others(49): Show |
61 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.522+5666A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997854 | |||||||
chr17:18997863 | CAG | C | 5 | a0001c0001t0001g0053 a0001c0001t0004g0054 a0001c0001t0004g0055 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+5655_522+5656d others(4): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997863 | |||||||
chr17:18997889 | T | C | 1 | a0002c0002t0002g0134 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.522+5631A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997889 | |||||||
chr17:18997890 | C | T | 1 | a0004c0004t0005g0294 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.522+5630G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997890 | |||||||
chr17:18997912 | T | C | 28 | a0003c0003t0001g0007 a0003c0003t0001g0017 a0003c0003t0001g0030 others(25): Show |
34 | HG00609.hp1 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.522+5608A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18997912 | |||||||
chr17:18998074 | C | G | 1 | a0004c0004t0002g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.522+5446G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998074 | |||||||
chr17:18998105 | G | A | 1 | a0002c0002t0002g0135 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.522+5415C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998105 | |||||||
chr17:18998168 | C | T | 1 | a0002c0012t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.522+5352G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998168 | |||||||
chr17:18998174 | G | C | 37 | a0001c0001t0001g0138 a0003c0003t0001g0042 a0003c0003t0001g0163 others(34): Show |
46 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.522+5346C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998174 | |||||||
chr17:18998175 | G | A | 37 | a0001c0001t0001g0138 a0003c0003t0001g0042 a0003c0003t0001g0163 others(34): Show |
46 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.522+5345C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998175 | |||||||
chr17:18998366 | C | A | 15 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0001g0157 others(12): Show |
19 | HG00741.hp1 HG01070.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.522+5154G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998366 | |||||||
chr17:18998488 | C | T | 1 | a0014c0021t0028g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.522+5032G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998488 | |||||||
chr17:18998565 | G | A | 1 | a0005c0008t0002g0253 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.522+4955C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998565 | |||||||
chr17:18998651 | G | C | 1 | a0003c0003t0003g0266 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.522+4869C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998651 | |||||||
chr17:18998790 | C | T | 1 | a0004c0004t0002g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.522+4730G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18998790 | |||||||
chr17:18999001 | C | T | 1 | a0004c0006t0001g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.522+4519G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999001 | |||||||
chr17:18999007 | C | T | 15 | a0001c0001t0001g0189 a0001c0001t0001g0196 a0001c0001t0003g0187 others(12): Show |
20 | HG00408.hp2 HG01433.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.522+4513G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999007 | |||||||
chr17:18999151 | A | G | 97 | a0001c0001t0001g0138 a0001c0001t0003g0044 a0003c0003t0001g0007 others(94): Show |
117 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.522+4369T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999151 | |||||||
chr17:18999250 | C | A | 1 | a0002c0002t0002g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.522+4270G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999250 | |||||||
chr17:18999256 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.522+4264G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999256 | |||||||
chr17:18999314 | C | T | 1 | a0004c0004t0002g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.522+4206G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999314 | |||||||
chr17:18999411 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.522+4109C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999411 | |||||||
chr17:18999439 | C | T | 15 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0001g0157 others(12): Show |
19 | HG00741.hp1 HG01070.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.522+4081G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999439 | |||||||
chr17:18999475 | A | G | 1 | a0001c0001t0011g0065 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.522+4045T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999475 | |||||||
chr17:18999479 | C | A | 81 | a0001c0001t0001g0138 a0003c0003t0001g0007 a0003c0003t0001g0017 others(78): Show |
101 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.522+4041G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999479 | |||||||
chr17:18999480 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.522+4040T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999480 | |||||||
chr17:18999607 | G | A | 1 | a0009c0013t0003g0292 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.522+3913C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999607 | |||||||
chr17:18999609 | G | A | 1 | a0003c0016t0003g0293 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.522+3911C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999609 | |||||||
chr17:18999803 | T | C | 1 | a0004c0004t0005g0294 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.522+3717A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 18999803 | |||||||
chr17:19000086 | G | A | 1 | a0002c0002t0002g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.522+3434C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19000086 | |||||||
chr17:19000101 | C | T | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.522+3419G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19000101 | |||||||
chr17:19000194 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0064 |
4 | NA18948.hp1 NA18985.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+3326G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19000194 | |||||||
chr17:19000263 | T | C | 95 | a0001c0001t0001g0138 a0003c0003t0001g0007 a0003c0003t0001g0017 others(92): Show |
115 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.522+3257A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19000263 | |||||||
chr17:19000686 | C | T | 2 | a0001c0001t0009g0227 a0002c0002t0002g0035 |
3 | HG02280.hp2 HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.522+2834G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19000686 | |||||||
chr17:19000711 | T | A | 1 | a0003c0003t0012g0043 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.522+2809A>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19000711 | |||||||
chr17:19000789 | C | T | 1 | a0014c0021t0028g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.522+2731G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19000789 | |||||||
chr17:19001042 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.522+2478T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001042 | |||||||
chr17:19001065 | A | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.522+2455T>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001065 | |||||||
chr17:19001118 | T | C | 50 | a0003c0003t0001g0042 a0003c0003t0001g0163 a0003c0003t0001g0255 others(47): Show |
59 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.522+2402A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001118 | |||||||
chr17:19001225 | G | A | 2 | a0001c0001t0003g0252 a0002c0002t0002g0251 |
2 | HG00639.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.522+2295C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001225 | |||||||
chr17:19001356 | C | T | 1 | a0013c0025t0001g0057 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.522+2164G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001356 | |||||||
chr17:19001491 | T | C | 15 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0001g0157 others(12): Show |
19 | HG00741.hp1 HG01070.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.522+2029A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001491 | |||||||
chr17:19001517 | A | G | 93 | a0003c0003t0001g0007 a0003c0003t0001g0017 a0003c0003t0001g0026 others(90): Show |
113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.522+2003T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001517 | |||||||
chr17:19001526 | G | A | 12 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
17 | HG00408.hp1 HG02165.hp2 NA18960.hp2 others(14): Show |
intron_variant | MODIFIER | c.522+1994C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001526 | |||||||
chr17:19001690 | G | A | 1 | a0002c0012t0006g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.522+1830C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001690 | |||||||
chr17:19001794 | G | A | 2 | a0003c0003t0001g0007 a0003c0007t0003g0186 |
5 | NA18942.hp1 NA18965.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+1726C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001794 | |||||||
chr17:19001800 | C | CG | 6 | a0001c0001t0001g0222 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | HG01099.hp1 HG01243.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+1719dupC | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001800 | |||||||
chr17:19001863 | A | G | 15 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0001g0157 others(12): Show |
19 | HG00741.hp1 HG01070.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.522+1657T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19001863 | |||||||
chr17:19002062 | A | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0034 others(131): Show |
174 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.522+1458T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19002062 | |||||||
chr17:19002118 | C | CCCT | 40 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0034 others(37): Show |
60 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.522+1399_522+1401d others(5): Show |
FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19002118 | |||||||
chr17:19002317 | G | A | 27 | a0003c0003t0001g0007 a0003c0003t0001g0017 a0003c0003t0001g0030 others(24): Show |
33 | HG00609.hp1 HG00673.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.522+1203C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19002317 | |||||||
chr17:19002485 | T | C | 27 | a0003c0003t0001g0007 a0003c0003t0001g0017 a0003c0003t0001g0030 others(24): Show |
33 | HG00609.hp1 HG00673.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.522+1035A>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19002485 | |||||||
chr17:19002716 | C | T | 1 | a0005c0008t0002g0253 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.522+804G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19002716 | |||||||
chr17:19002728 | G | T | 13 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0053 others(10): Show |
13 | HG00140.hp2 HG01256.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.522+792C>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19002728 | |||||||
chr17:19002729 | C | T | 13 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0053 others(10): Show |
13 | HG00140.hp2 HG01256.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.522+791G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19002729 | |||||||
chr17:19003291 | G | A | 1 | a0002c0012t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.522+229C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19003291 | |||||||
chr17:19003411 | C | G | 1 | a0002c0002t0002g0220 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.522+109G>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19003411 | |||||||
chr17:19003456 | C | T | 2 | a0003c0003t0007g0153 a0003c0003t0007g0154 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.522+64G>A | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 2/5 | chr17 | 19003456 | |||||||
chr17:19004194 | G | A | 1 | a0003c0003t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-128-25C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/5 | chr17 | 19004194 | |||||||
chr17:19004206 | A | G | 1 | a0003c0003t0001g0152 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-128-37T>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/5 | chr17 | 19004206 | |||||||
chr17:19004210 | C | A | 2 | a0001c0001t0008g0016 a0001c0005t0001g0151 |
4 | NA18952.hp1 NA18983.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128-41G>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/5 | chr17 | 19004210 | |||||||
chr17:19004284 | G | A | 1 | a0003c0003t0007g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-128-115C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/5 | chr17 | 19004284 | |||||||
chr17:19004360 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0034 others(131): Show |
174 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-128-191C>G | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/5 | chr17 | 19004360 | |||||||
chr17:19004460 | T | G | 38 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(35): Show |
49 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-129+249A>C | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/5 | chr17 | 19004460 | |||||||
chr17:19004621 | G | A | 48 | a0003c0003t0001g0042 a0003c0003t0001g0255 a0003c0003t0001g0258 others(45): Show |
57 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-129+88C>T | FAM83G | ENSG00000188522.16 | transcript | ENST00000388995.11 | protein_coding | 1/5 | chr17 | 19004621 |