Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 222234 |
| ensemblid | ENSG00000222011.9 |
| hgncid | 22412 |
| symbol | FAM185A |
| name | family with sequence similarity 185 member A |
| refseq_nuc | NM_001145268.2 |
| refseq_prot | NP_001138740.2 |
| ensembl_nuc | ENST00000413034.3 |
| ensembl_prot | ENSP00000395340.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 102748999 |
| end | 102809225 |
| strand | + |
| ver | v1.2 |
| region | chr7:102748999-102809225 |
| region5000 | chr7:102743999-102814225 |
| regionname0 | FAM185A_chr7_102748999_102809225 |
| regionname5000 | FAM185A_chr7_102743999_102814225 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 392 | 270 | 66 | 38 | 123 | 10 | 33 | 97 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| a0002 | 0/0 | 392 | 46 | 7 | 4 | 30 | 2 | 3 | 21 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| a0003 | 0/1 | 392 | 36 | 9 | 20 | 0 | 3 | 3 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| a0004 | 0/0 | 392 | 18 | 0 | 5 | 9 | 1 | 3 | 6 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| a0005 | 1/0 | 392 | 5 | 4 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| a0006 | 0/0 | 392 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| a0007 | 0/0 | 392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| a0008 | 0/0 | 392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | MLAPC others(387): Show |
chr7 | 102743999 | 102814225 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1176 | 269 | 66 | 38 | 122 | 10 | 33 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0001c0008 | 0/0 | 1176 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0002c0002 | 0/0 | 1176 | 46 | 7 | 4 | 30 | 2 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0003c0003 | 0/1 | 1176 | 36 | 9 | 20 | 0 | 3 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0004c0004 | 0/0 | 1176 | 18 | 0 | 5 | 9 | 1 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0005c0005 | 1/0 | 1176 | 5 | 4 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0006c0006 | 0/0 | 1176 | 3 | 2 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0007c0009 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 | ||
| a0008c0007 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | ATGCT others(1171): Show |
chr7 | 102743999 | 102814225 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2211 | 185 | 54 | 28 | 69 | 9 | 25 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0001t0002 | 0/0 | 2211 | 37 | 0 | 2 | 26 | 1 | 8 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0001t0003 | 0/0 | 2211 | 34 | 0 | 8 | 26 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0001t0004 | 0/0 | 2211 | 6 | 6 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0001t0005 | 0/0 | 2211 | 3 | 3 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0001t0006 | 0/0 | 2211 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0001t0008 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0001t0009 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0001c0008t0001 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0002c0002t0001 | 0/0 | 2211 | 45 | 6 | 4 | 30 | 2 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0002c0002t0004 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0003c0003t0001 | 0/1 | 2211 | 35 | 9 | 20 | 0 | 3 | 2 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0003c0003t0003 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0004c0004t0001 | 0/0 | 2211 | 18 | 0 | 5 | 9 | 1 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0005c0005t0001 | 1/0 | 2211 | 5 | 4 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0006c0006t0001 | 0/0 | 2211 | 3 | 2 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0007c0009t0001 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| a0008c0007t0007 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | AGAGC others(2206): Show |
chr7 | 102743999 | 102814225 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0004 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0001c0008t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0002c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0002 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0003c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0004c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0005c0005t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0005c0005t0001g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0006c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0006c0006t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0006c0006t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0007c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| a0008c0007t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00099 | hp2 | a0004 | c0004 | t0001 | g0278 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0236 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0030 | EUR | FIN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00558 | hp2 | a0004 | c0004 | t0001 | g0273 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00597 | hp2 | a0004 | c0004 | t0001 | g0272 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0085 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0258 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0019 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0063 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0078 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0138 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0019 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0130 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0030 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01175 | hp2 | a0004 | c0004 | t0001 | g0280 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01243 | hp1 | a0006 | c0006 | t0001 | g0263 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0049 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01258 | hp2 | a0003 | c0003 | t0001 | g0147 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0132 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0140 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0237 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0002 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0002 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0154 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01928 | hp1 | a0004 | c0004 | t0001 | g0011 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01978 | hp1 | a0004 | c0004 | t0001 | g0285 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02055 | hp2 | a0006 | c0006 | t0001 | g0251 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02080 | hp2 | a0001 | c0008 | t0001 | g0152 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02135 | hp1 | a0004 | c0004 | t0001 | g0011 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0141 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CDX | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02257 | hp2 | a0007 | c0009 | t0001 | g0026 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0271 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02273 | hp2 | a0004 | c0004 | t0001 | g0031 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02300 | hp1 | a0004 | c0004 | t0001 | g0031 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0139 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0235 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0184 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02723 | hp1 | a0005 | c0005 | t0001 | g0006 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0055 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02886 | hp1 | a0005 | c0005 | t0001 | g0006 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0142 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02922 | hp2 | a0008 | c0007 | t0007 | g0196 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0144 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03209 | hp2 | a0006 | c0006 | t0001 | g0041 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0126 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0224 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0227 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0143 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03710 | hp1 | a0004 | c0004 | t0001 | g0274 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03831 | hp2 | a0003 | c0003 | t0003 | g0127 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03942 | hp2 | a0004 | c0004 | t0001 | g0277 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04184 | hp1 | a0004 | c0004 | t0001 | g0286 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0208 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18951 | hp2 | a0004 | c0004 | t0001 | g0279 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18956 | hp2 | a0004 | c0004 | t0001 | g0282 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18960 | hp2 | a0004 | c0004 | t0001 | g0281 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18966 | hp2 | a0004 | c0004 | t0001 | g0011 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18975 | hp1 | a0001 | c0001 | t0009 | g0201 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18987 | hp1 | a0004 | c0004 | t0001 | g0283 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18993 | hp1 | a0004 | c0004 | t0001 | g0011 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19043 | hp1 | a0005 | c0005 | t0001 | g0006 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | GIH | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | GIH | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0129 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG02486 | hp2 | a0005 | c0005 | t0001 | g0006 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0053 | REF | REF | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| homoSapiens | grch38p0 | a0005 | c0005 | t0001 | g0270 | REF | REF | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:102749250 | C | T | 1 | a0004 | 18 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(15): Show |
missense_variant | MODERATE | c.43C>T | p.Leu15Phe | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 252/2211 | 43/1179 | 15/392 | chr7 | 102749250 | |||
| chr7:102749263 | A | T | 2 | a0002 a0007 |
47 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(44): Show |
missense_variant | MODERATE | c.56A>T | p.Gln19Leu | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 265/2211 | 56/1179 | 19/392 | chr7 | 102749263 | |||
| chr7:102749386 | G | C | 7 | a0001 a0002 a0003 others(4): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
missense_variant | MODERATE | c.179G>C | p.Gly60Ala | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 388/2211 | 179/1179 | 60/392 | chr7 | 102749386 | |||
| chr7:102751766 | A | G | 1 | a0007 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.526A>G | p.Thr176Ala | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/8 | 735/2211 | 526/1179 | 176/392 | chr7 | 102751766 | |||
| chr7:102757921 | T | C | 1 | a0008 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.629T>C | p.Ile210Thr | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/8 | 838/2211 | 629/1179 | 210/392 | chr7 | 102757921 | |||
| chr7:102787442 | C | T | 1 | a0003 | 35 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(32): Show |
missense_variant | MODERATE | c.1039C>T | p.Arg347Cys | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/8 | 1248/2211 | 1039/1179 | 347/392 | chr7 | 102787442 | |||
| chr7:102808372 | T | G | 1 | a0006 | 3 | HG01243.hp1 HG02055.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.1149T>G | p.Ser383Arg | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 1358/2211 | 1149/1179 | 383/392 | chr7 | 102808372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:102777257 | G | A | 1 | a0001c0008 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.840G>A | p.Ser280Ser | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/8 | 1049/2211 | 840/1179 | 280/392 | chr7 | 102777257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:102749077 | T | A | 1 | a0008c0007t0007 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 131 | chr7 | 102749077 | ||||||
| chr7:102749161 | C | T | 1 | a0001c0001t0009 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 47 | chr7 | 102749161 | ||||||
| chr7:102749183 | T | C | 1 | a0001c0001t0008 | 1 | HG01891.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 25 | chr7 | 102749183 | ||||||
| chr7:102808438 | G | T | 2 | a0001c0001t0003 a0003c0003t0003 |
35 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*36G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 36 | chr7 | 102808438 | ||||||
| chr7:102808475 | C | G | 1 | a0001c0001t0006 | 2 | HG03471.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*73C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 73 | chr7 | 102808475 | ||||||
| chr7:102808651 | C | T | 1 | a0001c0001t0005 | 3 | HG02615.hp2 HG02922.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*249C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 249 | chr7 | 102808651 | ||||||
| chr7:102808687 | G | C | 2 | a0001c0001t0004 a0002c0002t0004 |
7 | HG02055.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 285 | chr7 | 102808687 | ||||||
| chr7:102808971 | C | A | 1 | a0001c0001t0002 | 37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 569 | chr7 | 102808971 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:102749729 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0311 a0001c0001t0002g0312 |
5 | HG02015.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+71C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102749729 | |||||||
| chr7:102749819 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(255): Show |
310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.451+161G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102749819 | |||||||
| chr7:102749960 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0002g0265 |
2 | NA18949.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.451+302G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102749960 | |||||||
| chr7:102750310 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451+652G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750310 | |||||||
| chr7:102750538 | T | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG02083.hp1 HG02132.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+880T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750538 | |||||||
| chr7:102750699 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.452-993C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750699 | |||||||
| chr7:102750749 | A | G | 1 | a0006c0006t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.452-943A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750749 | |||||||
| chr7:102750782 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-910G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750782 | |||||||
| chr7:102751006 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452-686C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751006 | |||||||
| chr7:102751074 | C | T | 31 | a0001c0001t0001g0266 a0001c0001t0001g0288 a0001c0001t0001g0293 others(28): Show |
38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.452-618C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751074 | |||||||
| chr7:102751377 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0006g0045 others(1): Show |
4 | HG02109.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-315T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751377 | |||||||
| chr7:102751401 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.452-291C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751401 | |||||||
| chr7:102751450 | ATGTTAGT others(4): Show |
A | 1 | a0001c0001t0001g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.452-240_452-230del others(11): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 102751450 | ||||||
| chr7:102751508 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0259 others(4): Show |
8 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-184C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751508 | |||||||
| chr7:102751527 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
236 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.452-165T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751527 | |||||||
| chr7:102751540 | G | GCTGTGGT others(13): Show |
8 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
8 | HG02080.hp1 HG02698.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-150_452-131dup others(20): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 102751540 | ||||||
| chr7:102751817 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+16A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102751817 | |||||||
| chr7:102751911 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(303): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.561+110C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102751911 | |||||||
| chr7:102752210 | A | T | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.561+409A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752210 | |||||||
| chr7:102752273 | A | AT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(93): Show |
115 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(112): Show |
intron_variant | MODIFIER | c.561+489dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752273 | ||||||
| chr7:102752273 | AT | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0204 others(3): Show |
6 | HG01256.hp1 HG01943.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+489delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752273 | ||||||
| chr7:102752274 | T | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.561+473T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752274 | |||||||
| chr7:102752295 | T | C | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+494T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752295 | |||||||
| chr7:102752421 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+620A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752421 | |||||||
| chr7:102752434 | G | A | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
12 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+633G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752434 | |||||||
| chr7:102752534 | T | C | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
12 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+733T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752534 | |||||||
| chr7:102752577 | A | AT | 22 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0043 others(19): Show |
23 | HG00621.hp1 HG01516.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.561+793dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752577 | ||||||
| chr7:102752577 | AT | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
8 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+793delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752577 | ||||||
| chr7:102752578 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.561+777T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752578 | |||||||
| chr7:102752617 | T | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
236 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.561+816T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752617 | |||||||
| chr7:102752750 | A | T | 7 | a0001c0001t0001g0028 a0001c0001t0004g0246 a0001c0001t0004g0247 others(4): Show |
8 | HG02055.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+949A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752750 | |||||||
| chr7:102752804 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.561+1003T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752804 | |||||||
| chr7:102752874 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0082 others(46): Show |
59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.561+1073A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752874 | |||||||
| chr7:102753136 | A | T | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.561+1335A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753136 | |||||||
| chr7:102753299 | A | T | 2 | a0001c0001t0006g0045 a0001c0001t0006g0046 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.561+1498A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753299 | |||||||
| chr7:102753422 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+1621G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753422 | |||||||
| chr7:102753584 | T | C | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.561+1783T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753584 | |||||||
| chr7:102753626 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.561+1825C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753626 | |||||||
| chr7:102753629 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.561+1828C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753629 | |||||||
| chr7:102753638 | G | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0006g0045 others(1): Show |
4 | HG02109.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+1837G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753638 | |||||||
| chr7:102753741 | C | CA | 106 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0038 others(103): Show |
128 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.561+1951dupA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102753741 | ||||||
| chr7:102753741 | C | CAA | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
12 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+1950_561+1951d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102753741 | ||||||
| chr7:102753881 | T | A | 1 | a0001c0001t0002g0289 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.561+2080T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753881 | |||||||
| chr7:102753911 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
210 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.561+2110C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753911 | |||||||
| chr7:102753968 | G | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(61): Show |
78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.561+2167G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753968 | |||||||
| chr7:102754000 | C | A | 2 | a0001c0001t0002g0290 a0001c0001t0002g0291 |
2 | NA18956.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.561+2199C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754000 | |||||||
| chr7:102754011 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.561+2210G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754011 | |||||||
| chr7:102754204 | AT | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
206 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.561+2417delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102754204 | ||||||
| chr7:102754204 | ATT | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(61): Show |
78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.561+2416_561+2417d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102754204 | ||||||
| chr7:102754206 | T | A | 3 | a0001c0001t0001g0062 a0003c0003t0001g0018 a0003c0003t0001g0126 |
4 | HG01070.hp2 HG01071.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2405T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754206 | |||||||
| chr7:102754224 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0006g0045 others(1): Show |
4 | HG02109.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2423G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754224 | |||||||
| chr7:102754325 | C | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(61): Show |
78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.561+2524C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754325 | |||||||
| chr7:102754604 | A | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(12): Show |
20 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.561+2803A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754604 | |||||||
| chr7:102754639 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(12): Show |
20 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.561+2838C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754639 | |||||||
| chr7:102754640 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+2839G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754640 | |||||||
| chr7:102754738 | A | G | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.561+2937A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754738 | |||||||
| chr7:102754843 | T | C | 1 | a0003c0003t0003g0127 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-3011T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754843 | |||||||
| chr7:102754910 | T | G | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-2944T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754910 | |||||||
| chr7:102755008 | C | T | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-2846C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755008 | |||||||
| chr7:102755125 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.562-2729G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755125 | |||||||
| chr7:102755215 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.562-2639G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755215 | |||||||
| chr7:102755252 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0004g0246 a0001c0001t0004g0247 others(4): Show |
8 | HG02055.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-2602C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755252 | |||||||
| chr7:102755278 | A | G | 2 | a0003c0003t0001g0018 a0003c0003t0001g0126 |
3 | HG01070.hp2 HG01071.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.562-2576A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755278 | |||||||
| chr7:102755382 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.562-2472G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755382 | |||||||
| chr7:102755420 | C | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.562-2434C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755420 | |||||||
| chr7:102755476 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
129 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(126): Show |
intron_variant | MODIFIER | c.562-2378A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755476 | |||||||
| chr7:102755519 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.562-2335C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755519 | |||||||
| chr7:102755596 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0082 others(46): Show |
59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.562-2258C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755596 | |||||||
| chr7:102755609 | T | G | 1 | a0004c0004t0001g0272 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.562-2245T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755609 | |||||||
| chr7:102755610 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.562-2244G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755610 | |||||||
| chr7:102755804 | C | T | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-2050C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755804 | |||||||
| chr7:102755992 | TA | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0082 others(46): Show |
59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.562-1854delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102755992 | ||||||
| chr7:102755993 | A | T | 1 | a0001c0001t0001g0008 | 3 | NA18942.hp2 NA18992.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.562-1861A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755993 | |||||||
| chr7:102756084 | C | A | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
12 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.562-1770C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756084 | |||||||
| chr7:102756096 | C | T | 3 | a0002c0002t0001g0235 a0002c0002t0001g0236 a0002c0002t0001g0237 |
3 | HG00140.hp1 HG01515.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.562-1758C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756096 | |||||||
| chr7:102756121 | A | AT | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-1725dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102756121 | ||||||
| chr7:102756132 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.562-1722C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756132 | |||||||
| chr7:102756540 | C | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
127 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.562-1314C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756540 | |||||||
| chr7:102756605 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.562-1249C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756605 | |||||||
| chr7:102756635 | C | T | 1 | a0001c0001t0005g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.562-1219C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756635 | |||||||
| chr7:102756691 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.562-1163A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756691 | |||||||
| chr7:102756780 | G | A | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.562-1074G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756780 | |||||||
| chr7:102756862 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.562-992C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756862 | |||||||
| chr7:102756914 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
210 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.562-940T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756914 | |||||||
| chr7:102757052 | T | C | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-802T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757052 | |||||||
| chr7:102757297 | T | C | 1 | a0004c0004t0001g0273 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.562-557T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757297 | |||||||
| chr7:102757345 | A | G | 1 | a0002c0002t0001g0234 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.562-509A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757345 | |||||||
| chr7:102757554 | T | A | 1 | a0003c0003t0001g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.562-300T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757554 | |||||||
| chr7:102757813 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0005g0189 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.562-41C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757813 | |||||||
| chr7:102757963 | C | CT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
104 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.654+28dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102757963 | ||||||
| chr7:102757963 | CT | C | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.654+28delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102757963 | ||||||
| chr7:102757971 | T | C | 2 | a0003c0003t0001g0030 a0003c0003t0001g0258 |
3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.654+25T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102757971 | |||||||
| chr7:102758217 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654+271G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758217 | |||||||
| chr7:102758270 | G | T | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.654+324G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758270 | |||||||
| chr7:102758360 | C | A | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
12 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.654+414C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758360 | |||||||
| chr7:102758426 | GC | G | 20 | a0001c0001t0001g0033 a0001c0001t0001g0071 a0001c0001t0001g0146 others(17): Show |
21 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.654+481delC | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | |||||||
| chr7:102758426 | GCT | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0050 others(36): Show |
46 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.654+481_654+482del others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | |||||||
| chr7:102758426 | GCTT | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0020 others(42): Show |
59 | HG00733.hp2 HG01070.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.654+481_654+483del others(3): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | |||||||
| chr7:102758426 | GCTTT | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0064 others(5): Show |
9 | HG01081.hp1 HG01169.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.654+481_654+484del others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | |||||||
| chr7:102758427 | C | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0203 |
2 | HG06807.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.654+481C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758427 | |||||||
| chr7:102758427 | C | T | 2 | a0001c0001t0003g0004 a0001c0001t0003g0097 |
2 | HG02165.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.654+481C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758427 | |||||||
| chr7:102758427 | CT | C | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(34): Show |
44 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.654+513delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTT | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0027 others(45): Show |
55 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.654+512_654+513del others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTTT | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0240 others(48): Show |
58 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.654+511_654+513del others(3): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTTTT | C | 31 | a0001c0001t0001g0275 a0001c0001t0001g0288 a0001c0001t0002g0310 others(28): Show |
34 | HG00544.hp1 HG00597.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.654+510_654+513del others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0056 a0003c0003t0001g0002 a0003c0003t0001g0049 others(1): Show |
8 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+504_654+513del others(10): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG01891.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+503_654+513del others(11): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTTTTTTT others(5): Show |
C | 1 | a0003c0003t0001g0030 | 2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.654+502_654+513del others(12): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0259 a0001c0001t0006g0045 a0001c0001t0006g0046 others(1): Show |
4 | HG00741.hp1 HG01516.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+501_654+513del others(13): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758427 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654+500_654+513del others(14): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | ||||||
| chr7:102758428 | T | A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0071 a0001c0001t0001g0146 others(8): Show |
11 | HG00735.hp2 HG01243.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.654+482T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758428 | |||||||
| chr7:102758429 | T | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0050 others(34): Show |
44 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.654+483T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758429 | |||||||
| chr7:102758430 | T | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0020 others(42): Show |
59 | HG00733.hp2 HG01070.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.654+484T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758430 | |||||||
| chr7:102758431 | T | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0064 others(5): Show |
9 | HG01081.hp1 HG01169.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.654+485T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758431 | |||||||
| chr7:102758435 | T | A | 2 | a0001c0001t0001g0188 a0003c0003t0001g0147 |
2 | HG01258.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.654+489T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758435 | |||||||
| chr7:102758459 | T | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(166): Show |
205 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.654+513T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758459 | |||||||
| chr7:102758514 | C | A | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.654+568C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758514 | |||||||
| chr7:102758708 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.654+762T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758708 | |||||||
| chr7:102758770 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.654+824A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758770 | |||||||
| chr7:102758844 | T | C | 1 | a0004c0004t0001g0274 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.654+898T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758844 | |||||||
| chr7:102758868 | C | CAG | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.654+925_654+926dup others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758868 | ||||||
| chr7:102758995 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0004g0246 a0001c0001t0004g0247 others(4): Show |
8 | HG02055.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+1049C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758995 | |||||||
| chr7:102759092 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.654+1146T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759092 | |||||||
| chr7:102759188 | T | C | 1 | a0001c0001t0002g0292 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.654+1242T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759188 | |||||||
| chr7:102759410 | C | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(61): Show |
78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.654+1464C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759410 | |||||||
| chr7:102759501 | CAT | C | 14 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(11): Show |
19 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.654+1557_654+1558d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102759501 | ||||||
| chr7:102759578 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.654+1632A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759578 | |||||||
| chr7:102759631 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-1642T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759631 | |||||||
| chr7:102759662 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-1611A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759662 | |||||||
| chr7:102759742 | A | C | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-1531A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759742 | |||||||
| chr7:102759836 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0172 |
2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.655-1437C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759836 | |||||||
| chr7:102759977 | G | A | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-1296G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759977 | |||||||
| chr7:102760439 | A | AC | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-834_655-833ins others(1): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760439 | |||||||
| chr7:102760514 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.655-759A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760514 | |||||||
| chr7:102760540 | TCAAA | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(12): Show |
19 | HG00621.hp2 HG01106.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.655-728_655-725del others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102760540 | ||||||
| chr7:102760541 | C | A | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-732C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760541 | |||||||
| chr7:102760685 | A | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
210 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.655-588A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760685 | |||||||
| chr7:102760720 | C | G | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-553C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760720 | |||||||
| chr7:102760731 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.655-542C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760731 | |||||||
| chr7:102760806 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
127 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.655-467G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760806 | |||||||
| chr7:102760903 | A | T | 1 | a0001c0001t0002g0310 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.655-370A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760903 | |||||||
| chr7:102760966 | C | T | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
12 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.655-307C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760966 | |||||||
| chr7:102760986 | A | G | 1 | a0002c0002t0001g0237 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.655-287A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760986 | |||||||
| chr7:102761107 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.655-166C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102761107 | |||||||
| chr7:102761124 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.655-149G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102761124 | |||||||
| chr7:102761537 | C | CT | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0058 others(3): Show |
6 | HG02109.hp2 HG03139.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+131dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102761537 | ||||||
| chr7:102761542 | T | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0238 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793+131T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761542 | |||||||
| chr7:102761542 | TA | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0082 others(46): Show |
59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.793+142delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102761542 | ||||||
| chr7:102761543 | A | T | 9 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0259 others(6): Show |
14 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.793+132A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761543 | |||||||
| chr7:102761628 | A | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0260 |
3 | NA18990.hp1 NA18994.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.793+217A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761628 | |||||||
| chr7:102761678 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.793+267T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761678 | |||||||
| chr7:102761800 | A | T | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+389A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761800 | |||||||
| chr7:102761813 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.793+402G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761813 | |||||||
| chr7:102761939 | A | G | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+528A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761939 | |||||||
| chr7:102762093 | T | G | 4 | a0003c0003t0001g0019 a0003c0003t0001g0063 a0003c0003t0001g0130 others(1): Show |
5 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+682T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762093 | |||||||
| chr7:102762115 | G | C | 2 | a0001c0001t0006g0045 a0001c0001t0006g0046 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.793+704G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762115 | |||||||
| chr7:102762163 | T | C | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+752T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762163 | |||||||
| chr7:102762183 | T | A | 1 | a0001c0001t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.793+772T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762183 | |||||||
| chr7:102762183 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.793+772T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762183 | |||||||
| chr7:102762229 | T | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0056 others(12): Show |
20 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.793+818T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762229 | |||||||
| chr7:102762339 | G | A | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+928G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762339 | |||||||
| chr7:102762684 | T | G | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+1273T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762684 | |||||||
| chr7:102762810 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.793+1399C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762810 | |||||||
| chr7:102762830 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.793+1419T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762830 | |||||||
| chr7:102762851 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.793+1440A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762851 | |||||||
| chr7:102762923 | A | G | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+1512A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762923 | |||||||
| chr7:102763317 | T | A | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.793+1906T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763317 | |||||||
| chr7:102763343 | T | TG | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.793+1934dupG | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102763343 | ||||||
| chr7:102763580 | G | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0066 others(16): Show |
27 | HG02040.hp1 HG02071.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.793+2169G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763580 | |||||||
| chr7:102763817 | G | C | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.793+2406G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763817 | |||||||
| chr7:102763831 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.793+2420C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763831 | |||||||
| chr7:102763906 | T | C | 46 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(43): Show |
54 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.793+2495T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763906 | |||||||
| chr7:102764004 | T | C | 1 | a0001c0008t0001g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.793+2593T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764004 | |||||||
| chr7:102764141 | G | C | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.793+2730G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764141 | |||||||
| chr7:102764340 | A | G | 47 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(44): Show |
55 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.793+2929A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764340 | |||||||
| chr7:102764407 | G | T | 2 | a0003c0003t0001g0030 a0003c0003t0001g0258 |
3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+2996G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764407 | |||||||
| chr7:102764621 | C | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(6): Show |
9 | HG02080.hp1 HG02698.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+3210C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764621 | |||||||
| chr7:102764665 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0238 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793+3254A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764665 | |||||||
| chr7:102764749 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0183 a0001c0001t0001g0188 |
3 | HG03704.hp1 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.793+3338G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764749 | |||||||
| chr7:102764827 | GA | G | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0008g0054 others(3): Show |
10 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+3426delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102764827 | ||||||
| chr7:102764848 | A | G | 35 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0001g0094 others(32): Show |
42 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.793+3437A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764848 | |||||||
| chr7:102764893 | T | G | 3 | a0003c0003t0001g0153 a0003c0003t0001g0154 a0003c0003t0001g0184 |
3 | HG01884.hp2 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.793+3482T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764893 | |||||||
| chr7:102764898 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.793+3487T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764898 | |||||||
| chr7:102764933 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.793+3522T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764933 | |||||||
| chr7:102765195 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.793+3784C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765195 | |||||||
| chr7:102765346 | G | A | 2 | a0001c0001t0003g0093 a0001c0001t0003g0123 |
2 | HG00621.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.793+3935G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765346 | |||||||
| chr7:102765395 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.793+3984G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765395 | |||||||
| chr7:102765471 | G | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0105 a0001c0001t0001g0106 others(4): Show |
9 | NA18941.hp2 NA18945.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+4060G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765471 | |||||||
| chr7:102765482 | A | T | 41 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(38): Show |
47 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.793+4071A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765482 | |||||||
| chr7:102765829 | C | T | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+4418C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765829 | |||||||
| chr7:102765830 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0117 |
2 | NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.793+4419G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765830 | |||||||
| chr7:102765885 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793+4474T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765885 | |||||||
| chr7:102765943 | A | G | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.793+4532A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765943 | |||||||
| chr7:102765947 | GAAT | G | 4 | a0003c0003t0001g0153 a0003c0003t0001g0154 a0003c0003t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+4541_793+4543d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102765947 | ||||||
| chr7:102765951 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0180 |
2 | HG01433.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.793+4540A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765951 | |||||||
| chr7:102765967 | C | A | 6 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(3): Show |
6 | HG02055.hp1 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+4556C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765967 | |||||||
| chr7:102765988 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.793+4577T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765988 | |||||||
| chr7:102765992 | C | T | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+4581C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765992 | |||||||
| chr7:102766001 | C | T | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0059 others(5): Show |
9 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.793+4590C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766001 | |||||||
| chr7:102766046 | A | G | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.793+4635A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766046 | |||||||
| chr7:102766123 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0067 others(1): Show |
8 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+4712G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766123 | |||||||
| chr7:102766230 | G | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02080.hp1 HG02698.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+4819G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766230 | |||||||
| chr7:102766554 | G | C | 1 | a0001c0001t0004g0246 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793+5143G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766554 | |||||||
| chr7:102766619 | A | AAC | 90 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(87): Show |
100 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.793+5210_793+5211d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766619 | ||||||
| chr7:102766674 | T | G | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+5263T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766674 | |||||||
| chr7:102766771 | CTTTGTTT others(2): Show |
C | 3 | a0001c0001t0005g0189 a0001c0001t0006g0045 a0001c0001t0006g0046 |
3 | HG02922.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.793+5378_793+5386d others(11): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766771 | ||||||
| chr7:102766775 | G | GT | 19 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(16): Show |
23 | HG00544.hp1 HG00621.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.793+5372dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766775 | ||||||
| chr7:102766784 | G | GT | 8 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0064 others(5): Show |
10 | HG00733.hp2 HG01261.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+5381dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766784 | ||||||
| chr7:102766789 | T | G | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+5378T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766789 | |||||||
| chr7:102766854 | G | A | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+5443G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766854 | |||||||
| chr7:102766940 | G | A | 23 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0038 others(20): Show |
25 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.794-5469G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766940 | |||||||
| chr7:102766955 | T | C | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.794-5454T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766955 | |||||||
| chr7:102766986 | G | T | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.794-5423G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766986 | |||||||
| chr7:102767022 | C | T | 3 | a0003c0003t0001g0133 a0003c0003t0001g0143 a0003c0003t0001g0144 |
3 | HG02717.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.794-5387C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767022 | |||||||
| chr7:102767038 | C | T | 1 | a0001c0001t0002g0307 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-5371C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767038 | |||||||
| chr7:102767041 | A | G | 1 | a0002c0002t0004g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.794-5368A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767041 | |||||||
| chr7:102767042 | C | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(35): Show |
41 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.794-5367C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767042 | |||||||
| chr7:102767043 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.794-5366G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767043 | |||||||
| chr7:102767073 | G | C | 43 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(40): Show |
49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.794-5336G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767073 | |||||||
| chr7:102767130 | A | G | 9 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0252 others(6): Show |
10 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.794-5279A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767130 | |||||||
| chr7:102767134 | C | CT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.794-5261dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102767134 | ||||||
| chr7:102767134 | C | CTT | 51 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0094 others(48): Show |
57 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.794-5262_794-5261d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102767134 | ||||||
| chr7:102767134 | C | CTTT | 36 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(33): Show |
40 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.794-5263_794-5261d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102767134 | ||||||
| chr7:102767431 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(18): Show |
25 | HG00544.hp1 HG00621.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.794-4978G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767431 | |||||||
| chr7:102767442 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.794-4967C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767442 | |||||||
| chr7:102767560 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.794-4849A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767560 | |||||||
| chr7:102767562 | T | C | 26 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0038 others(23): Show |
29 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.794-4847T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767562 | |||||||
| chr7:102767576 | A | C | 45 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0128 others(42): Show |
51 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.794-4833A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767576 | |||||||
| chr7:102767833 | C | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0174 others(5): Show |
8 | HG02109.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-4576C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767833 | |||||||
| chr7:102767988 | T | G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0145 others(2): Show |
5 | HG01106.hp1 HG02717.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-4421T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767988 | |||||||
| chr7:102767989 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(241): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.794-4420A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767989 | |||||||
| chr7:102768007 | T | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0252 others(3): Show |
8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-4402T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768007 | |||||||
| chr7:102768019 | T | C | 30 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0087 others(27): Show |
36 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.794-4390T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768019 | |||||||
| chr7:102768119 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0024 others(59): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.794-4290T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768119 | |||||||
| chr7:102768135 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.794-4274C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768135 | |||||||
| chr7:102768193 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.794-4216C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768193 | |||||||
| chr7:102768451 | T | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(304): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.794-3958T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768451 | |||||||
| chr7:102768535 | T | C | 4 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0212 others(1): Show |
5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-3874T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768535 | |||||||
| chr7:102768731 | G | T | 1 | a0003c0003t0001g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.794-3678G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768731 | |||||||
| chr7:102768961 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(164): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.794-3448C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768961 | |||||||
| chr7:102769024 | G | A | 123 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(120): Show |
145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.794-3385G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769024 | |||||||
| chr7:102769075 | G | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0089 others(1): Show |
4 | HG02257.hp1 HG03239.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-3334G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769075 | |||||||
| chr7:102769437 | T | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(299): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.794-2972T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769437 | |||||||
| chr7:102769477 | G | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2932G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769477 | |||||||
| chr7:102769489 | A | C | 1 | a0003c0003t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.794-2920A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769489 | |||||||
| chr7:102769541 | G | A | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2868G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769541 | |||||||
| chr7:102769649 | A | G | 28 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(25): Show |
30 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.794-2760A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769649 | |||||||
| chr7:102769765 | T | C | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.794-2644T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769765 | |||||||
| chr7:102769919 | C | T | 1 | a0002c0002t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.794-2490C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769919 | |||||||
| chr7:102770030 | C | G | 29 | a0001c0001t0005g0276 a0001c0001t0005g0284 a0003c0003t0001g0002 others(26): Show |
36 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.794-2379C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770030 | |||||||
| chr7:102770056 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.794-2353G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770056 | |||||||
| chr7:102770219 | T | C | 1 | a0001c0001t0004g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.794-2190T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770219 | |||||||
| chr7:102770380 | G | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.794-2029G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770380 | |||||||
| chr7:102770418 | G | A | 2 | a0001c0001t0006g0045 a0001c0001t0006g0046 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.794-1991G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770418 | |||||||
| chr7:102770619 | G | C | 1 | a0001c0001t0003g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.794-1790G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770619 | |||||||
| chr7:102770901 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.794-1508T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770901 | |||||||
| chr7:102771024 | G | A | 58 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(55): Show |
64 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.794-1385G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771024 | |||||||
| chr7:102771769 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.794-640C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771769 | |||||||
| chr7:102771866 | A | G | 2 | a0001c0001t0001g0077 a0004c0004t0001g0285 |
2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.794-543A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771866 | |||||||
| chr7:102771914 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.794-495C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771914 | |||||||
| chr7:102771964 | T | C | 30 | a0001c0001t0005g0276 a0001c0001t0005g0284 a0003c0003t0001g0002 others(27): Show |
37 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.794-445T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771964 | |||||||
| chr7:102772199 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | NA18942.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.794-210G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102772199 | |||||||
| chr7:102772233 | C | A | 1 | a0006c0006t0001g0263 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.794-176C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102772233 | |||||||
| chr7:102772842 | A | G | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.835+392A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102772842 | |||||||
| chr7:102772953 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.835+503C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102772953 | |||||||
| chr7:102773100 | G | C | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.835+650G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773100 | |||||||
| chr7:102773259 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+809G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773259 | |||||||
| chr7:102773332 | A | C | 1 | a0001c0001t0002g0081 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835+882A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773332 | |||||||
| chr7:102773426 | A | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0042 others(55): Show |
69 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.835+976A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773426 | |||||||
| chr7:102773467 | C | T | 1 | a0002c0002t0001g0230 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.835+1017C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773467 | |||||||
| chr7:102773532 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.835+1082T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773532 | |||||||
| chr7:102773539 | G | A | 1 | a0004c0004t0001g0281 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.835+1089G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773539 | |||||||
| chr7:102773580 | G | A | 4 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0212 others(1): Show |
5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+1130G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773580 | |||||||
| chr7:102773860 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.835+1410G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773860 | |||||||
| chr7:102774151 | G | A | 141 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0028 others(138): Show |
167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.835+1701G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774151 | |||||||
| chr7:102774163 | G | C | 126 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(123): Show |
148 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.835+1713G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774163 | |||||||
| chr7:102774258 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG02970.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.835+1808T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774258 | |||||||
| chr7:102774305 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.835+1855T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774305 | |||||||
| chr7:102774436 | C | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+1986C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774436 | |||||||
| chr7:102774640 | T | C | 1 | a0001c0001t0004g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.835+2190T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774640 | |||||||
| chr7:102774680 | T | G | 1 | a0001c0001t0002g0287 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.835+2230T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774680 | |||||||
| chr7:102775010 | G | GT | 47 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(44): Show |
57 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-2231dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102775010 | ||||||
| chr7:102775016 | T | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0181 |
2 | HG02165.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.836-2237T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775016 | |||||||
| chr7:102775145 | A | G | 34 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0192 others(31): Show |
41 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.836-2108A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775145 | |||||||
| chr7:102775296 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.836-1957T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775296 | |||||||
| chr7:102775696 | CTAA | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.836-1555_836-1553d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102775696 | ||||||
| chr7:102775780 | A | G | 4 | a0003c0003t0001g0153 a0003c0003t0001g0154 a0003c0003t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-1473A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775780 | |||||||
| chr7:102775807 | C | T | 144 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0028 others(141): Show |
170 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.836-1446C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775807 | |||||||
| chr7:102775965 | G | C | 1 | a0001c0001t0003g0098 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.836-1288G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775965 | |||||||
| chr7:102775982 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.836-1271T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775982 | |||||||
| chr7:102776015 | C | T | 2 | a0002c0002t0001g0228 a0002c0002t0001g0229 |
2 | HG00597.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.836-1238C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102776015 | |||||||
| chr7:102776046 | CTCTT | C | 62 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(59): Show |
69 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.836-1205_836-1202d others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776046 | ||||||
| chr7:102776099 | T | TACACACA others(21): Show |
1 | a0001c0001t0004g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | ||||||
| chr7:102776099 | T | TACACACA others(19): Show |
7 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0004g0246 others(4): Show |
7 | HG02055.hp1 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(28): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | ||||||
| chr7:102776099 | T | TACACACA others(21): Show |
2 | a0002c0002t0001g0207 a0002c0002t0004g0208 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | ||||||
| chr7:102776099 | T | TACACACA others(23): Show |
1 | a0002c0002t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.836-1137_836-1136i others(32): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | ||||||
| chr7:102776099 | T | TACACACA others(17): Show |
48 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(45): Show |
59 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(26): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | ||||||
| chr7:102776099 | T | TACACACA others(19): Show |
94 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0028 others(91): Show |
115 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(28): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | ||||||
| chr7:102776099 | T | TACACACA others(21): Show |
47 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0082 others(44): Show |
52 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | ||||||
| chr7:102776111 | C | CACACACA others(21): Show |
1 | a0004c0004t0001g0282 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776111 | ||||||
| chr7:102776170 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.836-1083C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102776170 | |||||||
| chr7:102776190 | C | T | 1 | a0003c0003t0001g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.836-1063C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102776190 | |||||||
| chr7:102776702 | T | TAAAAAA | 61 | a0001c0001t0001g0028 a0001c0001t0001g0084 a0001c0001t0001g0104 others(58): Show |
76 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.836-539_836-534dup others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776702 | ||||||
| chr7:102776702 | T | TAAAAAAA | 48 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(45): Show |
52 | HG00140.hp1 HG00597.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.836-540_836-534dup others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776702 | ||||||
| chr7:102776702 | T | TAAAAAAA others(1): Show |
13 | a0001c0001t0001g0082 a0001c0001t0001g0105 a0001c0001t0001g0106 others(10): Show |
16 | HG00408.hp1 HG01934.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.836-541_836-534dup others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776702 | ||||||
| chr7:102777034 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0195 |
2 | NA18989.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.836-219A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102777034 | |||||||
| chr7:102777094 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.836-159G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102777094 | |||||||
| chr7:102777218 | G | GAATTATT others(309): Show |
1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.836-26_836-25insTT others(314): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102777218 | ||||||
| chr7:102777362 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.931+14A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777362 | |||||||
| chr7:102777674 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0204 a0001c0001t0001g0238 others(1): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+326A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777674 | |||||||
| chr7:102777724 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.931+376G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777724 | |||||||
| chr7:102777770 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.931+422T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777770 | |||||||
| chr7:102777978 | G | T | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.931+630G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777978 | |||||||
| chr7:102778069 | A | T | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.931+721A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778069 | |||||||
| chr7:102778140 | G | A | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.931+792G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778140 | |||||||
| chr7:102778500 | CA | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+1155delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102778500 | ||||||
| chr7:102778509 | T | C | 32 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0295 others(29): Show |
39 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.931+1161T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778509 | |||||||
| chr7:102778609 | G | A | 32 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0295 others(29): Show |
39 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.931+1261G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778609 | |||||||
| chr7:102778857 | C | A | 203 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(200): Show |
237 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.931+1509C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778857 | |||||||
| chr7:102778859 | C | T | 2 | a0003c0003t0001g0002 a0003c0003t0001g0049 |
6 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.931+1511C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778859 | |||||||
| chr7:102778894 | G | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0172 |
2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.931+1546G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778894 | |||||||
| chr7:102779172 | A | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+1824A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779172 | |||||||
| chr7:102779206 | T | C | 1 | a0002c0002t0001g0223 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+1858T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779206 | |||||||
| chr7:102779291 | G | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.931+1943G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779291 | |||||||
| chr7:102779358 | A | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(202): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.931+2010A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779358 | |||||||
| chr7:102779642 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.931+2294T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779642 | |||||||
| chr7:102779850 | C | CT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0268 others(3): Show |
9 | HG01175.hp2 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.931+2531dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | ||||||
| chr7:102779850 | CT | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.931+2531delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | ||||||
| chr7:102779850 | CTT | C | 101 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(98): Show |
123 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.931+2530_931+2531d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | ||||||
| chr7:102779850 | CTTT | C | 12 | a0001c0001t0001g0062 a0001c0001t0001g0076 a0001c0001t0001g0136 others(9): Show |
12 | HG01975.hp2 HG02015.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+2529_931+2531d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | ||||||
| chr7:102779850 | CTTTT | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0061 others(12): Show |
16 | HG01891.hp2 HG02145.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.931+2528_931+2531d others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | ||||||
| chr7:102779850 | CTTTTT | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0038 others(48): Show |
62 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.931+2527_931+2531d others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | ||||||
| chr7:102779850 | CTTTTTT | C | 7 | a0001c0001t0004g0246 a0001c0001t0004g0247 a0001c0001t0004g0248 others(4): Show |
7 | HG01256.hp1 HG02055.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2526_931+2531d others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | ||||||
| chr7:102779980 | A | G | 204 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(201): Show |
238 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.931+2632A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779980 | |||||||
| chr7:102780027 | T | A | 3 | a0001c0001t0005g0189 a0001c0001t0005g0276 a0001c0001t0005g0284 |
3 | HG02615.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.931+2679T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780027 | |||||||
| chr7:102780186 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+2838C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780186 | |||||||
| chr7:102780254 | A | T | 205 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(202): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.931+2906A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780254 | |||||||
| chr7:102780277 | A | G | 2 | a0002c0002t0001g0207 a0002c0002t0004g0208 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.931+2929A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780277 | |||||||
| chr7:102780358 | T | G | 207 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(204): Show |
241 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.931+3010T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780358 | |||||||
| chr7:102780728 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.931+3380C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780728 | |||||||
| chr7:102780826 | C | A | 62 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0038 others(59): Show |
73 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.931+3478C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780826 | |||||||
| chr7:102780836 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.931+3488C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780836 | |||||||
| chr7:102780858 | G | A | 1 | a0002c0002t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+3510G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780858 | |||||||
| chr7:102780901 | C | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(43): Show |
57 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.931+3553C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780901 | |||||||
| chr7:102780990 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.931+3642G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780990 | |||||||
| chr7:102781061 | T | C | 129 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0036 others(126): Show |
151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.931+3713T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781061 | |||||||
| chr7:102781133 | G | A | 2 | a0001c0001t0005g0276 a0001c0001t0005g0284 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.931+3785G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781133 | |||||||
| chr7:102781345 | G | C | 124 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(121): Show |
146 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.931+3997G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781345 | |||||||
| chr7:102781509 | C | T | 2 | a0003c0003t0001g0030 a0003c0003t0001g0258 |
3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.931+4161C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781509 | |||||||
| chr7:102781796 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.931+4448A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781796 | |||||||
| chr7:102781820 | C | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.931+4472C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781820 | |||||||
| chr7:102781985 | G | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0042 others(51): Show |
65 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.931+4637G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781985 | |||||||
| chr7:102781985 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.931+4637G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781985 | |||||||
| chr7:102782136 | A | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0042 others(53): Show |
67 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.931+4788A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782136 | |||||||
| chr7:102782252 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.931+4904C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782252 | |||||||
| chr7:102782306 | A | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+4958A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782306 | |||||||
| chr7:102782318 | C | T | 1 | a0003c0003t0001g0184 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.931+4970C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782318 | |||||||
| chr7:102782430 | C | A | 2 | a0002c0002t0001g0217 a0002c0002t0001g0220 |
2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.932-4905C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782430 | |||||||
| chr7:102782499 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.932-4836C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782499 | |||||||
| chr7:102782500 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0058 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.932-4835G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782500 | |||||||
| chr7:102782567 | A | G | 207 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(204): Show |
241 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.932-4768A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782567 | |||||||
| chr7:102782624 | C | T | 3 | a0001c0001t0001g0160 a0004c0004t0001g0272 a0004c0004t0001g0279 |
3 | HG00597.hp2 HG01070.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.932-4711C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782624 | |||||||
| chr7:102782673 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.932-4662C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782673 | |||||||
| chr7:102782810 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.932-4525T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782810 | |||||||
| chr7:102782902 | A | G | 3 | a0003c0003t0001g0133 a0003c0003t0001g0143 a0003c0003t0001g0144 |
3 | HG02717.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.932-4433A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782902 | |||||||
| chr7:102782912 | C | T | 128 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0036 others(125): Show |
150 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.932-4423C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782912 | |||||||
| chr7:102782972 | A | C | 1 | a0001c0001t0003g0117 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.932-4363A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782972 | |||||||
| chr7:102782977 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.932-4358A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782977 | |||||||
| chr7:102783171 | G | A | 125 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0036 others(122): Show |
147 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.932-4164G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783171 | |||||||
| chr7:102783192 | A | G | 1 | a0004c0004t0001g0283 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.932-4143A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783192 | |||||||
| chr7:102783229 | T | C | 129 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0036 others(126): Show |
151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.932-4106T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783229 | |||||||
| chr7:102783241 | C | T | 2 | a0002c0002t0001g0231 a0003c0003t0001g0140 |
2 | HG01433.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.932-4094C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783241 | |||||||
| chr7:102783325 | A | G | 2 | a0002c0002t0001g0026 a0007c0009t0001g0026 |
2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.932-4010A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783325 | |||||||
| chr7:102783366 | C | T | 1 | a0003c0003t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.932-3969C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783366 | |||||||
| chr7:102783476 | AG | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.932-3858delG | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783476 | |||||||
| chr7:102783600 | A | C | 29 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0003g0004 others(26): Show |
36 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.932-3735A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783600 | |||||||
| chr7:102783619 | C | CATACCAG others(19): Show |
11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-3695_932-3670d others(28): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102783619 | ||||||
| chr7:102783677 | G | C | 208 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(205): Show |
242 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.932-3658G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783677 | |||||||
| chr7:102783801 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.932-3534A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783801 | |||||||
| chr7:102783842 | A | G | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.932-3493A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783842 | |||||||
| chr7:102783889 | G | C | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-3446G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783889 | |||||||
| chr7:102783931 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0188 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.932-3404C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783931 | |||||||
| chr7:102783994 | A | G | 1 | a0001c0001t0002g0300 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.932-3341A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783994 | |||||||
| chr7:102783997 | G | C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0311 a0001c0001t0002g0312 |
5 | HG02015.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-3338G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783997 | |||||||
| chr7:102784009 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.932-3326C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784009 | |||||||
| chr7:102784140 | G | C | 1 | a0002c0002t0001g0218 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.932-3195G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784140 | |||||||
| chr7:102784144 | A | T | 30 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(27): Show |
32 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.932-3191A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784144 | |||||||
| chr7:102784211 | A | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-3124A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784211 | |||||||
| chr7:102784387 | G | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0042 others(51): Show |
65 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.932-2948G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784387 | |||||||
| chr7:102784405 | C | G | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.932-2930C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784405 | |||||||
| chr7:102784448 | A | C | 65 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(62): Show |
72 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.932-2887A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784448 | |||||||
| chr7:102784457 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-2878C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784457 | |||||||
| chr7:102784485 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.932-2850A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784485 | |||||||
| chr7:102784512 | T | C | 131 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(128): Show |
153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-2823T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784512 | |||||||
| chr7:102784573 | C | T | 16 | a0001c0001t0001g0082 a0001c0001t0001g0105 a0001c0001t0001g0106 others(13): Show |
19 | HG00408.hp1 HG01934.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.932-2762C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784573 | |||||||
| chr7:102784605 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.932-2730C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784605 | |||||||
| chr7:102784636 | T | C | 131 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(128): Show |
153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-2699T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784636 | |||||||
| chr7:102784707 | C | G | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-2628C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784707 | |||||||
| chr7:102784721 | A | G | 1 | a0001c0001t0008g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.932-2614A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784721 | |||||||
| chr7:102784772 | C | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-2563C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784772 | |||||||
| chr7:102784922 | A | G | 1 | a0001c0001t0003g0108 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.932-2413A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784922 | |||||||
| chr7:102784938 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0002g0299 |
2 | HG02698.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.932-2397C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784938 | |||||||
| chr7:102784977 | C | A | 2 | a0002c0002t0001g0224 a0002c0002t0001g0227 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.932-2358C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784977 | |||||||
| chr7:102785031 | T | C | 131 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(128): Show |
153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-2304T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785031 | |||||||
| chr7:102785044 | CAG | C | 28 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0019 others(25): Show |
35 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.932-2286_932-2285d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102785044 | ||||||
| chr7:102785090 | G | C | 31 | a0001c0001t0001g0113 a0001c0001t0001g0295 a0001c0001t0002g0007 others(28): Show |
38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.932-2245G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785090 | |||||||
| chr7:102785126 | C | T | 4 | a0003c0003t0001g0019 a0003c0003t0001g0063 a0003c0003t0001g0130 others(1): Show |
5 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-2209C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785126 | |||||||
| chr7:102785311 | C | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0090 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.932-2024C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785311 | |||||||
| chr7:102785331 | T | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(44): Show |
58 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.932-2004T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785331 | |||||||
| chr7:102785366 | C | T | 8 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.932-1969C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785366 | |||||||
| chr7:102785375 | A | G | 132 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(129): Show |
154 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.932-1960A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785375 | |||||||
| chr7:102785398 | C | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG03491.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.932-1937C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785398 | |||||||
| chr7:102785410 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-1925C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785410 | |||||||
| chr7:102785509 | C | T | 2 | a0002c0002t0001g0217 a0002c0002t0001g0220 |
2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.932-1826C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785509 | |||||||
| chr7:102785533 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.932-1802A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785533 | |||||||
| chr7:102785589 | C | G | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.932-1746C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785589 | |||||||
| chr7:102785635 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-1700A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785635 | |||||||
| chr7:102785659 | T | C | 209 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(206): Show |
243 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.932-1676T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785659 | |||||||
| chr7:102785754 | C | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-1581C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785754 | |||||||
| chr7:102785783 | G | T | 2 | a0004c0004t0001g0278 a0004c0004t0001g0286 |
2 | HG00099.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.932-1552G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785783 | |||||||
| chr7:102785814 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.932-1521G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785814 | |||||||
| chr7:102785888 | C | G | 1 | a0001c0001t0001g0266 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.932-1447C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785888 | |||||||
| chr7:102786103 | G | C | 4 | a0003c0003t0001g0153 a0003c0003t0001g0154 a0003c0003t0001g0184 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1232G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786103 | |||||||
| chr7:102786157 | C | T | 29 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0003g0004 others(26): Show |
36 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.932-1178C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786157 | |||||||
| chr7:102786167 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.932-1168A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786167 | |||||||
| chr7:102786320 | C | T | 2 | a0003c0003t0001g0018 a0003c0003t0001g0126 |
3 | HG01070.hp2 HG01071.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.932-1015C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786320 | |||||||
| chr7:102786407 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
7 | HG01891.hp1 HG02572.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-928T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786407 | |||||||
| chr7:102786427 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.932-908C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786427 | |||||||
| chr7:102786439 | A | C | 3 | a0003c0003t0001g0002 a0003c0003t0001g0049 a0003c0003t0001g0055 |
7 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-896A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786439 | |||||||
| chr7:102786572 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.932-763G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786572 | |||||||
| chr7:102786580 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.932-755A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786580 | |||||||
| chr7:102786595 | A | G | 1 | a0004c0004t0001g0283 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.932-740A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786595 | |||||||
| chr7:102786606 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.932-729C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786606 | |||||||
| chr7:102786613 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.932-722G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786613 | |||||||
| chr7:102786841 | A | AAG | 126 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(123): Show |
147 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.932-494_932-493ins others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786841 | |||||||
| chr7:102786841 | A | AG | 78 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0028 others(75): Show |
91 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.932-494_932-493ins others(1): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786841 | |||||||
| chr7:102787021 | T | C | 131 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(128): Show |
153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-314T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787021 | |||||||
| chr7:102787041 | T | C | 2 | a0001c0001t0006g0045 a0001c0001t0006g0046 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.932-294T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787041 | |||||||
| chr7:102787111 | A | G | 4 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0212 others(1): Show |
5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-224A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787111 | |||||||
| chr7:102787209 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.932-126A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787209 | |||||||
| chr7:102787519 | A | G | 30 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(27): Show |
32 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1066+50A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787519 | |||||||
| chr7:102787729 | C | A | 1 | a0002c0002t0004g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1066+260C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787729 | |||||||
| chr7:102787983 | GAGAC | G | 4 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0212 others(1): Show |
5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+518_1066+521d others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102787983 | ||||||
| chr7:102787988 | A | T | 4 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0212 others(1): Show |
5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+519A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787988 | |||||||
| chr7:102787998 | T | A | 6 | a0001c0001t0001g0128 a0002c0002t0001g0218 a0002c0002t0001g0219 others(3): Show |
6 | HG01934.hp1 HG02071.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066+529T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787998 | |||||||
| chr7:102788050 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1066+581C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788050 | |||||||
| chr7:102788126 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1066+657G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788126 | |||||||
| chr7:102788365 | C | T | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+896C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788365 | |||||||
| chr7:102788657 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1066+1188G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788657 | |||||||
| chr7:102788681 | T | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
11 | HG02109.hp2 HG02572.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1066+1212T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788681 | |||||||
| chr7:102788811 | C | G | 2 | a0002c0002t0001g0207 a0002c0002t0004g0208 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+1342C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788811 | |||||||
| chr7:102788822 | G | T | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1066+1353G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788822 | |||||||
| chr7:102788841 | C | T | 206 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(203): Show |
240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1066+1372C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788841 | |||||||
| chr7:102788943 | T | TA | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+1475dupA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102788943 | ||||||
| chr7:102789008 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1066+1539G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789008 | |||||||
| chr7:102789168 | A | G | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+1699A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789168 | |||||||
| chr7:102789257 | T | C | 209 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(206): Show |
244 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.1066+1788T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789257 | |||||||
| chr7:102789272 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1066+1803G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789272 | |||||||
| chr7:102789274 | T | G | 210 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(207): Show |
245 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1066+1805T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789274 | |||||||
| chr7:102789276 | T | C | 209 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(206): Show |
244 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.1066+1807T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789276 | |||||||
| chr7:102789453 | A | C | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+1984A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789453 | |||||||
| chr7:102789566 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0204 a0001c0001t0001g0238 others(3): Show |
6 | HG02083.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066+2097G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789566 | |||||||
| chr7:102789570 | G | A | 1 | a0001c0001t0003g0120 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1066+2101G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789570 | |||||||
| chr7:102789704 | C | T | 31 | a0001c0001t0001g0113 a0001c0001t0001g0295 a0001c0001t0002g0007 others(28): Show |
38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1066+2235C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789704 | |||||||
| chr7:102789997 | G | A | 31 | a0001c0001t0001g0113 a0001c0001t0001g0295 a0001c0001t0002g0007 others(28): Show |
38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1066+2528G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789997 | |||||||
| chr7:102790020 | G | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0001t0001g0238 others(8): Show |
12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1066+2551G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790020 | |||||||
| chr7:102790075 | G | T | 124 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(121): Show |
146 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1066+2606G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790075 | |||||||
| chr7:102790316 | A | T | 2 | a0004c0004t0001g0278 a0004c0004t0001g0286 |
2 | HG00099.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1066+2847A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790316 | |||||||
| chr7:102790375 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1066+2906C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790375 | |||||||
| chr7:102790401 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0295 |
2 | NA18984.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1066+2932G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790401 | |||||||
| chr7:102791021 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1066+3552A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791021 | |||||||
| chr7:102791296 | AAAC | A | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1066+3831_1066+383 others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102791296 | ||||||
| chr7:102791318 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1066+3849G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791318 | |||||||
| chr7:102791729 | C | T | 50 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(47): Show |
61 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1066+4260C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791729 | |||||||
| chr7:102791892 | G | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1066+4423G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791892 | |||||||
| chr7:102792065 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(200): Show |
237 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1066+4596A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792065 | |||||||
| chr7:102792178 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1066+4709A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792178 | |||||||
| chr7:102792345 | T | C | 1 | a0001c0001t0003g0012 | 3 | NA18973.hp1 NA19010.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1066+4876T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792345 | |||||||
| chr7:102792556 | AG | A | 122 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(119): Show |
144 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1066+5089delG | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102792556 | ||||||
| chr7:102792631 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1066+5162A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792631 | |||||||
| chr7:102792643 | C | T | 3 | a0003c0003t0001g0078 a0003c0003t0001g0129 a0003c0003t0001g0139 |
3 | HG01106.hp2 HG01123.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1066+5174C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792643 | |||||||
| chr7:102792925 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG02896.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066+5456A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792925 | |||||||
| chr7:102792950 | G | A | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+5481G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792950 | |||||||
| chr7:102793057 | C | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1066+5588C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793057 | |||||||
| chr7:102793200 | GT | G | 194 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(191): Show |
228 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1066+5741delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102793200 | ||||||
| chr7:102793208 | T | G | 97 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(94): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1066+5739T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793208 | |||||||
| chr7:102793231 | A | G | 63 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0028 others(60): Show |
75 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1066+5762A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793231 | |||||||
| chr7:102793400 | C | T | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+5931C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793400 | |||||||
| chr7:102793414 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1066+5945A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793414 | |||||||
| chr7:102793488 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1066+6019C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793488 | |||||||
| chr7:102793715 | A | AT | 4 | a0001c0001t0002g0032 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
5 | NA18956.hp1 NA18979.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+6253dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102793715 | ||||||
| chr7:102793761 | G | A | 31 | a0001c0001t0001g0113 a0001c0001t0001g0295 a0001c0001t0002g0007 others(28): Show |
38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1066+6292G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793761 | |||||||
| chr7:102793771 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1066+6302G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793771 | |||||||
| chr7:102793952 | A | T | 29 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(26): Show |
31 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1066+6483A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793952 | |||||||
| chr7:102794035 | C | CA | 144 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(141): Show |
167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1066+6590dupA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102794035 | ||||||
| chr7:102794035 | C | CAA | 14 | a0001c0001t0001g0038 a0001c0001t0001g0082 a0001c0001t0001g0101 others(11): Show |
14 | HG00544.hp2 HG02148.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066+6589_1066+659 others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102794035 | ||||||
| chr7:102794035 | CA | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0083 a0001c0001t0001g0086 others(9): Show |
15 | HG00140.hp2 HG00323.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1066+6590delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102794035 | ||||||
| chr7:102794100 | C | T | 1 | a0004c0004t0001g0272 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1066+6631C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794100 | |||||||
| chr7:102794127 | A | C | 1 | a0001c0001t0002g0300 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1066+6658A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794127 | |||||||
| chr7:102794365 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0058 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1066+6896C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794365 | |||||||
| chr7:102794593 | T | A | 1 | a0003c0003t0001g0153 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1066+7124T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794593 | |||||||
| chr7:102794661 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1066+7192G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794661 | |||||||
| chr7:102794677 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG02896.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066+7208A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794677 | |||||||
| chr7:102794708 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1066+7239C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794708 | |||||||
| chr7:102794821 | C | T | 1 | a0003c0003t0001g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1066+7352C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794821 | |||||||
| chr7:102795001 | G | A | 123 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(120): Show |
145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1066+7532G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795001 | |||||||
| chr7:102795145 | A | G | 1 | a0001c0001t0002g0300 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1066+7676A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795145 | |||||||
| chr7:102795149 | G | A | 88 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0044 others(85): Show |
102 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1066+7680G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795149 | |||||||
| chr7:102795557 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1066+8088A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795557 | |||||||
| chr7:102795611 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0001g0245 |
3 | NA18942.hp1 NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1066+8142G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795611 | |||||||
| chr7:102795870 | T | C | 206 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(203): Show |
240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1066+8401T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795870 | |||||||
| chr7:102796243 | A | G | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+8774A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796243 | |||||||
| chr7:102796404 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1066+8935A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796404 | |||||||
| chr7:102796460 | G | A | 202 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(199): Show |
236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1066+8991G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796460 | |||||||
| chr7:102796818 | G | A | 201 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(198): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1066+9349G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796818 | |||||||
| chr7:102796888 | C | T | 1 | a0002c0002t0001g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1066+9419C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796888 | |||||||
| chr7:102797035 | T | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1066+9566T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797035 | |||||||
| chr7:102797134 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0060 others(11): Show |
18 | HG00621.hp2 HG01891.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.1066+9665G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797134 | |||||||
| chr7:102797448 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG02083.hp1 HG02132.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066+9979C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797448 | |||||||
| chr7:102797734 | A | G | 1 | a0001c0001t0004g0246 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1066+10265A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797734 | |||||||
| chr7:102798150 | A | G | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-10140A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798150 | |||||||
| chr7:102798187 | CAG | C | 3 | a0003c0003t0001g0140 a0003c0003t0001g0141 a0003c0003t0001g0147 |
3 | HG01258.hp2 HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1067-10102_1067-10 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798187 | |||||||
| chr7:102798212 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067-10078G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798212 | |||||||
| chr7:102798242 | C | A | 3 | a0003c0003t0001g0019 a0003c0003t0001g0063 a0003c0003t0001g0130 |
4 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-10048C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798242 | |||||||
| chr7:102798258 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1067-10032A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798258 | |||||||
| chr7:102798360 | A | G | 1 | a0003c0003t0001g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1067-9930A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798360 | |||||||
| chr7:102798415 | A | G | 1 | a0001c0001t0004g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1067-9875A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798415 | |||||||
| chr7:102798439 | T | C | 1 | a0002c0002t0001g0229 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1067-9851T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798439 | |||||||
| chr7:102798458 | G | T | 202 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(199): Show |
236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-9832G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798458 | |||||||
| chr7:102798459 | C | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(199): Show |
236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-9831C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798459 | |||||||
| chr7:102798500 | G | C | 127 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0043 others(124): Show |
149 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1067-9790G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798500 | |||||||
| chr7:102798667 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1067-9623G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798667 | |||||||
| chr7:102798784 | G | A | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-9506G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798784 | |||||||
| chr7:102798840 | T | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(202): Show |
239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1067-9450T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798840 | |||||||
| chr7:102798979 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-9311G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798979 | |||||||
| chr7:102799037 | C | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-9253C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799037 | |||||||
| chr7:102799100 | A | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(198): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1067-9190A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799100 | |||||||
| chr7:102799175 | G | T | 141 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(138): Show |
164 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1067-9115G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799175 | |||||||
| chr7:102799270 | G | A | 31 | a0001c0001t0001g0113 a0001c0001t0001g0295 a0001c0001t0002g0007 others(28): Show |
38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1067-9020G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799270 | |||||||
| chr7:102799409 | A | G | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-8881A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799409 | |||||||
| chr7:102799594 | G | A | 139 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(136): Show |
162 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1067-8696G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799594 | |||||||
| chr7:102799737 | T | C | 212 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(209): Show |
248 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1067-8553T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799737 | |||||||
| chr7:102800001 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1067-8289A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800001 | |||||||
| chr7:102800149 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1067-8141T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800149 | |||||||
| chr7:102800397 | T | C | 158 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(155): Show |
185 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1067-7893T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800397 | |||||||
| chr7:102800467 | C | T | 43 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(40): Show |
50 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1067-7823C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800467 | |||||||
| chr7:102800528 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1067-7762G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800528 | |||||||
| chr7:102800549 | A | G | 1 | a0002c0002t0004g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1067-7741A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800549 | |||||||
| chr7:102800644 | TA | T | 18 | a0001c0001t0001g0082 a0001c0001t0001g0105 a0001c0001t0001g0106 others(15): Show |
21 | HG00408.hp1 HG01934.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.1067-7644delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102800644 | ||||||
| chr7:102800653 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG02970.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1067-7637G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800653 | |||||||
| chr7:102800715 | C | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1067-7575C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800715 | |||||||
| chr7:102800733 | G | T | 210 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(207): Show |
247 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1067-7557G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800733 | |||||||
| chr7:102800923 | C | T | 1 | a0003c0003t0001g0140 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1067-7367C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800923 | |||||||
| chr7:102801089 | C | T | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1067-7201C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801089 | |||||||
| chr7:102801124 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1067-7166G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801124 | |||||||
| chr7:102801319 | T | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0009g0201 |
3 | HG01496.hp2 NA18975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1067-6971T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801319 | |||||||
| chr7:102801489 | G | T | 27 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(24): Show |
29 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1067-6801G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801489 | |||||||
| chr7:102801497 | C | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG03491.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1067-6793C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801497 | |||||||
| chr7:102801726 | G | A | 202 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(199): Show |
236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-6564G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801726 | |||||||
| chr7:102801743 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1067-6547G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801743 | |||||||
| chr7:102801785 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0178 |
2 | HG04199.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1067-6505C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801785 | |||||||
| chr7:102801818 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0004g0246 others(5): Show |
8 | HG02055.hp1 HG02486.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067-6472G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801818 | |||||||
| chr7:102801848 | G | C | 3 | a0003c0003t0001g0019 a0003c0003t0001g0063 a0003c0003t0001g0130 |
4 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-6442G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801848 | |||||||
| chr7:102801853 | C | G | 1 | a0001c0001t0003g0088 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1067-6437C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801853 | |||||||
| chr7:102801921 | CA | C | 173 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(170): Show |
206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.1067-6354delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102801921 | ||||||
| chr7:102801921 | CAA | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-6355_1067-635 others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102801921 | ||||||
| chr7:102802172 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG02896.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1067-6118A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802172 | |||||||
| chr7:102802177 | T | C | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-6113T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802177 | |||||||
| chr7:102802282 | A | G | 41 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0072 others(38): Show |
48 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1067-6008A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802282 | |||||||
| chr7:102802403 | C | A | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1067-5887C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802403 | |||||||
| chr7:102802499 | A | G | 1 | a0004c0004t0001g0274 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1067-5791A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802499 | |||||||
| chr7:102802721 | G | GAAAC | 143 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(140): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1067-5557_1067-555 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102802721 | ||||||
| chr7:102803026 | T | C | 1 | a0003c0003t0001g0147 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1067-5264T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803026 | |||||||
| chr7:102803045 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1067-5245T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803045 | |||||||
| chr7:102803093 | AC | A | 2 | a0003c0003t0001g0030 a0003c0003t0001g0258 |
3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1067-5195delC | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102803093 | ||||||
| chr7:102803141 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0004g0246 others(5): Show |
8 | HG02055.hp1 HG02486.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067-5149G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803141 | |||||||
| chr7:102803242 | A | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(140): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1067-5048A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803242 | |||||||
| chr7:102803248 | A | G | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-5042A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803248 | |||||||
| chr7:102803358 | G | C | 3 | a0003c0003t0001g0019 a0003c0003t0001g0063 a0003c0003t0001g0130 |
4 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-4932G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803358 | |||||||
| chr7:102803668 | A | G | 1 | a0001c0001t0004g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1067-4622A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803668 | |||||||
| chr7:102803706 | A | AAAGG | 201 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(198): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1067-4583_1067-458 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102803706 | ||||||
| chr7:102803726 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1067-4564A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803726 | |||||||
| chr7:102803777 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-4513A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803777 | |||||||
| chr7:102804078 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1067-4212G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804078 | |||||||
| chr7:102804095 | A | G | 140 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(137): Show |
166 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1067-4195A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804095 | |||||||
| chr7:102804285 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1067-4005C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804285 | |||||||
| chr7:102804376 | C | T | 26 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0101 others(23): Show |
28 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1067-3914C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804376 | |||||||
| chr7:102804536 | G | T | 3 | a0001c0001t0002g0289 a0001c0001t0002g0297 a0001c0001t0002g0298 |
3 | NA18971.hp1 NA19004.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1067-3754G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804536 | |||||||
| chr7:102804611 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1067-3679A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804611 | |||||||
| chr7:102804711 | T | C | 28 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0017 others(25): Show |
35 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1067-3579T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804711 | |||||||
| chr7:102805000 | G | T | 2 | a0003c0003t0001g0030 a0003c0003t0001g0258 |
3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1067-3290G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805000 | |||||||
| chr7:102805151 | A | G | 2 | a0001c0001t0006g0045 a0001c0001t0006g0046 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1067-3139A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805151 | |||||||
| chr7:102805324 | T | C | 1 | a0003c0003t0001g0126 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1067-2966T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805324 | |||||||
| chr7:102805345 | C | T | 1 | a0002c0002t0001g0213 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1067-2945C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805345 | |||||||
| chr7:102805381 | T | G | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-2909T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805381 | |||||||
| chr7:102805383 | A | G | 141 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(138): Show |
167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1067-2907A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805383 | |||||||
| chr7:102805424 | T | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-2866T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805424 | |||||||
| chr7:102805448 | T | C | 45 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0058 others(42): Show |
52 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1067-2842T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805448 | |||||||
| chr7:102805536 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1067-2754G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805536 | |||||||
| chr7:102805617 | C | T | 1 | a0001c0001t0005g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1067-2673C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805617 | |||||||
| chr7:102805677 | T | C | 28 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0017 others(25): Show |
35 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1067-2613T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805677 | |||||||
| chr7:102805725 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-2565G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805725 | |||||||
| chr7:102805732 | G | A | 2 | a0001c0001t0006g0045 a0001c0001t0006g0046 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1067-2558G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805732 | |||||||
| chr7:102805832 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1067-2458A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805832 | |||||||
| chr7:102806027 | G | C | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-2263G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806027 | |||||||
| chr7:102806122 | T | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(198): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1067-2168T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806122 | |||||||
| chr7:102806124 | ATTGTT | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0061 |
6 | HG00621.hp2 HG02027.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067-2163_1067-215 others(9): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806124 | ||||||
| chr7:102806142 | T | TTTG | 200 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(197): Show |
234 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1067-2130_1067-212 others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806142 | ||||||
| chr7:102806416 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(198): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1067-1874C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806416 | |||||||
| chr7:102806561 | G | GTTTT | 201 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(198): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1067-1728_1067-172 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806561 | ||||||
| chr7:102806577 | A | G | 1 | a0008c0007t0007g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1067-1713A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806577 | |||||||
| chr7:102806609 | T | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(198): Show |
235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1067-1681T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806609 | |||||||
| chr7:102806625 | TTC | T | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-1663_1067-166 others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806625 | ||||||
| chr7:102806643 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1067-1647G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806643 | |||||||
| chr7:102806692 | C | T | 2 | a0002c0002t0001g0224 a0002c0002t0001g0227 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1067-1598C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806692 | |||||||
| chr7:102806708 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067-1582T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806708 | |||||||
| chr7:102806719 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1067-1571C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806719 | |||||||
| chr7:102806884 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1067-1406C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806884 | |||||||
| chr7:102806894 | G | A | 78 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(75): Show |
93 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1067-1396G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806894 | |||||||
| chr7:102807025 | C | T | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-1265C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807025 | |||||||
| chr7:102807026 | A | G | 15 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(12): Show |
16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-1264A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807026 | |||||||
| chr7:102807069 | C | T | 1 | a0001c0001t0003g0118 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1067-1221C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807069 | |||||||
| chr7:102807170 | A | G | 3 | a0001c0001t0001g0048 a0002c0002t0001g0207 a0002c0002t0004g0208 |
3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-1120A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807170 | |||||||
| chr7:102807270 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1067-1020G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807270 | |||||||
| chr7:102807339 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1067-951A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807339 | |||||||
| chr7:102807544 | TC | T | 30 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0032 others(27): Show |
37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1067-745delC | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807544 | |||||||
| chr7:102807545 | C | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1067-745C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807545 | |||||||
| chr7:102807710 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1067-580G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807710 | |||||||
| chr7:102807744 | T | A | 2 | a0001c0001t0001g0048 a0002c0002t0001g0207 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1067-546T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807744 | |||||||
| chr7:102807750 | TAA | T | 108 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(105): Show |
132 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1067-524_1067-523d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102807750 | ||||||
| chr7:102807750 | TAAA | T | 28 | a0001c0001t0001g0047 a0001c0001t0001g0079 a0001c0001t0001g0080 others(25): Show |
30 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1067-525_1067-523d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102807750 | ||||||
| chr7:102807751 | A | T | 33 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0001g0134 others(30): Show |
40 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1067-539A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807751 | |||||||
| chr7:102807781 | GGGCGTGG others(25): Show |
G | 1 | a0001c0001t0003g0107 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1067-508_1067-477d others(34): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807781 | |||||||
| chr7:102807830 | G | T | 4 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0212 others(1): Show |
5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067-460G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807830 | |||||||
| chr7:102807932 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1067-358G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807932 | |||||||
| chr7:102808008 | C | T | 31 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0001g0134 others(28): Show |
38 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1067-282C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102808008 | |||||||
| chr7:102808024 | G | C | 1 | a0002c0002t0001g0207 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1067-266G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102808024 | |||||||
| chr7:102808217 | C | T | 142 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(139): Show |
168 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1067-73C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102808217 |