Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 345757 |
| ensemblid | ENSG00000174132.9 |
| hgncid | 24943 |
| symbol | FAM174A |
| name | family with sequence similarity 174 member A |
| refseq_nuc | NM_198507.3 |
| refseq_prot | NP_940909.1 |
| ensembl_nuc | ENST00000312637.5 |
| ensembl_prot | ENSP00000307954.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 100535374 |
| end | 100586741 |
| strand | + |
| ver | v1.2 |
| region | chr5:100535374-100586741 |
| region5000 | chr5:100530374-100591741 |
| regionname0 | FAM174A_chr5_100535374_100586741 |
| regionname5000 | FAM174A_chr5_100530374_100591741 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 189 | 285 | 78 | 61 | 111 | 14 | 19 | 81 | FAM174A_chr5_100530374_100591741 | FAM174A | MKASQ others(184): Show |
chr5 | 100530374 | 100591741 |
| a0002 | 0/0 | 189 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | MKASQ others(184): Show |
chr5 | 100530374 | 100591741 |
| a0003 | 0/0 | 189 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | MKASQ others(184): Show |
chr5 | 100530374 | 100591741 |
| a0004 | 0/0 | 189 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | MKASQ others(184): Show |
chr5 | 100530374 | 100591741 |
| a0005 | 0/0 | 189 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | MKASQ others(184): Show |
chr5 | 100530374 | 100591741 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 569 | 230 | 59 | 39 | 102 | 11 | 17 | FAM174A_chr5_100530374_100591741 | FAM174A | ATGAA others(564): Show |
chr5 | 100530374 | 100591741 | ||
| a0001c0002 | 0/0 | 569 | 54 | 19 | 22 | 8 | 3 | 2 | FAM174A_chr5_100530374_100591741 | FAM174A | ATGAA others(564): Show |
chr5 | 100530374 | 100591741 | ||
| a0001c0005 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | ATGAA others(564): Show |
chr5 | 100530374 | 100591741 | ||
| a0002c0003 | 0/0 | 569 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | ATGAA others(564): Show |
chr5 | 100530374 | 100591741 | ||
| a0003c0004 | 0/0 | 569 | 3 | 3 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | ATGAA others(564): Show |
chr5 | 100530374 | 100591741 | ||
| a0004c0007 | 0/0 | 569 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | ATGAA others(564): Show |
chr5 | 100530374 | 100591741 | ||
| a0005c0006 | 0/0 | 569 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | ATGAA others(564): Show |
chr5 | 100530374 | 100591741 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1286 | 77 | 40 | 8 | 19 | 4 | 6 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0001t0002 | 1/1 | 1286 | 131 | 4 | 27 | 81 | 7 | 10 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0001t0003 | 0/0 | 1286 | 16 | 12 | 3 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0001t0004 | 0/0 | 1286 | 3 | 2 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0001t0005 | 0/0 | 1286 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0001t0007 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0002t0001 | 0/0 | 1286 | 53 | 19 | 22 | 8 | 3 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0002t0006 | 0/0 | 1286 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0001c0005t0008 | 0/0 | 1286 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0002c0003t0001 | 0/0 | 1286 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0003c0004t0003 | 0/0 | 1286 | 3 | 3 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0004c0007t0001 | 0/0 | 1286 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| a0005c0006t0002 | 0/0 | 1286 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | AGCTG others(1281): Show |
chr5 | 100530374 | 100591741 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0023 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0004g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0001c0005t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0002c0003t0001g0001 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0002c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0003c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0003c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0003c0004t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0004c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| a0005c0006t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0238 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0182 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00738 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0229 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0065 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0233 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0064 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02735 | hp2 | a0001 | c0002 | t0006 | g0237 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02965 | hp2 | a0003 | c0004 | t0003 | g0248 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03834 | hp1 | a0004 | c0007 | t0001 | g0003 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18964 | hp1 | a0005 | c0006 | t0002 | g0018 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18977 | hp1 | a0001 | c0005 | t0008 | g0250 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19030 | hp1 | a0003 | c0004 | t0003 | g0041 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ASW | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0183 | EUR | TSI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0230 | EUR | TSI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA20300 | hp1 | a0003 | c0004 | t0003 | g0036 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0023 | REF | REF | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0172 | REF | REF | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:100535612 | G | C | 1 | a0005 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.82G>C | p.Gly28Arg | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 239/1287 | 82/573 | 28/190 | chr5 | 100535612 | |||
| chr5:100535655 | G | A | 1 | a0004 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.125G>A | p.Gly42Asp | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 282/1287 | 125/573 | 42/190 | chr5 | 100535655 | |||
| chr5:100535814 | A | G | 1 | a0002 | 8 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
missense_variant | MODERATE | c.284A>G | p.Asp95Gly | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 441/1287 | 284/573 | 95/190 | chr5 | 100535814 | |||
| chr5:100562176 | A | G | 1 | a0003 | 3 | HG02965.hp2 NA19030.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.557A>G | p.Asn186Ser | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/3 | 714/1287 | 557/573 | 186/190 | chr5 | 100562176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:100535602 | T | C | 1 | a0001c0005 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.72T>C | p.Pro24Pro | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 229/1287 | 72/573 | 24/190 | chr5 | 100535602 | |||
| chr5:100562162 | G | A | 1 | a0001c0002 | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
synonymous_variant | LOW | c.543G>A | p.Thr181Thr | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/3 | 700/1287 | 543/573 | 181/190 | chr5 | 100562162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:100535393 | T | A | 1 | a0001c0001t0004 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-138T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 138 | chr5 | 100535393 | ||||||
| chr5:100535437 | C | G | 1 | a0001c0005t0008 | 1 | NA18977.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 94 | chr5 | 100535437 | ||||||
| chr5:100586373 | C | T | 1 | a0001c0001t0007 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 189 | chr5 | 100586373 | ||||||
| chr5:100586377 | G | A | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(6): Show |
163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*193G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 193 | chr5 | 100586377 | ||||||
| chr5:100586448 | C | T | 1 | a0001c0001t0005 | 2 | HG00597.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*264C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 264 | chr5 | 100586448 | ||||||
| chr5:100586460 | A | G | 2 | a0001c0001t0003 a0003c0004t0003 |
19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*276A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 276 | chr5 | 100586460 | ||||||
| chr5:100586649 | A | T | 1 | a0001c0002t0006 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 465 | chr5 | 100586649 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:100535992 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.434+28C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100535992 | |||||||
| chr5:100536008 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.434+44C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536008 | |||||||
| chr5:100536082 | T | G | 1 | a0001c0001t0002g0032 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.434+118T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536082 | |||||||
| chr5:100536346 | A | G | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.434+382A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536346 | |||||||
| chr5:100536374 | A | G | 3 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0253 |
3 | NA19057.hp1 NA19063.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.434+410A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536374 | |||||||
| chr5:100536563 | C | T | 1 | a0001c0005t0008g0250 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.434+599C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536563 | |||||||
| chr5:100536650 | T | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434+686T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536650 | |||||||
| chr5:100536748 | G | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+784G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536748 | |||||||
| chr5:100536765 | C | T | 1 | a0003c0004t0003g0248 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434+801C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536765 | |||||||
| chr5:100536820 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.434+856T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536820 | |||||||
| chr5:100536890 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434+926A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536890 | |||||||
| chr5:100537355 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.434+1391C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537355 | |||||||
| chr5:100537416 | G | C | 13 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(10): Show |
15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.434+1452G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537416 | |||||||
| chr5:100537545 | A | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+1581A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537545 | |||||||
| chr5:100537662 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.434+1698G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537662 | |||||||
| chr5:100537750 | A | G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.434+1786A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537750 | |||||||
| chr5:100537817 | A | G | 36 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(33): Show |
45 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.434+1853A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537817 | |||||||
| chr5:100537837 | A | G | 46 | a0001c0001t0002g0216 a0001c0002t0001g0002 a0001c0002t0001g0026 others(43): Show |
55 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.434+1873A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537837 | |||||||
| chr5:100537933 | A | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+1969A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537933 | |||||||
| chr5:100538045 | T | C | 1 | a0001c0001t0002g0047 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.434+2081T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538045 | |||||||
| chr5:100538235 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.434+2271C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538235 | |||||||
| chr5:100538337 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0207 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+2373G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538337 | |||||||
| chr5:100538380 | A | C | 1 | a0001c0001t0003g0206 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.434+2416A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538380 | |||||||
| chr5:100538529 | G | GTA | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0002t0001g0246 |
3 | HG00741.hp2 HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434+2577_434+2578d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100538529 | ||||||
| chr5:100538554 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+2590G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538554 | |||||||
| chr5:100538599 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.434+2635G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538599 | |||||||
| chr5:100538657 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434+2693A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538657 | |||||||
| chr5:100538717 | A | G | 2 | a0001c0002t0001g0214 a0001c0002t0001g0215 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.434+2753A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538717 | |||||||
| chr5:100538849 | T | G | 27 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(24): Show |
35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.434+2885T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538849 | |||||||
| chr5:100539018 | G | A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.434+3054G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539018 | |||||||
| chr5:100539028 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.434+3064C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539028 | |||||||
| chr5:100539053 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+3089G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539053 | |||||||
| chr5:100539075 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.434+3111T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539075 | |||||||
| chr5:100539084 | T | TTAAAAAA others(318): Show |
1 | a0003c0004t0003g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.434+3120_434+3121i others(327): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539084 | |||||||
| chr5:100539085 | A | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(119): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.434+3121A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539085 | |||||||
| chr5:100539086 | A | T | 31 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(28): Show |
39 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.434+3122A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539086 | |||||||
| chr5:100539287 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.434+3323A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539287 | |||||||
| chr5:100539370 | T | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0207 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+3406T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539370 | |||||||
| chr5:100539385 | T | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.434+3421T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539385 | |||||||
| chr5:100539566 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+3602G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539566 | |||||||
| chr5:100539835 | T | C | 5 | a0001c0002t0001g0239 a0001c0002t0001g0240 a0001c0002t0001g0241 others(2): Show |
5 | HG02647.hp2 HG02717.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.434+3871T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539835 | |||||||
| chr5:100539907 | A | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+3943A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539907 | |||||||
| chr5:100539948 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+3984G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539948 | |||||||
| chr5:100539966 | A | T | 1 | a0001c0001t0002g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.434+4002A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539966 | |||||||
| chr5:100540229 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.434+4265A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540229 | |||||||
| chr5:100540338 | T | A | 2 | a0001c0001t0003g0056 a0001c0001t0003g0206 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.434+4374T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540338 | |||||||
| chr5:100540347 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434+4383T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540347 | |||||||
| chr5:100540448 | A | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+4484A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540448 | |||||||
| chr5:100540498 | T | G | 11 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0038 others(8): Show |
13 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.434+4534T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540498 | |||||||
| chr5:100540499 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434+4535A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540499 | |||||||
| chr5:100540553 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.434+4589A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540553 | |||||||
| chr5:100540658 | C | CT | 10 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 others(7): Show |
13 | HG00140.hp2 HG01167.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.434+4695dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100540658 | ||||||
| chr5:100540899 | G | A | 5 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0233 others(2): Show |
7 | HG01167.hp2 HG01934.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+4935G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540899 | |||||||
| chr5:100541011 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.434+5047A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541011 | |||||||
| chr5:100541052 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0098 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.434+5088G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541052 | |||||||
| chr5:100541160 | A | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.434+5196A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541160 | |||||||
| chr5:100541321 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.434+5357G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541321 | |||||||
| chr5:100541630 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.434+5666A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541630 | |||||||
| chr5:100541880 | T | A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+5916T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541880 | |||||||
| chr5:100542299 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+6335G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542299 | |||||||
| chr5:100542328 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(169): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.434+6364T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542328 | |||||||
| chr5:100542511 | C | T | 1 | a0001c0002t0001g0232 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.434+6547C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542511 | |||||||
| chr5:100542531 | A | G | 1 | a0001c0001t0002g0025 | 2 | HG01934.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.434+6567A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542531 | |||||||
| chr5:100542583 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.434+6619A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542583 | |||||||
| chr5:100542621 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.434+6657A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542621 | |||||||
| chr5:100542659 | A | AC | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.434+6696dupC | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542659 | ||||||
| chr5:100542731 | C | T | 10 | a0001c0001t0002g0046 a0001c0001t0002g0192 a0001c0001t0002g0193 others(7): Show |
11 | HG00597.hp2 HG01928.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.434+6767C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542731 | |||||||
| chr5:100542758 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+6794C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542758 | |||||||
| chr5:100542846 | A | ATATG | 7 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
8 | HG01109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+6883_434+6884i others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | ||||||
| chr5:100542846 | A | ATGTG | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+6898_434+6901d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | ||||||
| chr5:100542846 | A | G | 27 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(24): Show |
35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.434+6882A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542846 | |||||||
| chr5:100542846 | ATG | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0052 others(5): Show |
13 | HG00738.hp1 HG00741.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.434+6900_434+6901d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | ||||||
| chr5:100542846 | ATGTGTG | A | 4 | a0001c0001t0003g0056 a0001c0001t0003g0062 a0001c0001t0003g0063 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+6896_434+6901d others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | ||||||
| chr5:100542850 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0052 |
3 | HG00741.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434+6886G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542850 | |||||||
| chr5:100542934 | T | C | 1 | a0001c0001t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.434+6970T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542934 | |||||||
| chr5:100543043 | A | T | 1 | a0001c0002t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.434+7079A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543043 | |||||||
| chr5:100543075 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.434+7111C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543075 | |||||||
| chr5:100543079 | G | A | 6 | a0001c0001t0002g0017 a0001c0001t0002g0100 a0001c0001t0002g0101 others(3): Show |
7 | NA18945.hp1 NA18948.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+7115G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543079 | |||||||
| chr5:100543211 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434+7247G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543211 | |||||||
| chr5:100543262 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7298C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543262 | |||||||
| chr5:100543263 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
60 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.434+7299G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543263 | |||||||
| chr5:100543301 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.434+7337A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543301 | |||||||
| chr5:100543436 | G | A | 1 | a0001c0002t0001g0217 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.434+7472G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543436 | |||||||
| chr5:100543550 | C | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7586C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543550 | |||||||
| chr5:100543676 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.434+7712A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543676 | |||||||
| chr5:100543790 | C | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7826C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543790 | |||||||
| chr5:100543820 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7856G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543820 | |||||||
| chr5:100543952 | G | T | 1 | a0001c0001t0002g0190 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.434+7988G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543952 | |||||||
| chr5:100543991 | A | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0050 others(8): Show |
12 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.434+8027A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543991 | |||||||
| chr5:100544036 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.434+8072G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544036 | |||||||
| chr5:100544345 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0207 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+8381G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544345 | |||||||
| chr5:100544348 | ATACCCCT others(7): Show |
A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.434+8402_434+8415d others(16): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100544348 | ||||||
| chr5:100544427 | G | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+8463G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544427 | |||||||
| chr5:100544472 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+8508G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544472 | |||||||
| chr5:100544949 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+8985C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544949 | |||||||
| chr5:100544964 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0207 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+9000T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544964 | |||||||
| chr5:100545067 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+9103A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545067 | |||||||
| chr5:100545375 | T | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+9411T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545375 | |||||||
| chr5:100545378 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+9414G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545378 | |||||||
| chr5:100545511 | C | A | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.434+9547C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545511 | |||||||
| chr5:100545557 | G | T | 3 | a0002c0003t0001g0001 a0002c0003t0001g0064 a0002c0003t0001g0065 |
8 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+9593G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545557 | |||||||
| chr5:100545682 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.434+9718A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545682 | |||||||
| chr5:100545729 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.434+9765T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545729 | |||||||
| chr5:100545904 | T | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+9940T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545904 | |||||||
| chr5:100545976 | C | A | 1 | a0001c0001t0002g0019 | 2 | NA18941.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.434+10012C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545976 | |||||||
| chr5:100546009 | T | C | 1 | a0001c0001t0002g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.434+10045T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546009 | |||||||
| chr5:100546034 | G | A | 4 | a0001c0001t0002g0046 a0001c0001t0002g0192 a0001c0001t0002g0193 others(1): Show |
4 | HG04228.hp1 NA18612.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+10070G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546034 | |||||||
| chr5:100546071 | A | G | 1 | a0001c0002t0001g0231 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.434+10107A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546071 | |||||||
| chr5:100546437 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+10473G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546437 | |||||||
| chr5:100546715 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
96 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.434+10751C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546715 | |||||||
| chr5:100546730 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+10766A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546730 | |||||||
| chr5:100546792 | C | T | 13 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(10): Show |
15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.434+10828C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546792 | |||||||
| chr5:100547603 | T | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.434+11639T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547603 | |||||||
| chr5:100547648 | C | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0226 a0001c0002t0001g0227 others(4): Show |
11 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.434+11684C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547648 | |||||||
| chr5:100547667 | G | A | 34 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(31): Show |
42 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.434+11703G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547667 | |||||||
| chr5:100547677 | T | C | 8 | a0001c0001t0003g0006 a0001c0001t0003g0038 a0001c0001t0003g0039 others(5): Show |
9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.434+11713T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547677 | |||||||
| chr5:100547752 | G | T | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG00408.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.434+11788G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547752 | |||||||
| chr5:100547833 | TA | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+11870delA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547833 | |||||||
| chr5:100547834 | A | AT | 5 | a0001c0001t0002g0046 a0001c0001t0004g0030 a0001c0001t0004g0249 others(2): Show |
6 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+11880dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100547834 | ||||||
| chr5:100547834 | A | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+11870A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547834 | |||||||
| chr5:100547873 | G | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
55 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.434+11909G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547873 | |||||||
| chr5:100547928 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.434+11964C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547928 | |||||||
| chr5:100548025 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+12061A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548025 | |||||||
| chr5:100548054 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+12090T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548054 | |||||||
| chr5:100548604 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+12640G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548604 | |||||||
| chr5:100548612 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.434+12648G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548612 | |||||||
| chr5:100548921 | TCA | T | 6 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+12959_434+1296 others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100548921 | ||||||
| chr5:100549167 | G | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-12887G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549167 | |||||||
| chr5:100549188 | G | C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-12866G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549188 | |||||||
| chr5:100549261 | A | G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.435-12793A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549261 | |||||||
| chr5:100549478 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.435-12576T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549478 | |||||||
| chr5:100549607 | AT | A | 6 | a0001c0002t0001g0217 a0001c0002t0001g0239 a0001c0002t0001g0240 others(3): Show |
6 | HG02647.hp2 HG02717.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-12431delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100549607 | ||||||
| chr5:100549821 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-12233C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549821 | |||||||
| chr5:100549932 | T | G | 1 | a0001c0002t0001g0236 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.435-12122T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549932 | |||||||
| chr5:100550043 | A | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-12011A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550043 | |||||||
| chr5:100550067 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.435-11987G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550067 | |||||||
| chr5:100550384 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0085 a0001c0001t0001g0086 |
4 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-11670C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550384 | |||||||
| chr5:100550710 | G | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-11344G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550710 | |||||||
| chr5:100550842 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.435-11212A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550842 | |||||||
| chr5:100551315 | A | G | 1 | a0001c0001t0005g0024 | 2 | HG00597.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.435-10739A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551315 | |||||||
| chr5:100551377 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.435-10677C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551377 | |||||||
| chr5:100551399 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.435-10655C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551399 | |||||||
| chr5:100551817 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.435-10237G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551817 | |||||||
| chr5:100551897 | A | G | 1 | a0001c0001t0001g0013 | 2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.435-10157A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551897 | |||||||
| chr5:100552128 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.435-9926G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552128 | |||||||
| chr5:100552309 | T | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-9745T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552309 | |||||||
| chr5:100552451 | A | T | 1 | a0001c0001t0002g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.435-9603A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552451 | |||||||
| chr5:100552491 | G | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-9563G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552491 | |||||||
| chr5:100552982 | A | G | 1 | a0001c0002t0001g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.435-9072A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552982 | |||||||
| chr5:100553034 | T | G | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-9020T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553034 | |||||||
| chr5:100553055 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.435-8999T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553055 | |||||||
| chr5:100553138 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.435-8916A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553138 | |||||||
| chr5:100553143 | C | G | 1 | a0001c0001t0002g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.435-8911C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553143 | |||||||
| chr5:100553223 | A | T | 27 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(24): Show |
35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.435-8831A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553223 | |||||||
| chr5:100553374 | T | C | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-8680T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553374 | |||||||
| chr5:100553397 | A | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-8657A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553397 | |||||||
| chr5:100553722 | A | G | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-8332A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553722 | |||||||
| chr5:100553954 | G | C | 1 | a0001c0001t0002g0135 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.435-8100G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553954 | |||||||
| chr5:100554009 | C | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.435-8045C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554009 | |||||||
| chr5:100554276 | C | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7778C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554276 | |||||||
| chr5:100554304 | TTCTA | T | 5 | a0001c0002t0001g0209 a0001c0002t0001g0210 a0001c0002t0001g0211 others(2): Show |
5 | HG01243.hp1 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-7746_435-7743d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554304 | ||||||
| chr5:100554310 | C | CT | 9 | a0001c0001t0002g0133 a0001c0001t0002g0183 a0001c0001t0003g0040 others(6): Show |
10 | HG01109.hp2 HG02451.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.435-7721dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554310 | ||||||
| chr5:100554310 | CT | C | 88 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0050 others(85): Show |
101 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.435-7721delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554310 | ||||||
| chr5:100554310 | CTT | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
67 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.435-7722_435-7721d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554310 | ||||||
| chr5:100554363 | C | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7691C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554363 | |||||||
| chr5:100554387 | G | A | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-7667G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554387 | |||||||
| chr5:100554447 | G | A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-7607G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554447 | |||||||
| chr5:100554462 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-7592G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554462 | |||||||
| chr5:100554604 | C | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7450C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554604 | |||||||
| chr5:100554643 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.435-7411A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554643 | |||||||
| chr5:100554643 | AT | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
96 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.435-7408delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554643 | ||||||
| chr5:100554868 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0138 a0001c0001t0002g0190 |
4 | HG00140.hp1 HG01071.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-7186G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554868 | |||||||
| chr5:100554882 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.435-7172A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554882 | |||||||
| chr5:100554904 | T | A | 4 | a0001c0001t0002g0018 a0001c0001t0002g0108 a0001c0001t0002g0109 others(1): Show |
4 | NA18964.hp1 NA18970.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-7150T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554904 | |||||||
| chr5:100554910 | T | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7144T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554910 | |||||||
| chr5:100554923 | G | A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-7131G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554923 | |||||||
| chr5:100554947 | C | T | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-7107C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554947 | |||||||
| chr5:100554957 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.435-7097T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554957 | |||||||
| chr5:100555041 | T | C | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-7013T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555041 | |||||||
| chr5:100555069 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0090 others(5): Show |
9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.435-6985C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555069 | |||||||
| chr5:100555077 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.435-6977C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555077 | |||||||
| chr5:100555092 | C | A | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.435-6962C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555092 | |||||||
| chr5:100555103 | G | A | 1 | a0001c0001t0002g0252 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.435-6951G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555103 | |||||||
| chr5:100555156 | G | C | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-6898G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555156 | |||||||
| chr5:100555197 | C | T | 17 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(14): Show |
19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.435-6857C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555197 | |||||||
| chr5:100555209 | G | C | 47 | a0001c0001t0004g0030 a0001c0001t0004g0249 a0001c0002t0001g0002 others(44): Show |
57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-6845G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555209 | |||||||
| chr5:100555244 | C | G | 1 | a0001c0001t0002g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.435-6810C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555244 | |||||||
| chr5:100555274 | G | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.435-6780G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555274 | |||||||
| chr5:100555433 | G | C | 27 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(24): Show |
35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.435-6621G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555433 | |||||||
| chr5:100555449 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.435-6605C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555449 | |||||||
| chr5:100555498 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.435-6556C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555498 | |||||||
| chr5:100555499 | G | A | 2 | a0001c0001t0002g0138 a0001c0002t0001g0218 |
2 | HG03942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.435-6555G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555499 | |||||||
| chr5:100555526 | C | G | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-6528C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555526 | |||||||
| chr5:100555538 | C | G | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-6516C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555538 | |||||||
| chr5:100555582 | T | C | 50 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 others(47): Show |
61 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.435-6472T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555582 | |||||||
| chr5:100555614 | C | T | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-6440C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555614 | |||||||
| chr5:100555656 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.435-6398G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555656 | |||||||
| chr5:100555707 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.435-6347G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555707 | |||||||
| chr5:100555778 | G | GT | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-6269dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100555778 | ||||||
| chr5:100555800 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.435-6254T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555800 | |||||||
| chr5:100555809 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-6245T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555809 | |||||||
| chr5:100555821 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-6233C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555821 | |||||||
| chr5:100555888 | A | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-6166A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555888 | |||||||
| chr5:100555897 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.435-6157G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555897 | |||||||
| chr5:100555930 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.435-6124G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555930 | |||||||
| chr5:100555941 | GT | G | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-6110delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100555941 | ||||||
| chr5:100556000 | G | A | 4 | a0001c0001t0003g0056 a0001c0001t0003g0062 a0001c0001t0003g0063 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-6054G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556000 | |||||||
| chr5:100556022 | C | T | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-6032C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556022 | |||||||
| chr5:100556065 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.435-5989T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556065 | |||||||
| chr5:100556151 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.435-5903C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556151 | |||||||
| chr5:100556161 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.435-5893G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556161 | |||||||
| chr5:100556303 | C | G | 2 | a0001c0001t0001g0128 a0001c0001t0002g0127 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.435-5751C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556303 | |||||||
| chr5:100556391 | C | T | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-5663C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556391 | |||||||
| chr5:100556493 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-5561C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556493 | |||||||
| chr5:100556543 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
99 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.435-5511T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556543 | |||||||
| chr5:100556549 | C | T | 37 | a0001c0001t0001g0128 a0001c0001t0002g0017 a0001c0001t0002g0018 others(34): Show |
38 | HG00621.hp2 HG01099.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.435-5505C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556549 | |||||||
| chr5:100556650 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.435-5404T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556650 | |||||||
| chr5:100556672 | A | G | 2 | a0001c0001t0003g0056 a0001c0001t0003g0206 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.435-5382A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556672 | |||||||
| chr5:100556702 | C | G | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-5352C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556702 | |||||||
| chr5:100556724 | C | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-5330C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556724 | |||||||
| chr5:100556740 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0042 a0001c0001t0003g0044 |
4 | HG01167.hp1 HG01169.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-5314G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556740 | |||||||
| chr5:100556956 | C | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-5098C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556956 | |||||||
| chr5:100557121 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.435-4933G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557121 | |||||||
| chr5:100557201 | C | A | 13 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(10): Show |
15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.435-4853C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557201 | |||||||
| chr5:100557220 | G | A | 6 | a0001c0001t0002g0136 a0001c0001t0002g0141 a0001c0001t0002g0142 others(3): Show |
6 | HG02056.hp1 HG02074.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.435-4834G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557220 | |||||||
| chr5:100557220 | G | GTTCTGTT | 50 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 others(47): Show |
61 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.435-4833_435-4832i others(9): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100557220 | ||||||
| chr5:100557223 | C | T | 50 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 others(47): Show |
61 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.435-4831C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557223 | |||||||
| chr5:100557273 | G | A | 46 | a0001c0001t0001g0069 a0001c0002t0001g0002 a0001c0002t0001g0026 others(43): Show |
55 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.435-4781G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557273 | |||||||
| chr5:100557288 | A | G | 1 | a0001c0001t0002g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.435-4766A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557288 | |||||||
| chr5:100557513 | A | G | 3 | a0001c0001t0004g0030 a0001c0001t0004g0249 a0001c0002t0001g0224 |
4 | HG01109.hp2 HG02451.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-4541A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557513 | |||||||
| chr5:100557544 | C | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.435-4510C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557544 | |||||||
| chr5:100557588 | G | T | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-4466G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557588 | |||||||
| chr5:100557593 | T | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0050 others(8): Show |
12 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.435-4461T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557593 | |||||||
| chr5:100557605 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
63 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.435-4449C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557605 | |||||||
| chr5:100557627 | T | G | 3 | a0002c0003t0001g0001 a0002c0003t0001g0064 a0002c0003t0001g0065 |
8 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.435-4427T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557627 | |||||||
| chr5:100557677 | T | C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-4377T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557677 | |||||||
| chr5:100557851 | G | A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-4203G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557851 | |||||||
| chr5:100557927 | C | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-4127C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557927 | |||||||
| chr5:100558032 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-4022C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558032 | |||||||
| chr5:100558033 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.435-4021G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558033 | |||||||
| chr5:100558046 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.435-4008A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558046 | |||||||
| chr5:100558203 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.435-3851G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558203 | |||||||
| chr5:100558233 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-3821T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558233 | |||||||
| chr5:100558293 | G | T | 1 | a0001c0001t0002g0126 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.435-3761G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558293 | |||||||
| chr5:100558343 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.435-3711G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558343 | |||||||
| chr5:100558428 | G | T | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-3626G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558428 | |||||||
| chr5:100558478 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.435-3576G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558478 | |||||||
| chr5:100558563 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0207 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.435-3491G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558563 | |||||||
| chr5:100558763 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.435-3291C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558763 | |||||||
| chr5:100558795 | T | C | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-3259T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558795 | |||||||
| chr5:100558935 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.435-3119A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558935 | |||||||
| chr5:100558955 | G | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-3099G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558955 | |||||||
| chr5:100559128 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(4): Show |
7 | HG02559.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.435-2926G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559128 | |||||||
| chr5:100559172 | T | G | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2882T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559172 | |||||||
| chr5:100559190 | T | C | 47 | a0001c0001t0004g0030 a0001c0001t0004g0249 a0001c0002t0001g0002 others(44): Show |
57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-2864T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559190 | |||||||
| chr5:100559193 | A | T | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-2861A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559193 | |||||||
| chr5:100559223 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.435-2831C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559223 | |||||||
| chr5:100559242 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.435-2812C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559242 | |||||||
| chr5:100559297 | C | T | 1 | a0001c0002t0001g0217 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.435-2757C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559297 | |||||||
| chr5:100559328 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.435-2726C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559328 | |||||||
| chr5:100559344 | G | A | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2710G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559344 | |||||||
| chr5:100559496 | A | G | 1 | a0001c0002t0001g0230 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.435-2558A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559496 | |||||||
| chr5:100559643 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0042 a0001c0001t0003g0044 |
4 | HG01167.hp1 HG01169.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-2411G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559643 | |||||||
| chr5:100559839 | A | T | 27 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(24): Show |
35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.435-2215A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559839 | |||||||
| chr5:100559840 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-2214G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559840 | |||||||
| chr5:100559846 | T | A | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2208T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559846 | |||||||
| chr5:100559846 | T | C | 2 | a0001c0001t0003g0007 a0001c0001t0003g0044 |
3 | HG01167.hp1 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.435-2208T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559846 | |||||||
| chr5:100559928 | G | A | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2126G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559928 | |||||||
| chr5:100560208 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.435-1846G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560208 | |||||||
| chr5:100560256 | A | C | 1 | a0001c0001t0002g0125 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.435-1798A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560256 | |||||||
| chr5:100560267 | A | T | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435-1787A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560267 | |||||||
| chr5:100560414 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
99 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.435-1640C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560414 | |||||||
| chr5:100560490 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.435-1564T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560490 | |||||||
| chr5:100560540 | A | G | 47 | a0001c0001t0004g0030 a0001c0001t0004g0249 a0001c0002t0001g0002 others(44): Show |
57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-1514A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560540 | |||||||
| chr5:100560557 | T | C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-1497T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560557 | |||||||
| chr5:100560730 | T | G | 1 | a0001c0001t0003g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.435-1324T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560730 | |||||||
| chr5:100560864 | C | G | 47 | a0001c0001t0004g0030 a0001c0001t0004g0249 a0001c0002t0001g0002 others(44): Show |
57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-1190C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560864 | |||||||
| chr5:100560920 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.435-1134A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560920 | |||||||
| chr5:100560948 | C | G | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-1106C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560948 | |||||||
| chr5:100561067 | G | T | 1 | a0001c0001t0003g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.435-987G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561067 | |||||||
| chr5:100561471 | T | C | 3 | a0001c0001t0002g0127 a0001c0001t0002g0147 a0001c0001t0002g0148 |
3 | HG00741.hp1 HG01255.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.435-583T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561471 | |||||||
| chr5:100561524 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.435-530T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561524 | |||||||
| chr5:100561634 | A | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-420A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561634 | |||||||
| chr5:100561639 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-415C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561639 | |||||||
| chr5:100561681 | C | T | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-373C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561681 | |||||||
| chr5:100561682 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.435-372G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561682 | |||||||
| chr5:100561768 | C | T | 7 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0120 others(4): Show |
7 | HG02015.hp1 HG02040.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-286C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561768 | |||||||
| chr5:100561769 | G | A | 1 | a0001c0002t0006g0237 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.435-285G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561769 | |||||||
| chr5:100562451 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.569+263G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562451 | |||||||
| chr5:100562468 | T | G | 2 | a0001c0001t0002g0110 a0001c0001t0002g0129 |
2 | HG02027.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.569+280T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562468 | |||||||
| chr5:100562474 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.569+286A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562474 | |||||||
| chr5:100562509 | T | G | 1 | a0001c0001t0002g0146 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.569+321T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562509 | |||||||
| chr5:100562631 | T | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+443T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562631 | |||||||
| chr5:100562633 | A | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.569+445A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562633 | |||||||
| chr5:100562701 | T | C | 11 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0038 others(8): Show |
13 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.569+513T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562701 | |||||||
| chr5:100562984 | G | A | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+796G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562984 | |||||||
| chr5:100562985 | C | T | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+797C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562985 | |||||||
| chr5:100563147 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
63 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.569+959T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563147 | |||||||
| chr5:100563179 | A | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+991A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563179 | |||||||
| chr5:100563250 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.569+1062C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563250 | |||||||
| chr5:100563282 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.569+1094A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563282 | |||||||
| chr5:100563315 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.569+1127A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563315 | |||||||
| chr5:100563339 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.569+1151C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563339 | |||||||
| chr5:100563372 | AT | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+1188delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100563372 | ||||||
| chr5:100563400 | C | CA | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+1224dupA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100563400 | ||||||
| chr5:100563400 | CA | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
98 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.569+1224delA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100563400 | ||||||
| chr5:100563476 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.569+1288G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563476 | |||||||
| chr5:100563614 | G | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.569+1426G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563614 | |||||||
| chr5:100563667 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.569+1479C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563667 | |||||||
| chr5:100563763 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.569+1575T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563763 | |||||||
| chr5:100563986 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.569+1798G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563986 | |||||||
| chr5:100564054 | C | T | 1 | a0001c0001t0002g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.569+1866C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564054 | |||||||
| chr5:100564072 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.569+1884G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564072 | |||||||
| chr5:100564183 | G | A | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.569+1995G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564183 | |||||||
| chr5:100564310 | A | G | 47 | a0001c0001t0004g0030 a0001c0001t0004g0249 a0001c0002t0001g0002 others(44): Show |
57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.569+2122A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564310 | |||||||
| chr5:100564336 | C | CA | 31 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0003g0056 others(28): Show |
39 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.569+2158dupA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100564336 | ||||||
| chr5:100564337 | A | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569+2149A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564337 | |||||||
| chr5:100564350 | C | A | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.569+2162C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564350 | |||||||
| chr5:100564364 | T | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0247 |
4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+2176T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564364 | |||||||
| chr5:100564604 | C | T | 17 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(14): Show |
19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.569+2416C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564604 | |||||||
| chr5:100564695 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.569+2507A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564695 | |||||||
| chr5:100564700 | C | T | 45 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(42): Show |
54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+2512C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564700 | |||||||
| chr5:100564755 | C | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+2567C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564755 | |||||||
| chr5:100564917 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.569+2729G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564917 | |||||||
| chr5:100565094 | T | TA | 64 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(61): Show |
76 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.569+2906_569+2907i others(3): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565094 | |||||||
| chr5:100565113 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.569+2925A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565113 | |||||||
| chr5:100565168 | A | C | 8 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.569+2980A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565168 | |||||||
| chr5:100565518 | A | G | 37 | a0001c0001t0001g0128 a0001c0001t0002g0017 a0001c0001t0002g0018 others(34): Show |
38 | HG00621.hp2 HG01099.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.569+3330A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565518 | |||||||
| chr5:100565607 | A | G | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+3419A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565607 | |||||||
| chr5:100565613 | T | G | 1 | a0001c0001t0002g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.569+3425T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565613 | |||||||
| chr5:100565760 | T | A | 1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.569+3572T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565760 | |||||||
| chr5:100565763 | G | A | 1 | a0001c0002t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.569+3575G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565763 | |||||||
| chr5:100565827 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.569+3639G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565827 | |||||||
| chr5:100565925 | T | C | 2 | a0001c0002t0001g0239 a0001c0002t0001g0243 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.569+3737T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565925 | |||||||
| chr5:100566004 | C | CTT | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+3817_569+3818d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566004 | ||||||
| chr5:100566141 | G | GAT | 22 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0061 others(19): Show |
30 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.569+3982_569+3983d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATAGATA others(1): Show |
2 | a0001c0002t0001g0026 a0001c0002t0001g0231 |
3 | HG01071.hp2 HG01123.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.569+3956_569+3957i others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATAGATA others(5): Show |
2 | a0001c0002t0001g0224 a0001c0002t0001g0234 |
2 | HG01167.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.569+3956_569+3957i others(14): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATAGATA others(7): Show |
4 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0229 others(1): Show |
6 | HG01516.hp2 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+3956_569+3957i others(16): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATAGATA others(9): Show |
5 | a0001c0002t0001g0027 a0001c0002t0001g0218 a0001c0002t0001g0227 others(2): Show |
6 | HG01081.hp2 HG01192.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+3956_569+3957i others(18): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATAGATA others(11): Show |
5 | a0001c0002t0001g0002 a0001c0002t0001g0219 a0001c0002t0001g0230 others(2): Show |
9 | HG00140.hp2 HG00735.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.569+3956_569+3957i others(20): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATAGATA others(13): Show |
3 | a0001c0002t0001g0217 a0001c0002t0001g0226 a0001c0002t0006g0237 |
3 | HG02293.hp2 HG02735.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.569+3956_569+3957i others(22): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATAT | 27 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(24): Show |
29 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.569+3980_569+3983d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATATAT | 33 | a0001c0001t0001g0035 a0001c0001t0001g0068 a0001c0001t0001g0072 others(30): Show |
34 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.569+3978_569+3983d others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATATATA others(1): Show |
33 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(30): Show |
37 | HG00408.hp1 HG01099.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.569+3976_569+3983d others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATATATA others(3): Show |
26 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0070 others(23): Show |
28 | HG00621.hp1 HG01358.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.569+3974_569+3983d others(12): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATATATA others(5): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0016 others(26): Show |
32 | HG00323.hp2 HG00597.hp1 HG02135.hp1 others(29): Show |
intron_variant | MODIFIER | c.569+3972_569+3983d others(14): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATATATA others(7): Show |
22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
28 | HG00099.hp2 HG00280.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.569+3970_569+3983d others(16): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATATATA others(9): Show |
4 | a0001c0001t0001g0073 a0001c0001t0001g0082 a0001c0001t0001g0086 others(1): Show |
4 | HG00621.hp2 HG02015.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+3968_569+3983d others(18): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | G | GATATATA others(13): Show |
2 | a0001c0001t0002g0111 a0001c0001t0002g0253 |
2 | NA19004.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.569+3964_569+3983d others(22): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | GAT | G | 5 | a0001c0001t0002g0125 a0001c0001t0002g0127 a0001c0001t0002g0174 others(2): Show |
5 | HG00642.hp1 HG01243.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+3982_569+3983d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | GATAT | G | 6 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0123 others(3): Show |
7 | HG01934.hp1 HG02015.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.569+3980_569+3983d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | GATATATA others(1): Show |
G | 3 | a0001c0001t0002g0124 a0001c0001t0003g0037 a0001c0001t0003g0045 |
3 | HG02056.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.569+3976_569+3983d others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566141 | GATATATA others(3): Show |
G | 17 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0038 others(14): Show |
20 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.569+3974_569+3983d others(12): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | ||||||
| chr5:100566145 | T | G | 2 | a0001c0001t0002g0179 a0001c0001t0002g0244 |
2 | HG01243.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.569+3957T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566145 | |||||||
| chr5:100566210 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569+4022T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566210 | |||||||
| chr5:100566249 | A | T | 2 | a0001c0001t0002g0151 a0001c0001t0002g0173 |
2 | HG00438.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.569+4061A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566249 | |||||||
| chr5:100566271 | A | G | 3 | a0001c0001t0001g0093 a0001c0002t0001g0254 a0001c0002t0001g0255 |
3 | HG01891.hp2 HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.569+4083A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566271 | |||||||
| chr5:100566307 | TAGAA | T | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0080 others(5): Show |
13 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.569+4123_569+4126d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566307 | ||||||
| chr5:100566479 | G | A | 4 | a0001c0001t0003g0056 a0001c0001t0003g0062 a0001c0001t0003g0063 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+4291G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566479 | |||||||
| chr5:100566500 | G | T | 4 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0233 others(1): Show |
6 | HG01934.hp2 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+4312G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566500 | |||||||
| chr5:100566712 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.569+4524G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566712 | |||||||
| chr5:100566745 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.569+4557C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566745 | |||||||
| chr5:100566828 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.569+4640T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566828 | |||||||
| chr5:100567289 | CAAAT | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0002g0245 others(1): Show |
6 | HG02486.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+5102_569+5105d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567289 | |||||||
| chr5:100567367 | C | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.569+5179C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567367 | |||||||
| chr5:100567404 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.569+5216A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567404 | |||||||
| chr5:100567723 | GT | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
108 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.569+5538delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100567723 | ||||||
| chr5:100567855 | C | T | 1 | a0001c0002t0001g0239 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.569+5667C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567855 | |||||||
| chr5:100567974 | A | G | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+5786A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567974 | |||||||
| chr5:100568024 | G | T | 1 | a0001c0001t0002g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.569+5836G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568024 | |||||||
| chr5:100568198 | A | G | 13 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(10): Show |
15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.569+6010A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568198 | |||||||
| chr5:100568202 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18960.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.569+6014C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568202 | |||||||
| chr5:100568260 | A | T | 8 | a0001c0001t0003g0006 a0001c0001t0003g0038 a0001c0001t0003g0039 others(5): Show |
9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.569+6072A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568260 | |||||||
| chr5:100568536 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+6348C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568536 | |||||||
| chr5:100568592 | T | TTTGTTTT others(17): Show |
2 | a0001c0001t0002g0022 a0001c0001t0002g0191 |
3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6406_569+6407i others(26): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100568592 | ||||||
| chr5:100568597 | A | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0191 |
3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6409A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568597 | |||||||
| chr5:100568599 | A | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0191 |
3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6411A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568599 | |||||||
| chr5:100568601 | T | TTTTGCC | 2 | a0001c0001t0002g0022 a0001c0001t0002g0191 |
3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6414_569+6415i others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100568601 | ||||||
| chr5:100568737 | A | AG | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+6549_569+6550i others(3): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568737 | |||||||
| chr5:100568752 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0002g0245 |
4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+6564G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568752 | |||||||
| chr5:100568789 | A | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0173 |
2 | HG00438.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.569+6601A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568789 | |||||||
| chr5:100568800 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.569+6612G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568800 | |||||||
| chr5:100568828 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+6640G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568828 | |||||||
| chr5:100568830 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0095 |
3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+6642T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568830 | |||||||
| chr5:100568916 | A | AGGTTTCT others(5): Show |
19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+6729_569+6740d others(14): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100568916 | ||||||
| chr5:100568969 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.569+6781A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568969 | |||||||
| chr5:100568987 | A | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+6799A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568987 | |||||||
| chr5:100569065 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0002g0245 |
4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+6877T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569065 | |||||||
| chr5:100569311 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02717.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.569+7123A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569311 | |||||||
| chr5:100569348 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+7160C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569348 | |||||||
| chr5:100569352 | T | A | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+7164T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569352 | |||||||
| chr5:100569387 | A | T | 1 | a0001c0001t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.569+7199A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569387 | |||||||
| chr5:100569391 | T | TTA | 88 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0034 others(85): Show |
106 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(103): Show |
intron_variant | MODIFIER | c.569+7215_569+7216d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100569391 | ||||||
| chr5:100569391 | T | TTATA | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
58 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.569+7213_569+7216d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100569391 | ||||||
| chr5:100569525 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0084 |
2 | HG01358.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.569+7337A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569525 | |||||||
| chr5:100569530 | C | T | 6 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0210 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+7342C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569530 | |||||||
| chr5:100569532 | C | T | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+7344C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569532 | |||||||
| chr5:100569663 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0066 |
3 | HG00099.hp2 HG01192.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.569+7475T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569663 | |||||||
| chr5:100569732 | G | C | 1 | a0001c0001t0002g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.569+7544G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569732 | |||||||
| chr5:100569733 | G | A | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+7545G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569733 | |||||||
| chr5:100569837 | G | GAT | 3 | a0001c0001t0002g0190 a0001c0002t0001g0239 a0001c0002t0001g0243 |
3 | HG02683.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.569+7664_569+7665d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100569837 | ||||||
| chr5:100569854 | C | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0054 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.569+7666C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569854 | |||||||
| chr5:100569925 | G | A | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+7737G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569925 | |||||||
| chr5:100570330 | A | G | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+8142A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570330 | |||||||
| chr5:100570518 | A | C | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+8330A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570518 | |||||||
| chr5:100570559 | G | C | 1 | a0001c0001t0002g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.569+8371G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570559 | |||||||
| chr5:100570675 | G | A | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+8487G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570675 | |||||||
| chr5:100570690 | A | G | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+8502A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570690 | |||||||
| chr5:100570809 | A | G | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.569+8621A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570809 | |||||||
| chr5:100570833 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0095 |
3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+8645G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570833 | |||||||
| chr5:100571143 | TA | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+8956delA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571143 | |||||||
| chr5:100571152 | G | GTA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(94): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.569+8974_569+8975d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571152 | ||||||
| chr5:100571164 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.569+8976G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571164 | |||||||
| chr5:100571262 | G | A | 27 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(24): Show |
35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.569+9074G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571262 | |||||||
| chr5:100571334 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.569+9146G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571334 | |||||||
| chr5:100571365 | A | T | 4 | a0001c0001t0003g0056 a0001c0001t0003g0062 a0001c0001t0003g0063 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+9177A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571365 | |||||||
| chr5:100571386 | G | C | 1 | a0001c0001t0002g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.569+9198G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571386 | |||||||
| chr5:100571444 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.569+9256T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571444 | |||||||
| chr5:100571446 | G | T | 8 | a0001c0001t0003g0006 a0001c0001t0003g0038 a0001c0001t0003g0039 others(5): Show |
9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.569+9258G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571446 | |||||||
| chr5:100571469 | A | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0002g0245 |
4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+9281A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571469 | |||||||
| chr5:100571496 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.569+9308G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571496 | |||||||
| chr5:100571661 | A | AGT | 5 | a0001c0001t0002g0179 a0001c0001t0003g0056 a0001c0001t0003g0062 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+9484_569+9485d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571661 | ||||||
| chr5:100571672 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+9484G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571672 | |||||||
| chr5:100571672 | G | GTA | 63 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
80 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.569+9503_569+9504d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | ||||||
| chr5:100571672 | G | GTATA | 14 | a0001c0001t0001g0034 a0001c0001t0001g0057 a0001c0001t0001g0058 others(11): Show |
15 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.569+9501_569+9504d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | ||||||
| chr5:100571672 | G | GTATATA | 26 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0002t0001g0002 others(23): Show |
32 | HG00140.hp2 HG00735.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.569+9499_569+9504d others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | ||||||
| chr5:100571672 | G | GTATATAT others(1): Show |
9 | a0001c0001t0001g0048 a0001c0002t0001g0026 a0001c0002t0001g0029 others(6): Show |
12 | HG01071.hp2 HG01256.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.569+9497_569+9504d others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | ||||||
| chr5:100571672 | G | GTGTATAT others(3): Show |
2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.569+9485_569+9486i others(12): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | ||||||
| chr5:100571672 | G | GTGTGTA | 10 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0002t0001g0208 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.569+9485_569+9486i others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | ||||||
| chr5:100571691 | T | C | 3 | a0001c0001t0002g0201 a0001c0002t0001g0254 a0001c0002t0001g0255 |
3 | HG01258.hp2 HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.569+9503T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571691 | |||||||
| chr5:100571693 | C | T | 73 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0033 others(70): Show |
90 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.569+9505C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571693 | |||||||
| chr5:100571695 | C | T | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.569+9507C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571695 | |||||||
| chr5:100571754 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.569+9566T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571754 | |||||||
| chr5:100571828 | C | A | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+9640C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571828 | |||||||
| chr5:100571969 | T | C | 1 | a0001c0001t0002g0019 | 2 | NA18941.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.569+9781T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571969 | |||||||
| chr5:100572171 | G | C | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+9983G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572171 | |||||||
| chr5:100572206 | T | G | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+10018T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572206 | |||||||
| chr5:100572215 | CT | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.569+10035delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100572215 | ||||||
| chr5:100572233 | CT | C | 30 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0058 others(27): Show |
31 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.569+10057delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100572233 | ||||||
| chr5:100572247 | C | A | 1 | a0001c0001t0002g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.569+10059C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572247 | |||||||
| chr5:100572250 | CT | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(7): Show |
11 | HG02486.hp1 HG02559.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.569+10074delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100572250 | ||||||
| chr5:100572399 | G | A | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+10211G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572399 | |||||||
| chr5:100572403 | C | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+10215C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572403 | |||||||
| chr5:100572472 | G | A | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+10284G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572472 | |||||||
| chr5:100572498 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+10310G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572498 | |||||||
| chr5:100572504 | C | T | 4 | a0001c0001t0001g0128 a0002c0003t0001g0001 a0002c0003t0001g0064 others(1): Show |
9 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.569+10316C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572504 | |||||||
| chr5:100572520 | C | T | 10 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0002t0001g0208 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.569+10332C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572520 | |||||||
| chr5:100572521 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.569+10333G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572521 | |||||||
| chr5:100572597 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.569+10409C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572597 | |||||||
| chr5:100572619 | A | T | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+10431A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572619 | |||||||
| chr5:100572722 | G | A | 9 | a0001c0001t0003g0056 a0001c0001t0003g0062 a0001c0001t0003g0063 others(6): Show |
11 | HG01167.hp2 HG01884.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.569+10534G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572722 | |||||||
| chr5:100572893 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.569+10705C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572893 | |||||||
| chr5:100573059 | AGT | A | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+10874_569+1087 others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100573059 | ||||||
| chr5:100573076 | T | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+10888T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573076 | |||||||
| chr5:100573129 | T | G | 2 | a0001c0001t0002g0153 a0001c0001t0002g0161 |
2 | NA18945.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.569+10941T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573129 | |||||||
| chr5:100573138 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569+10950G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573138 | |||||||
| chr5:100573153 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0095 |
3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+10965C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573153 | |||||||
| chr5:100573161 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0161 |
2 | NA18945.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.569+10973C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573161 | |||||||
| chr5:100573196 | G | T | 2 | a0001c0002t0001g0254 a0001c0002t0001g0255 |
2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.569+11008G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573196 | |||||||
| chr5:100573255 | A | C | 1 | a0002c0003t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.569+11067A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573255 | |||||||
| chr5:100573334 | A | G | 17 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(14): Show |
19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.569+11146A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573334 | |||||||
| chr5:100573379 | GT | G | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+11195delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100573379 | ||||||
| chr5:100573388 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0095 |
3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+11200C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573388 | |||||||
| chr5:100573425 | T | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+11237T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573425 | |||||||
| chr5:100573691 | T | C | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+11503T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573691 | |||||||
| chr5:100573712 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.569+11524C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573712 | |||||||
| chr5:100573737 | T | C | 2 | a0001c0002t0001g0239 a0001c0002t0001g0243 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.569+11549T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573737 | |||||||
| chr5:100573742 | A | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0060 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+11554A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573742 | |||||||
| chr5:100573760 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0060 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+11572A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573760 | |||||||
| chr5:100573864 | G | T | 4 | a0001c0001t0003g0056 a0001c0001t0003g0062 a0001c0001t0003g0063 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+11676G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573864 | |||||||
| chr5:100573894 | C | T | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG01123.hp1 HG02300.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+11706C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573894 | |||||||
| chr5:100573921 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.569+11733G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573921 | |||||||
| chr5:100574190 | AT | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.570-11983delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100574190 | ||||||
| chr5:100574215 | A | C | 3 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0184 |
3 | HG00280.hp1 HG01106.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.570-11966A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574215 | |||||||
| chr5:100574326 | T | C | 1 | a0001c0001t0002g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570-11855T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574326 | |||||||
| chr5:100574562 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(131): Show |
161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.570-11619G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574562 | |||||||
| chr5:100574584 | A | C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-11597A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574584 | |||||||
| chr5:100574667 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.570-11514T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574667 | |||||||
| chr5:100574717 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570-11464G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574717 | |||||||
| chr5:100574882 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.570-11299C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574882 | |||||||
| chr5:100574911 | C | G | 2 | a0001c0002t0001g0239 a0001c0002t0001g0243 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-11270C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574911 | |||||||
| chr5:100575022 | T | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.570-11159T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575022 | |||||||
| chr5:100575119 | T | C | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-11062T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575119 | |||||||
| chr5:100575217 | C | T | 19 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.570-10964C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575217 | |||||||
| chr5:100575246 | T | TTA | 4 | a0001c0001t0002g0120 a0001c0001t0002g0123 a0001c0001t0002g0168 others(1): Show |
4 | HG01255.hp2 HG02015.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-10921_570-1092 others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100575246 | ||||||
| chr5:100575368 | A | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.570-10813A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575368 | |||||||
| chr5:100575397 | G | A | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(5): Show |
8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.570-10784G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575397 | |||||||
| chr5:100575441 | T | C | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-10740T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575441 | |||||||
| chr5:100575506 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0117 |
2 | NA18971.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.570-10675G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575506 | |||||||
| chr5:100575539 | A | G | 1 | a0001c0002t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570-10642A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575539 | |||||||
| chr5:100575572 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.570-10609A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575572 | |||||||
| chr5:100575605 | A | G | 1 | a0001c0001t0002g0252 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.570-10576A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575605 | |||||||
| chr5:100575659 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.570-10522G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575659 | |||||||
| chr5:100575784 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0002g0245 |
4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.570-10397A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575784 | |||||||
| chr5:100575803 | T | C | 1 | a0001c0001t0002g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.570-10378T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575803 | |||||||
| chr5:100575932 | G | A | 11 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0038 others(8): Show |
13 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.570-10249G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575932 | |||||||
| chr5:100576120 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0090 others(5): Show |
9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-10061C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576120 | |||||||
| chr5:100576151 | C | A | 46 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
55 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.570-10030C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576151 | |||||||
| chr5:100576346 | C | T | 2 | a0001c0002t0001g0239 a0001c0002t0001g0243 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-9835C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576346 | |||||||
| chr5:100576356 | C | T | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-9825C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576356 | |||||||
| chr5:100576379 | T | C | 2 | a0001c0001t0002g0170 a0001c0001t0002g0189 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.570-9802T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576379 | |||||||
| chr5:100576554 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.570-9627G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576554 | |||||||
| chr5:100576702 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0207 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.570-9479A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576702 | |||||||
| chr5:100576738 | A | G | 4 | a0001c0002t0001g0239 a0001c0002t0001g0243 a0001c0002t0001g0254 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.570-9443A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576738 | |||||||
| chr5:100576791 | A | T | 1 | a0001c0001t0002g0121 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.570-9390A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576791 | |||||||
| chr5:100577253 | A | C | 1 | a0001c0001t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.570-8928A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577253 | |||||||
| chr5:100577391 | G | T | 1 | a0001c0001t0002g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.570-8790G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577391 | |||||||
| chr5:100577499 | A | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.570-8682A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577499 | |||||||
| chr5:100577552 | C | T | 6 | a0001c0001t0002g0017 a0001c0001t0002g0100 a0001c0001t0002g0101 others(3): Show |
7 | NA18945.hp1 NA18948.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-8629C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577552 | |||||||
| chr5:100577570 | C | A | 2 | a0001c0002t0001g0239 a0001c0002t0001g0243 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-8611C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577570 | |||||||
| chr5:100577787 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.570-8394A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577787 | |||||||
| chr5:100577857 | T | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-8324T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577857 | |||||||
| chr5:100577916 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.570-8265G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577916 | |||||||
| chr5:100577951 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.570-8230T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577951 | |||||||
| chr5:100578017 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0249 |
3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.570-8164G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578017 | |||||||
| chr5:100578153 | G | C | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.570-8028G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578153 | |||||||
| chr5:100578188 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0176 |
2 | NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.570-7993A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578188 | |||||||
| chr5:100578319 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.570-7862G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578319 | |||||||
| chr5:100578443 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-7738T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578443 | |||||||
| chr5:100578462 | G | A | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-7719G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578462 | |||||||
| chr5:100578530 | C | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-7651C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578530 | |||||||
| chr5:100579032 | A | G | 6 | a0001c0001t0002g0017 a0001c0001t0002g0100 a0001c0001t0002g0101 others(3): Show |
7 | NA18945.hp1 NA18948.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-7149A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579032 | |||||||
| chr5:100579092 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.570-7089T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579092 | |||||||
| chr5:100579171 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.570-7010A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579171 | |||||||
| chr5:100579633 | T | C | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-6548T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579633 | |||||||
| chr5:100579757 | A | T | 1 | a0001c0001t0002g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.570-6424A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579757 | |||||||
| chr5:100580029 | C | T | 8 | a0001c0001t0003g0006 a0001c0001t0003g0038 a0001c0001t0003g0039 others(5): Show |
9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.570-6152C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580029 | |||||||
| chr5:100580168 | A | T | 1 | a0001c0001t0002g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.570-6013A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580168 | |||||||
| chr5:100580188 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0090 others(5): Show |
9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-5993G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580188 | |||||||
| chr5:100580189 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.570-5992C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580189 | |||||||
| chr5:100580234 | A | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0256 |
3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-5947A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580234 | |||||||
| chr5:100580261 | G | GA | 27 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(24): Show |
35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.570-5915dupA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100580261 | ||||||
| chr5:100580268 | G | A | 2 | a0001c0001t0001g0247 a0001c0002t0001g0246 |
2 | HG01255.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.570-5913G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580268 | |||||||
| chr5:100580571 | A | T | 1 | a0001c0001t0001g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.570-5610A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580571 | |||||||
| chr5:100580588 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.570-5593G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580588 | |||||||
| chr5:100580648 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.570-5533C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580648 | |||||||
| chr5:100580762 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.570-5419T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580762 | |||||||
| chr5:100580849 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.570-5332G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580849 | |||||||
| chr5:100580950 | T | G | 1 | a0001c0001t0004g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570-5231T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580950 | |||||||
| chr5:100580980 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0090 others(5): Show |
9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-5201C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580980 | |||||||
| chr5:100581004 | C | G | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.570-5177C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581004 | |||||||
| chr5:100581030 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0207 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.570-5151G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581030 | |||||||
| chr5:100581032 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.570-5149G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581032 | |||||||
| chr5:100581100 | C | G | 20 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(17): Show |
23 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.570-5081C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581100 | |||||||
| chr5:100581323 | A | G | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.570-4858A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581323 | |||||||
| chr5:100581409 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.570-4772G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581409 | |||||||
| chr5:100581556 | C | T | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4625C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581556 | |||||||
| chr5:100581557 | T | G | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4624T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581557 | |||||||
| chr5:100581558 | C | G | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4623C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581558 | |||||||
| chr5:100581559 | G | A | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4622G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581559 | |||||||
| chr5:100581560 | C | A | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4621C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581560 | |||||||
| chr5:100581562 | T | TC | 26 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(23): Show |
27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4619_570-4618i others(3): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581562 | |||||||
| chr5:100581578 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.570-4603T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581578 | |||||||
| chr5:100581891 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0095 |
3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.570-4290T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581891 | |||||||
| chr5:100582350 | A | G | 1 | a0003c0004t0003g0041 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570-3831A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582350 | |||||||
| chr5:100582462 | T | C | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0048 others(6): Show |
9 | HG00741.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-3719T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582462 | |||||||
| chr5:100582474 | GT | G | 12 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(9): Show |
14 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.570-3696delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100582474 | ||||||
| chr5:100582515 | C | T | 45 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(42): Show |
49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-3666C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582515 | |||||||
| chr5:100582897 | C | T | 2 | a0001c0002t0001g0214 a0001c0002t0001g0215 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.570-3284C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582897 | |||||||
| chr5:100583541 | C | T | 1 | a0001c0001t0003g0006 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.570-2640C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583541 | |||||||
| chr5:100583549 | T | A | 17 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0037 others(14): Show |
19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.570-2632T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583549 | |||||||
| chr5:100583638 | AT | A | 15 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(12): Show |
15 | HG00408.hp2 HG01167.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.570-2531delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100583638 | ||||||
| chr5:100583795 | A | G | 36 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0001t0001g0247 others(33): Show |
40 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.570-2386A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583795 | |||||||
| chr5:100583799 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570-2382G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583799 | |||||||
| chr5:100584244 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.570-1937C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584244 | |||||||
| chr5:100584246 | C | G | 10 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0002t0001g0208 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.570-1935C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584246 | |||||||
| chr5:100584322 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.570-1859T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584322 | |||||||
| chr5:100584338 | G | C | 1 | a0001c0001t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570-1843G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584338 | |||||||
| chr5:100584585 | T | G | 2 | a0001c0002t0001g0239 a0001c0002t0001g0243 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-1596T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584585 | |||||||
| chr5:100584601 | G | T | 17 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0001t0001g0247 others(14): Show |
18 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.570-1580G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584601 | |||||||
| chr5:100584680 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.570-1501A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584680 | |||||||
| chr5:100584813 | T | C | 1 | a0001c0002t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.570-1368T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584813 | |||||||
| chr5:100584832 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(94): Show |
120 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.570-1349C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584832 | |||||||
| chr5:100584965 | A | G | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.570-1216A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584965 | |||||||
| chr5:100585242 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.570-939A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585242 | |||||||
| chr5:100585266 | C | T | 1 | a0001c0001t0002g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570-915C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585266 | |||||||
| chr5:100585301 | T | C | 18 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0001t0001g0247 others(15): Show |
19 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.570-880T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585301 | |||||||
| chr5:100585487 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.570-694A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585487 | |||||||
| chr5:100585506 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.570-675C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585506 | |||||||
| chr5:100585563 | G | A | 10 | a0001c0001t0001g0166 a0001c0001t0001g0200 a0001c0002t0001g0208 others(7): Show |
10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.570-618G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585563 | |||||||
| chr5:100585710 | G | A | 1 | a0001c0001t0007g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.570-471G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585710 | |||||||
| chr5:100585731 | A | C | 2 | a0001c0001t0003g0040 a0001c0001t0003g0043 |
2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.570-450A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585731 | |||||||
| chr5:100585781 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.570-400A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585781 | |||||||
| chr5:100585855 | G | A | 1 | a0001c0002t0001g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.570-326G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585855 | |||||||
| chr5:100585878 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0095 |
3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.570-303T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585878 | |||||||
| chr5:100586004 | T | G | 1 | a0001c0001t0003g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.570-177T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100586004 | |||||||
| chr5:100586120 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-61T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100586120 | |||||||
| chr5:100586137 | G | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.570-44G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100586137 |