Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51495 |
| ensemblid | ENSG00000074696.13 |
| hgncid | 24175 |
| symbol | HACD3 |
| name | 3-hydroxyacyl-CoA dehydratase 3 |
| refseq_nuc | NM_016395.4 |
| refseq_prot | NP_057479.2 |
| ensembl_nuc | ENST00000261875.10 |
| ensembl_prot | ENSP00000261875.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 65530463 |
| end | 65578349 |
| strand | + |
| ver | v1.2 |
| region | chr15:65530463-65578349 |
| region5000 | chr15:65525463-65583349 |
| regionname0 | HACD3_chr15_65530463_65578349 |
| regionname5000 | HACD3_chr15_65525463_65583349 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 362 | 303 | 87 | 47 | 117 | 12 | 38 | 90 | HACD3_chr15_65525463_65583349 | HACD3 | MENQV others(357): Show |
chr15 | 65525463 | 65583349 |
| a0002 | 0/0 | 362 | 23 | 7 | 5 | 7 | 0 | 4 | 4 | HACD3_chr15_65525463_65583349 | HACD3 | MENQV others(357): Show |
chr15 | 65525463 | 65583349 |
| a0003 | 0/0 | 362 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | MENQV others(357): Show |
chr15 | 65525463 | 65583349 |
| a0004 | 0/0 | 362 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | MENQV others(357): Show |
chr15 | 65525463 | 65583349 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1086 | 280 | 87 | 37 | 109 | 11 | 34 | HACD3_chr15_65525463_65583349 | HACD3 | ATGGA others(1081): Show |
chr15 | 65525463 | 65583349 | ||
| a0001c0002 | 0/0 | 1086 | 23 | 0 | 10 | 8 | 1 | 4 | HACD3_chr15_65525463_65583349 | HACD3 | ATGGA others(1081): Show |
chr15 | 65525463 | 65583349 | ||
| a0002c0003 | 0/0 | 1086 | 23 | 7 | 5 | 7 | 0 | 4 | HACD3_chr15_65525463_65583349 | HACD3 | ATGGA others(1081): Show |
chr15 | 65525463 | 65583349 | ||
| a0003c0004 | 0/0 | 1086 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | ATGGA others(1081): Show |
chr15 | 65525463 | 65583349 | ||
| a0004c0005 | 0/0 | 1086 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | ATGGA others(1081): Show |
chr15 | 65525463 | 65583349 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3228 | 191 | 25 | 32 | 100 | 7 | 26 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0002 | 0/0 | 3228 | 45 | 34 | 3 | 0 | 4 | 4 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0004 | 0/0 | 3231 | 9 | 9 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3226): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0005 | 0/0 | 3233 | 7 | 5 | 2 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3228): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0006 | 0/0 | 3228 | 7 | 7 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0007 | 0/0 | 3228 | 5 | 1 | 0 | 4 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0008 | 0/0 | 3228 | 3 | 0 | 0 | 3 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0009 | 0/0 | 3228 | 3 | 2 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0010 | 0/0 | 3228 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0011 | 0/0 | 3228 | 2 | 0 | 0 | 0 | 0 | 2 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0012 | 0/0 | 3228 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0014 | 1/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0015 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0016 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0001t0017 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0002t0002 | 0/0 | 3228 | 21 | 0 | 10 | 7 | 1 | 3 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0002t0018 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0001c0002t0020 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0002c0003t0003 | 0/0 | 3228 | 22 | 6 | 5 | 7 | 0 | 4 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0002c0003t0013 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0003c0004t0019 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| a0004c0005t0002 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | GTCAC others(3223): Show |
chr15 | 65525463 | 65583349 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 1 | 5 | 2 | 1 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0002 | 0/0 | 9 | 1 | 0 | 7 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0011g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0014g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0015g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0016g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0001t0017g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0018g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0001c0002t0020g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0002c0003t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0003c0004t0019g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| a0004c0005t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0025 | EUR | FIN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00423 | hp2 | a0001 | c0001 | t0017 | g0118 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0170 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00642 | hp2 | a0002 | c0003 | t0003 | g0240 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00673 | hp1 | a0002 | c0003 | t0003 | g0032 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0239 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01069 | hp1 | a0002 | c0003 | t0003 | g0246 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0186 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01109 | hp2 | a0003 | c0004 | t0019 | g0038 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0257 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01168 | hp1 | a0002 | c0003 | t0003 | g0241 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0261 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0242 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0212 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | IBS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | IBS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0029 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0229 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02040 | hp2 | a0001 | c0002 | t0020 | g0220 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0171 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02080 | hp2 | a0002 | c0003 | t0003 | g0032 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0268 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02300 | hp2 | a0004 | c0005 | t0002 | g0003 | AMR | PEL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0254 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02647 | hp2 | a0002 | c0003 | t0003 | g0234 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02683 | hp1 | a0002 | c0003 | t0003 | g0232 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02698 | hp1 | a0001 | c0001 | t0015 | g0160 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0040 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0247 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02965 | hp1 | a0002 | c0003 | t0003 | g0245 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0269 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0243 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0263 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0238 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0034 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0222 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0214 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0207 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0089 | AFR | ESN | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0253 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03669 | hp2 | a0002 | c0003 | t0003 | g0227 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0210 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03710 | hp2 | a0002 | c0003 | t0003 | g0226 | SAS | PJL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0158 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0159 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03927 | hp1 | a0001 | c0002 | t0018 | g0029 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04204 | hp2 | a0002 | c0003 | t0003 | g0233 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | STU | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | YRI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | YRI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18947 | hp1 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18972 | hp1 | a0002 | c0003 | t0003 | g0228 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18984 | hp1 | a0001 | c0001 | t0016 | g0100 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18986 | hp1 | a0001 | c0001 | t0007 | g0172 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18992 | hp1 | a0002 | c0003 | t0003 | g0230 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19006 | hp1 | a0002 | c0003 | t0003 | g0225 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0231 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | LWK | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | LWK | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0236 | AFR | LWK | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0055 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | YRI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ASW | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0197 | EUR | TSI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02109 | hp2 | a0002 | c0003 | t0013 | g0237 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02486 | hp1 | a0002 | c0003 | t0003 | g0235 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0252 | AFR | MSL | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | USA | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0251 | AFR | USA | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0164 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | USA | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | USA | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | LWK | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0061 | REF | REF | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0244 | REF | REF | HACD3_chr15_65525463_65583349 | HACD3 | chr15 | 65525463 | 65583349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:65554940 | T | G | 1 | a0003 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.184T>G | p.Leu62Val | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/11 | 353/3228 | 184/1089 | 62/362 | chr15 | 65554940 | |||
| chr15:65558702 | T | A | 1 | a0004 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.392T>A | p.Leu131His | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/11 | 561/3228 | 392/1089 | 131/362 | chr15 | 65558702 | |||
| chr15:65571579 | A | C | 1 | a0002 | 23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
missense_variant | MODERATE | c.805A>C | p.Met269Leu | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 9/11 | 974/3228 | 805/1089 | 269/362 | chr15 | 65571579 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:65564315 | G | A | 3 | a0001c0002 a0002c0003 a0004c0005 |
47 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(44): Show |
synonymous_variant | LOW | c.633G>A | p.Thr211Thr | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/11 | 802/3228 | 633/1089 | 211/362 | chr15 | 65564315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:65530485 | C | G | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(13): Show |
285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
5_prime_UTR_variant | MODIFIER | c.-147C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/11 | 147 | chr15 | 65530485 | ||||||
| chr15:65530495 | G | T | 1 | a0001c0002t0020 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/11 | 137 | chr15 | 65530495 | ||||||
| chr15:65576509 | T | C | 1 | a0002c0003t0013 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 130 | chr15 | 65576509 | ||||||
| chr15:65576643 | A | C | 2 | a0002c0003t0003 a0002c0003t0013 |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*264A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 264 | chr15 | 65576643 | ||||||
| chr15:65576707 | C | A | 2 | a0001c0001t0011 a0001c0001t0015 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*328C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 328 | chr15 | 65576707 | ||||||
| chr15:65576727 | C | G | 1 | a0001c0001t0009 | 3 | HG02647.hp1 HG03239.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*348C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 348 | chr15 | 65576727 | ||||||
| chr15:65576934 | C | T | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(11): Show |
123 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*555C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 555 | chr15 | 65576934 | ||||||
| chr15:65576981 | C | T | 1 | a0001c0001t0008 | 3 | NA18947.hp1 NA18955.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*602C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 602 | chr15 | 65576981 | ||||||
| chr15:65577107 | T | C | 1 | a0001c0002t0018 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*728T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 728 | chr15 | 65577107 | ||||||
| chr15:65577284 | G | T | 1 | a0001c0001t0017 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*905G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 905 | chr15 | 65577284 | ||||||
| chr15:65577372 | C | T | 1 | a0003c0004t0019 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 993 | chr15 | 65577372 | ||||||
| chr15:65577458 | T | TACAC | 1 | a0001c0001t0004 | 9 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1092_*1095dupACAC | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1096 | INFO_REALIGN_3_PRIME | chr15 | 65577458 | |||||
| chr15:65577458 | T | TACACAC | 1 | a0001c0001t0005 | 7 | HG01167.hp1 HG01169.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1090_*1095dupACAC others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1096 | INFO_REALIGN_3_PRIME | chr15 | 65577458 | |||||
| chr15:65577575 | G | A | 1 | a0001c0001t0016 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1196G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1196 | chr15 | 65577575 | ||||||
| chr15:65577676 | AG | A | 2 | a0001c0001t0004 a0001c0001t0005 |
16 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1298delG | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1298 | chr15 | 65577676 | ||||||
| chr15:65577744 | G | C | 1 | a0001c0001t0009 | 3 | HG02647.hp1 HG03239.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1365G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1365 | chr15 | 65577744 | ||||||
| chr15:65577792 | G | A | 6 | a0001c0001t0002 a0001c0001t0012 a0001c0002t0002 others(3): Show |
71 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1413G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1413 | chr15 | 65577792 | ||||||
| chr15:65577971 | G | C | 1 | a0001c0001t0015 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1592 | chr15 | 65577971 | ||||||
| chr15:65578037 | C | G | 1 | a0001c0001t0012 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1658C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1658 | chr15 | 65578037 | ||||||
| chr15:65578116 | T | C | 1 | a0001c0001t0007 | 5 | HG00621.hp2 HG02056.hp2 HG03516.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1737T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1737 | chr15 | 65578116 | ||||||
| chr15:65578170 | G | A | 1 | a0001c0001t0015 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1791 | chr15 | 65578170 | ||||||
| chr15:65578285 | C | G | 1 | a0003c0004t0019 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1906C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 11/11 | 1906 | chr15 | 65578285 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:65530870 | T | G | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.87+152T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65530870 | |||||||
| chr15:65530940 | C | G | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.87+222C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65530940 | |||||||
| chr15:65531036 | T | C | 3 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0037 |
3 | HG03130.hp1 HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.87+318T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531036 | |||||||
| chr15:65531224 | T | TGGGGGAG others(10): Show |
1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.87+511_87+512insAG others(15): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65531224 | ||||||
| chr15:65531445 | C | G | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.87+727C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531445 | |||||||
| chr15:65531500 | G | A | 1 | a0001c0001t0004g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.87+782G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531500 | |||||||
| chr15:65531541 | T | C | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.87+823T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531541 | |||||||
| chr15:65531552 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.87+834T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531552 | |||||||
| chr15:65531555 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.87+837C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531555 | |||||||
| chr15:65531559 | CT | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
265 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.87+850delT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65531559 | ||||||
| chr15:65531563 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0042 others(4): Show |
9 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.87+845T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531563 | |||||||
| chr15:65531583 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.87+865G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531583 | |||||||
| chr15:65531653 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.87+935C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531653 | |||||||
| chr15:65531690 | C | T | 3 | a0001c0001t0009g0034 a0001c0001t0009g0043 a0001c0001t0009g0044 |
3 | HG02647.hp1 HG03239.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.87+972C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531690 | |||||||
| chr15:65531766 | A | T | 1 | a0001c0002t0002g0223 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.87+1048A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531766 | |||||||
| chr15:65531773 | C | T | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.87+1055C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65531773 | |||||||
| chr15:65532111 | A | G | 57 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(54): Show |
69 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.87+1393A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532111 | |||||||
| chr15:65532236 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.87+1518C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532236 | |||||||
| chr15:65532281 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+1563A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532281 | |||||||
| chr15:65532525 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.87+1807G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532525 | |||||||
| chr15:65532563 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.87+1845C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532563 | |||||||
| chr15:65532637 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.87+1919A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532637 | |||||||
| chr15:65532710 | G | C | 1 | a0001c0001t0002g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.87+1992G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532710 | |||||||
| chr15:65532857 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.87+2139G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532857 | |||||||
| chr15:65532917 | CAA | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.87+2203_87+2204del others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65532917 | ||||||
| chr15:65532936 | G | A | 1 | a0001c0001t0006g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.87+2218G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532936 | |||||||
| chr15:65532973 | C | T | 1 | a0001c0002t0020g0220 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.87+2255C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65532973 | |||||||
| chr15:65533136 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+2418A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533136 | |||||||
| chr15:65533215 | A | G | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG02630.hp2 HG02723.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+2497A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533215 | |||||||
| chr15:65533353 | C | T | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.87+2635C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533353 | |||||||
| chr15:65533388 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.87+2670G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533388 | |||||||
| chr15:65533454 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+2736A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533454 | |||||||
| chr15:65533744 | T | TA | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(215): Show |
270 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.87+3040dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65533744 | ||||||
| chr15:65533774 | G | A | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.87+3056G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533774 | |||||||
| chr15:65533792 | C | G | 1 | a0001c0001t0004g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.87+3074C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533792 | |||||||
| chr15:65533808 | A | G | 4 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG03688.hp2 HG03704.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+3090A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533808 | |||||||
| chr15:65533848 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG01123.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.87+3130G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533848 | |||||||
| chr15:65533968 | G | A | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+3250G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65533968 | |||||||
| chr15:65534047 | T | C | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.87+3329T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65534047 | |||||||
| chr15:65534050 | C | CA | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+3347dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65534050 | ||||||
| chr15:65534050 | CA | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(236): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.87+3347delA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65534050 | ||||||
| chr15:65534061 | A | G | 2 | a0001c0001t0010g0268 a0001c0001t0010g0269 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.87+3343A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65534061 | |||||||
| chr15:65534338 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+3620G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65534338 | |||||||
| chr15:65534422 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01433.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.87+3704G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65534422 | |||||||
| chr15:65534501 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.87+3783A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65534501 | |||||||
| chr15:65534645 | T | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+3927T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65534645 | |||||||
| chr15:65534892 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.87+4174C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65534892 | |||||||
| chr15:65535018 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+4300G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535018 | |||||||
| chr15:65535025 | C | T | 4 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0171 others(1): Show |
4 | HG00621.hp2 HG02056.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+4307C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535025 | |||||||
| chr15:65535136 | C | T | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.87+4418C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535136 | |||||||
| chr15:65535138 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.87+4420C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535138 | |||||||
| chr15:65535237 | A | G | 1 | a0001c0001t0009g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.87+4519A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535237 | |||||||
| chr15:65535238 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.87+4520A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535238 | |||||||
| chr15:65535321 | T | C | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.87+4603T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535321 | |||||||
| chr15:65535523 | C | T | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | NA18947.hp1 NA18949.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+4805C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535523 | |||||||
| chr15:65535534 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.87+4816A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535534 | |||||||
| chr15:65535652 | A | T | 1 | a0001c0001t0002g0031 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.87+4934A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65535652 | |||||||
| chr15:65536003 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+5285T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536003 | |||||||
| chr15:65536019 | T | G | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+5301T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536019 | |||||||
| chr15:65536055 | C | G | 1 | a0001c0001t0002g0030 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.87+5337C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536055 | |||||||
| chr15:65536161 | C | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
6 | NA18612.hp1 NA18950.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+5443C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536161 | |||||||
| chr15:65536315 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.87+5597A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536315 | |||||||
| chr15:65536350 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.87+5632A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536350 | |||||||
| chr15:65536441 | C | G | 2 | a0001c0001t0010g0268 a0001c0001t0010g0269 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.87+5723C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536441 | |||||||
| chr15:65536476 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG02071.hp2 NA18942.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+5758T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536476 | |||||||
| chr15:65536713 | G | A | 1 | a0002c0003t0013g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.87+5995G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65536713 | |||||||
| chr15:65537054 | A | G | 3 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0015g0160 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.87+6336A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537054 | |||||||
| chr15:65537377 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.87+6659G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537377 | |||||||
| chr15:65537462 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0156 |
3 | HG01884.hp1 HG02300.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.87+6744C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537462 | |||||||
| chr15:65537525 | T | G | 2 | a0001c0002t0002g0185 a0001c0002t0002g0186 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.87+6807T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537525 | |||||||
| chr15:65537529 | G | A | 1 | a0001c0001t0006g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.87+6811G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537529 | |||||||
| chr15:65537665 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | NA18983.hp1 NA19006.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+6947C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537665 | |||||||
| chr15:65537707 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.87+6989C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537707 | |||||||
| chr15:65537783 | ACT | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.87+7068_87+7069del others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537783 | ||||||
| chr15:65537792 | C | CAAAAAA | 15 | a0001c0001t0001g0049 a0001c0001t0001g0062 a0001c0001t0002g0181 others(12): Show |
15 | HG00621.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.87+7086_87+7091dup others(6): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537792 | ||||||
| chr15:65537792 | C | CAAAAAAA others(1): Show |
23 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0046 others(20): Show |
24 | HG00140.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.87+7084_87+7091dup others(8): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537792 | ||||||
| chr15:65537792 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.87+7081_87+7091dup others(11): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537792 | ||||||
| chr15:65537943 | AAAAAAAA others(14): Show |
A | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.87+7227_87+7247del others(21): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537943 | ||||||
| chr15:65537945 | AAAAAAAA others(14): Show |
A | 2 | a0001c0001t0001g0105 a0001c0001t0002g0221 |
2 | HG02717.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.87+7229_87+7249del others(21): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537945 | ||||||
| chr15:65537945 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0004g0267 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.87+7229_87+7257del others(29): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537945 | ||||||
| chr15:65537946 | AAAAAAAA others(17): Show |
A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0006g0222 others(1): Show |
4 | HG01099.hp2 HG02280.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+7230_87+7253del others(24): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537946 | ||||||
| chr15:65537946 | AAAAAAAA others(19): Show |
A | 3 | a0001c0001t0004g0036 a0001c0001t0005g0257 a0001c0001t0005g0261 |
3 | HG01167.hp1 HG01169.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.87+7230_87+7255del others(26): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537946 | ||||||
| chr15:65537946 | AAAAAAAA others(21): Show |
A | 2 | a0001c0001t0001g0009 a0001c0001t0004g0037 |
2 | HG00609.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.87+7230_87+7257del others(28): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537946 | ||||||
| chr15:65537946 | AAAAAAAA others(25): Show |
A | 1 | a0001c0001t0004g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.87+7230_87+7261del others(32): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537946 | ||||||
| chr15:65537947 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0006g0253 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.87+7231_87+7247del others(17): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537947 | ||||||
| chr15:65537947 | AAAAAAAA others(14): Show |
A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0078 |
2 | HG04184.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.87+7231_87+7251del others(21): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537947 | ||||||
| chr15:65537947 | AAAAAAAA others(16): Show |
A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0131 |
3 | NA18995.hp1 NA18995.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.87+7231_87+7253del others(23): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537947 | ||||||
| chr15:65537947 | AAAAAAAA others(18): Show |
A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0096 a0001c0001t0001g0101 others(5): Show |
8 | HG00735.hp1 HG01109.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.87+7231_87+7255del others(25): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537947 | ||||||
| chr15:65537947 | AAAAAAAA others(20): Show |
A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0151 a0001c0001t0001g0224 others(3): Show |
6 | HG01433.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+7231_87+7257del others(27): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537947 | ||||||
| chr15:65537947 | AAAAAAAA others(22): Show |
A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0125 a0001c0001t0004g0033 |
4 | HG02622.hp1 HG03041.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+7231_87+7259del others(29): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537947 | ||||||
| chr15:65537948 | AAAAAAAA others(15): Show |
A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0056 others(5): Show |
8 | HG01433.hp1 HG02602.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.87+7232_87+7253del others(22): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537948 | ||||||
| chr15:65537948 | AAAAAAAA others(17): Show |
A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(15): Show |
20 | HG00140.hp2 HG00544.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.87+7232_87+7255del others(24): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537948 | ||||||
| chr15:65537948 | AAAAAAAA others(19): Show |
A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0098 others(9): Show |
13 | HG02080.hp1 HG02896.hp1 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.87+7232_87+7257del others(26): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537948 | ||||||
| chr15:65537948 | AAAAAAAA others(21): Show |
A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0102 others(4): Show |
7 | HG00544.hp1 HG00621.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+7232_87+7259del others(28): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537948 | ||||||
| chr15:65537949 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0007g0171 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.87+7233_87+7245del others(13): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537949 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0006g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.87+7233_87+7247del others(15): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537949 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0006g0251 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.87+7233_87+7249del others(17): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537949 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0006g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.87+7233_87+7251del others(19): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537949 | AAAAAAAA others(14): Show |
A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0093 |
2 | NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.87+7233_87+7253del others(21): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537949 | AAAAAAAA others(16): Show |
A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0070 others(7): Show |
12 | HG01123.hp1 HG02886.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.87+7233_87+7255del others(23): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537949 | AAAAAAAA others(18): Show |
A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(8): Show |
11 | HG00408.hp1 HG02004.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.87+7233_87+7257del others(25): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537949 | AAAAAAAA others(20): Show |
A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(38): Show |
49 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.87+7233_87+7259del others(27): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537949 | ||||||
| chr15:65537950 | AAAAAAAA others(5): Show |
A | 1 | a0002c0003t0003g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.87+7234_87+7245del others(12): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537950 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0007g0172 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.87+7234_87+7247del others(14): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537950 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0007g0169 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.87+7234_87+7249del others(16): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537950 | AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0086 |
2 | HG04199.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.87+7234_87+7253del others(20): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537950 | AAAAAAAA others(15): Show |
A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0138 others(4): Show |
7 | HG01070.hp2 HG01346.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.87+7234_87+7255del others(22): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537950 | AAAAAAAA others(17): Show |
A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(19): Show |
26 | HG00323.hp1 HG00423.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.87+7234_87+7257del others(24): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537950 | AAAAAAAA others(19): Show |
A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0001t0002g0004 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+7234_87+7259del others(26): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537950 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.87+7234_87+7261del others(28): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537950 | ||||||
| chr15:65537951 | AAAAAAAA others(8): Show |
A | 1 | a0001c0002t0002g0184 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.87+7235_87+7249del others(15): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537951 | ||||||
| chr15:65537951 | AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0006g0254 a0001c0001t0007g0170 |
2 | HG00621.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.87+7235_87+7251del others(17): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537951 | ||||||
| chr15:65537951 | AAAAAAAA others(16): Show |
A | 3 | a0001c0001t0001g0124 a0001c0001t0002g0028 a0001c0001t0002g0200 |
4 | HG02451.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+7235_87+7257del others(23): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537951 | ||||||
| chr15:65537951 | AAAAAAAA others(18): Show |
A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0103 a0001c0001t0002g0004 others(4): Show |
7 | HG00323.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.87+7235_87+7259del others(25): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537951 | ||||||
| chr15:65537951 | AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0001g0010 a0001c0001t0017g0118 |
2 | HG00423.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.87+7235_87+7261del others(27): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537951 | ||||||
| chr15:65537951 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.87+7235_87+7263del others(29): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537951 | ||||||
| chr15:65537952 | A | T | 1 | a0001c0001t0007g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.87+7234A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537952 | |||||||
| chr15:65537952 | AAAAAAAA others(13): Show |
A | 5 | a0001c0002t0002g0003 a0001c0002t0002g0191 a0001c0002t0002g0192 others(2): Show |
8 | HG02273.hp1 HG02293.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.87+7236_87+7255del others(20): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537952 | ||||||
| chr15:65537952 | AAAAAAAA others(15): Show |
A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0088 others(2): Show |
8 | HG00733.hp2 HG01952.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.87+7236_87+7257del others(22): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537952 | ||||||
| chr15:65537952 | AAAAAAAA others(17): Show |
A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0050 others(11): Show |
14 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.87+7236_87+7259del others(24): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537952 | ||||||
| chr15:65537952 | AAAAAAAA others(19): Show |
A | 8 | a0001c0001t0002g0004 a0001c0001t0002g0027 a0001c0001t0002g0031 others(5): Show |
8 | HG00140.hp1 HG01517.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.87+7236_87+7261del others(26): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537952 | ||||||
| chr15:65537952 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0143 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.87+7236_87+7263del others(28): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537952 | ||||||
| chr15:65537953 | AAAAAAAT others(12): Show |
A | 2 | a0001c0001t0006g0247 a0001c0001t0009g0034 |
2 | HG02922.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.87+7237_87+7255del others(19): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537953 | ||||||
| chr15:65537953 | AAAAAAAT others(14): Show |
A | 1 | a0001c0002t0002g0004 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.87+7237_87+7257del others(21): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537953 | ||||||
| chr15:65537953 | AAAAAAAT others(18): Show |
A | 19 | a0001c0001t0002g0024 a0001c0001t0002g0026 a0001c0001t0002g0027 others(16): Show |
20 | HG01515.hp1 HG01934.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.87+7237_87+7261del others(25): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537953 | ||||||
| chr15:65537953 | AAAAAAAT others(20): Show |
A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0271 |
2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.87+7237_87+7263del others(27): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537953 | ||||||
| chr15:65537954 | A | T | 1 | a0001c0001t0007g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.87+7236A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537954 | |||||||
| chr15:65537954 | AAAAAATA others(15): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.87+7238_87+7259del others(22): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537954 | ||||||
| chr15:65537954 | AAAAAATA others(17): Show |
A | 6 | a0001c0001t0001g0048 a0001c0001t0002g0030 a0001c0001t0011g0159 others(3): Show |
6 | HG01346.hp1 HG01884.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+7238_87+7261del others(24): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537954 | ||||||
| chr15:65537954 | AAAAAATA others(19): Show |
A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0270 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.87+7238_87+7263del others(26): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537954 | ||||||
| chr15:65537955 | AAAAATAT others(8): Show |
A | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.87+7239_87+7253del others(15): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537955 | ||||||
| chr15:65537955 | AAAAATAT others(18): Show |
A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0190 a0001c0001t0002g0196 others(1): Show |
4 | HG01993.hp1 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+7239_87+7263del others(25): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537955 | ||||||
| chr15:65537956 | A | T | 1 | a0001c0001t0007g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.87+7238A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537956 | |||||||
| chr15:65537958 | A | T | 1 | a0001c0001t0007g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.87+7240A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537958 | |||||||
| chr15:65537958 | AATATATA others(3): Show |
A | 3 | a0002c0003t0003g0032 a0002c0003t0003g0232 a0002c0003t0003g0233 |
3 | HG02080.hp2 HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.87+7273_87+7282del others(10): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65537958 | ||||||
| chr15:65537959 | ATATATAT others(2): Show |
A | 6 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0228 others(3): Show |
6 | HG00673.hp1 HG02027.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+7242_87+7250del others(9): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537959 | |||||||
| chr15:65537962 | T | A | 1 | a0002c0003t0013g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.87+7244T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537962 | |||||||
| chr15:65537964 | T | A | 3 | a0002c0003t0003g0238 a0002c0003t0003g0243 a0002c0003t0003g0245 |
3 | HG02965.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.87+7246T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537964 | |||||||
| chr15:65537966 | T | A | 1 | a0002c0003t0003g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.87+7248T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537966 | |||||||
| chr15:65537968 | T | A | 2 | a0002c0003t0003g0226 a0002c0003t0003g0227 |
2 | HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.87+7250T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537968 | |||||||
| chr15:65537970 | T | A | 9 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(6): Show |
10 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.87+7252T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537970 | |||||||
| chr15:65537972 | T | A | 7 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0228 others(4): Show |
8 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.87+7254T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537972 | |||||||
| chr15:65537974 | T | A | 5 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0228 others(2): Show |
6 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+7256T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65537974 | |||||||
| chr15:65538049 | C | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG02071.hp2 NA18942.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+7331C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538049 | |||||||
| chr15:65538168 | GA | G | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+7454delA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65538168 | ||||||
| chr15:65538180 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(162): Show |
205 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.87+7462C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538180 | |||||||
| chr15:65538181 | G | A | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.87+7463G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538181 | |||||||
| chr15:65538192 | A | ACTGT | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+7476_87+7479dup others(4): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65538192 | ||||||
| chr15:65538211 | C | A | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+7493C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538211 | |||||||
| chr15:65538244 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+7526T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538244 | |||||||
| chr15:65538530 | G | C | 6 | a0001c0002t0002g0003 a0001c0002t0002g0184 a0001c0002t0002g0191 others(3): Show |
9 | HG02273.hp1 HG02293.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.87+7812G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538530 | |||||||
| chr15:65538538 | G | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG00738.hp2 HG01243.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+7820G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538538 | |||||||
| chr15:65538681 | G | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01099.hp2 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.87+7963G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538681 | |||||||
| chr15:65538806 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.87+8088G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538806 | |||||||
| chr15:65538839 | A | T | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.87+8121A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538839 | |||||||
| chr15:65538937 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.87+8219G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65538937 | |||||||
| chr15:65539012 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.87+8294A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539012 | |||||||
| chr15:65539187 | T | A | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.87+8469T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539187 | |||||||
| chr15:65539210 | CTT | C | 11 | a0001c0001t0001g0045 a0001c0001t0001g0146 a0001c0001t0001g0147 others(8): Show |
11 | HG00609.hp1 HG00673.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+8518_87+8519del others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65539210 | ||||||
| chr15:65539210 | CTTT | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.87+8517_87+8519del others(3): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65539210 | ||||||
| chr15:65539210 | CTTTT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(127): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.87+8516_87+8519del others(4): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65539210 | ||||||
| chr15:65539259 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+8541A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539259 | |||||||
| chr15:65539301 | A | G | 1 | a0001c0001t0009g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.87+8583A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539301 | |||||||
| chr15:65539362 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+8644G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539362 | |||||||
| chr15:65539510 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.87+8792C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539510 | |||||||
| chr15:65539631 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.87+8913T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539631 | |||||||
| chr15:65539753 | A | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0249 |
3 | HG02080.hp1 NA19010.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.87+9035A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539753 | |||||||
| chr15:65539829 | CAAAT | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
276 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.87+9115_87+9118del others(4): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65539829 | ||||||
| chr15:65539951 | C | T | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.87+9233C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539951 | |||||||
| chr15:65539953 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.87+9235A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539953 | |||||||
| chr15:65539982 | C | T | 2 | a0001c0001t0006g0222 a0003c0004t0019g0038 |
2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.87+9264C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65539982 | |||||||
| chr15:65540149 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.87+9431T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540149 | |||||||
| chr15:65540223 | T | A | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.87+9505T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540223 | |||||||
| chr15:65540308 | A | G | 1 | a0001c0001t0010g0269 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.87+9590A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540308 | |||||||
| chr15:65540514 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.87+9796G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540514 | |||||||
| chr15:65540653 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.87+9935A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540653 | |||||||
| chr15:65540837 | C | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.87+10119C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540837 | |||||||
| chr15:65540972 | C | T | 2 | a0001c0001t0010g0268 a0001c0001t0010g0269 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.87+10254C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540972 | |||||||
| chr15:65540994 | A | T | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.87+10276A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65540994 | |||||||
| chr15:65541177 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG00140.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.87+10459C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541177 | |||||||
| chr15:65541622 | T | C | 4 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0194 others(1): Show |
4 | HG02615.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-10054T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541622 | |||||||
| chr15:65541693 | T | G | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-9983T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541693 | |||||||
| chr15:65541762 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.88-9914G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541762 | |||||||
| chr15:65541840 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(217): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.88-9836A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541840 | |||||||
| chr15:65541945 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01099.hp2 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.88-9731T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541945 | |||||||
| chr15:65541960 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0012g0040 a0001c0001t0012g0041 |
4 | HG02615.hp2 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-9716G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541960 | |||||||
| chr15:65541966 | C | T | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-9710C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65541966 | |||||||
| chr15:65542097 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-9579C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542097 | |||||||
| chr15:65542227 | C | CA | 18 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0099 others(15): Show |
19 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.88-9430dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65542227 | ||||||
| chr15:65542227 | C | CAA | 73 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(70): Show |
86 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.88-9431_88-9430dup others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65542227 | ||||||
| chr15:65542227 | CA | C | 8 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0140 others(5): Show |
8 | HG01069.hp1 HG01167.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-9430delA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65542227 | ||||||
| chr15:65542243 | AAAAG | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
95 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.88-9429_88-9426del others(4): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65542243 | ||||||
| chr15:65542378 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.88-9298C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542378 | |||||||
| chr15:65542512 | C | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0177 |
2 | HG00735.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.88-9164C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542512 | |||||||
| chr15:65542649 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-9027G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542649 | |||||||
| chr15:65542654 | C | T | 1 | a0001c0002t0002g0193 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.88-9022C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542654 | |||||||
| chr15:65542743 | A | G | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-8933A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542743 | |||||||
| chr15:65542871 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-8805A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542871 | |||||||
| chr15:65542892 | G | T | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG02630.hp2 HG02723.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.88-8784G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542892 | |||||||
| chr15:65542947 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.88-8729G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542947 | |||||||
| chr15:65542998 | C | T | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-8678C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65542998 | |||||||
| chr15:65543054 | C | CAA | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-8621_88-8620ins others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65543054 | ||||||
| chr15:65543073 | T | TA | 10 | a0001c0001t0001g0102 a0001c0001t0002g0196 a0002c0003t0003g0227 others(7): Show |
10 | HG00544.hp1 HG00642.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.88-8587dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65543073 | ||||||
| chr15:65543143 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-8533G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543143 | |||||||
| chr15:65543183 | A | T | 1 | a0002c0003t0003g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.88-8493A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543183 | |||||||
| chr15:65543244 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.88-8432T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543244 | |||||||
| chr15:65543334 | C | CT | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-8333dupT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65543334 | ||||||
| chr15:65543383 | G | A | 1 | a0002c0003t0003g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.88-8293G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543383 | |||||||
| chr15:65543464 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(160): Show |
203 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.88-8212A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543464 | |||||||
| chr15:65543477 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.88-8199T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543477 | |||||||
| chr15:65543583 | T | C | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.88-8093T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543583 | |||||||
| chr15:65543711 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.88-7965T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543711 | |||||||
| chr15:65543746 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(219): Show |
274 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.88-7930C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543746 | |||||||
| chr15:65543838 | G | A | 3 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0015g0160 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.88-7838G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65543838 | |||||||
| chr15:65544033 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.88-7643C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544033 | |||||||
| chr15:65544051 | C | T | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-7625C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544051 | |||||||
| chr15:65544089 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0095 others(2): Show |
5 | NA18965.hp2 NA18977.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.88-7587A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544089 | |||||||
| chr15:65544099 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.88-7577C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544099 | |||||||
| chr15:65544487 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-7189G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544487 | |||||||
| chr15:65544518 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.88-7158T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544518 | |||||||
| chr15:65544693 | C | T | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.88-6983C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544693 | |||||||
| chr15:65544753 | G | T | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-6923G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544753 | |||||||
| chr15:65544837 | C | G | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.88-6839C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544837 | |||||||
| chr15:65544909 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.88-6767T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544909 | |||||||
| chr15:65544927 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.88-6749A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544927 | |||||||
| chr15:65544939 | T | C | 58 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(55): Show |
70 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.88-6737T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65544939 | |||||||
| chr15:65545106 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(160): Show |
203 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.88-6570C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545106 | |||||||
| chr15:65545108 | T | C | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-6568T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545108 | |||||||
| chr15:65545270 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
93 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.88-6406A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545270 | |||||||
| chr15:65545371 | C | CT | 1 | a0001c0001t0001g0005 | 3 | HG02071.hp1 NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.88-6304dupT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65545371 | ||||||
| chr15:65545455 | A | AT | 23 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0048 others(20): Show |
24 | HG01192.hp1 HG01978.hp1 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-6204dupT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65545455 | ||||||
| chr15:65545486 | G | A | 1 | a0002c0003t0003g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.88-6190G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545486 | |||||||
| chr15:65545536 | C | T | 3 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0015g0160 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.88-6140C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545536 | |||||||
| chr15:65545546 | C | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02145.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.88-6130C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545546 | |||||||
| chr15:65545585 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.88-6091A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545585 | |||||||
| chr15:65545589 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88-6087G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545589 | |||||||
| chr15:65545610 | AT | A | 28 | a0001c0001t0001g0090 a0001c0001t0001g0132 a0001c0001t0004g0033 others(25): Show |
29 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.88-6049delT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65545610 | ||||||
| chr15:65545610 | ATT | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(218): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.88-6050_88-6049del others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65545610 | ||||||
| chr15:65545733 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.88-5943C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545733 | |||||||
| chr15:65545744 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(224): Show |
279 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.88-5932C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545744 | |||||||
| chr15:65545746 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-5930T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545746 | |||||||
| chr15:65545759 | A | AT | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(217): Show |
272 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.88-5910dupT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65545759 | ||||||
| chr15:65545759 | A | ATT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0167 a0001c0001t0006g0222 others(4): Show |
7 | HG01109.hp2 HG01433.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.88-5911_88-5910dup others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65545759 | ||||||
| chr15:65545965 | C | T | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-5711C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65545965 | |||||||
| chr15:65546105 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88-5571C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65546105 | |||||||
| chr15:65546226 | TTTAAG | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(247): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.88-5442_88-5438del others(5): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65546226 | ||||||
| chr15:65546304 | A | G | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-5372A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65546304 | |||||||
| chr15:65546467 | A | G | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.88-5209A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65546467 | |||||||
| chr15:65546635 | C | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0211 |
3 | HG02145.hp2 HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.88-5041C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65546635 | |||||||
| chr15:65546656 | G | T | 1 | a0001c0001t0009g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.88-5020G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65546656 | |||||||
| chr15:65547033 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.88-4643G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547033 | |||||||
| chr15:65547140 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.88-4536G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547140 | |||||||
| chr15:65547207 | C | T | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.88-4469C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547207 | |||||||
| chr15:65547266 | G | A | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-4410G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547266 | |||||||
| chr15:65547336 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88-4340C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547336 | |||||||
| chr15:65547372 | C | T | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.88-4304C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547372 | |||||||
| chr15:65547404 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.88-4272C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547404 | |||||||
| chr15:65547705 | A | G | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-3971A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547705 | |||||||
| chr15:65547744 | C | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.88-3932C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547744 | |||||||
| chr15:65547840 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88-3836T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547840 | |||||||
| chr15:65547907 | G | T | 1 | a0001c0001t0001g0010 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.88-3769G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547907 | |||||||
| chr15:65547980 | A | G | 1 | a0001c0001t0007g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.88-3696A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65547980 | |||||||
| chr15:65548041 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.88-3635A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548041 | |||||||
| chr15:65548125 | A | G | 58 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(55): Show |
70 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.88-3551A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548125 | |||||||
| chr15:65548178 | T | C | 3 | a0002c0003t0003g0234 a0002c0003t0003g0235 a0002c0003t0003g0236 |
3 | HG02486.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.88-3498T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548178 | |||||||
| chr15:65548219 | T | A | 3 | a0002c0003t0003g0238 a0002c0003t0003g0243 a0002c0003t0003g0245 |
3 | HG02965.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.88-3457T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548219 | |||||||
| chr15:65548273 | G | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
93 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.88-3403G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548273 | |||||||
| chr15:65548307 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(155): Show |
197 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.88-3369G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548307 | |||||||
| chr15:65548364 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.88-3312T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548364 | |||||||
| chr15:65548512 | C | CA | 20 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0004g0033 others(17): Show |
21 | HG01167.hp1 HG01169.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.88-3145dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65548512 | ||||||
| chr15:65548512 | CA | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.88-3145delA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65548512 | ||||||
| chr15:65548530 | AAG | A | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-3144_88-3143del others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65548530 | ||||||
| chr15:65548534 | T | A | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-3142T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548534 | |||||||
| chr15:65548766 | A | G | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-2910A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548766 | |||||||
| chr15:65548987 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.88-2689C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65548987 | |||||||
| chr15:65549043 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
2 | HG02071.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.88-2633A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549043 | |||||||
| chr15:65549149 | C | T | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.88-2527C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549149 | |||||||
| chr15:65549165 | C | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(250): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.88-2511C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549165 | |||||||
| chr15:65549278 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.88-2398C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549278 | |||||||
| chr15:65549303 | C | T | 3 | a0002c0003t0003g0227 a0002c0003t0003g0232 a0002c0003t0003g0233 |
3 | HG02683.hp1 HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.88-2373C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549303 | |||||||
| chr15:65549426 | G | GA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.88-2226dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549426 | ||||||
| chr15:65549426 | G | GAA | 21 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0046 others(18): Show |
24 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-2227_88-2226dup others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549426 | ||||||
| chr15:65549426 | G | GAAA | 8 | a0001c0001t0004g0033 a0001c0001t0004g0260 a0001c0001t0004g0264 others(5): Show |
9 | HG01167.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.88-2228_88-2226dup others(3): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549426 | ||||||
| chr15:65549426 | GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0002g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88-2236_88-2226del others(11): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549426 | ||||||
| chr15:65549426 | GAAAAAAA others(5): Show |
G | 57 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(54): Show |
69 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.88-2237_88-2226del others(12): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549426 | ||||||
| chr15:65549469 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0007g0089 a0001c0001t0007g0169 others(6): Show |
10 | HG00621.hp2 HG02056.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.88-2207G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549469 | |||||||
| chr15:65549556 | C | T | 3 | a0001c0001t0002g0221 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02717.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.88-2120C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549556 | |||||||
| chr15:65549560 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.88-2116A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549560 | |||||||
| chr15:65549599 | C | CA | 15 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0097 others(12): Show |
16 | HG01346.hp1 HG01978.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.88-2056dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549599 | ||||||
| chr15:65549599 | C | CAA | 15 | a0001c0001t0004g0033 a0001c0001t0004g0036 a0001c0001t0004g0037 others(12): Show |
16 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.88-2057_88-2056dup others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549599 | ||||||
| chr15:65549599 | CA | C | 17 | a0001c0001t0001g0021 a0001c0001t0001g0049 a0001c0001t0001g0057 others(14): Show |
19 | HG00642.hp1 HG01070.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.88-2056delA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549599 | ||||||
| chr15:65549599 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-2064_88-2056del others(9): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65549599 | ||||||
| chr15:65549709 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.88-1967G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549709 | |||||||
| chr15:65549880 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.88-1796T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549880 | |||||||
| chr15:65549909 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.88-1767A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549909 | |||||||
| chr15:65549963 | C | A | 1 | a0001c0001t0004g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.88-1713C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65549963 | |||||||
| chr15:65550049 | A | G | 1 | a0001c0001t0004g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.88-1627A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65550049 | |||||||
| chr15:65550232 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.88-1444C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65550232 | |||||||
| chr15:65550318 | CAG | C | 4 | a0001c0002t0002g0185 a0001c0002t0002g0186 a0001c0002t0002g0207 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-1355_88-1354del others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 65550318 | ||||||
| chr15:65550640 | T | G | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.88-1036T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65550640 | |||||||
| chr15:65550816 | G | A | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-860G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65550816 | |||||||
| chr15:65550871 | T | C | 1 | a0002c0003t0003g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.88-805T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65550871 | |||||||
| chr15:65550995 | C | T | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.88-681C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65550995 | |||||||
| chr15:65551014 | G | C | 3 | a0002c0003t0003g0234 a0002c0003t0003g0235 a0002c0003t0003g0236 |
3 | HG02486.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.88-662G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65551014 | |||||||
| chr15:65551079 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.88-597C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65551079 | |||||||
| chr15:65551106 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.88-570A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65551106 | |||||||
| chr15:65551183 | C | T | 3 | a0002c0003t0003g0234 a0002c0003t0003g0235 a0002c0003t0003g0236 |
3 | HG02486.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.88-493C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65551183 | |||||||
| chr15:65551394 | G | T | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.88-282G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65551394 | |||||||
| chr15:65551424 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA18992.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.88-252G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 1/10 | chr15 | 65551424 | |||||||
| chr15:65551830 | C | T | 3 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0015g0160 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.130+112C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65551830 | |||||||
| chr15:65551983 | C | T | 17 | a0001c0001t0002g0024 a0001c0001t0002g0027 a0001c0001t0002g0028 others(14): Show |
21 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+265C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65551983 | |||||||
| chr15:65552291 | C | CT | 57 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(54): Show |
69 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.130+580dupT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 65552291 | ||||||
| chr15:65552298 | T | A | 3 | a0001c0001t0004g0267 a0001c0001t0006g0222 a0002c0003t0003g0236 |
3 | HG02055.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130+580T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552298 | |||||||
| chr15:65552299 | A | T | 3 | a0001c0001t0002g0206 a0001c0001t0009g0043 a0001c0001t0009g0044 |
3 | HG01517.hp1 HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.130+581A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552299 | |||||||
| chr15:65552404 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.130+686C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552404 | |||||||
| chr15:65552421 | C | T | 19 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(16): Show |
20 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.130+703C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552421 | |||||||
| chr15:65552626 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.130+908G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552626 | |||||||
| chr15:65552666 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.130+948T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552666 | |||||||
| chr15:65552667 | A | T | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+949A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552667 | |||||||
| chr15:65552687 | T | A | 19 | a0001c0001t0001g0134 a0001c0001t0004g0033 a0001c0001t0004g0035 others(16): Show |
20 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.130+969T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552687 | |||||||
| chr15:65552913 | A | C | 1 | a0001c0001t0001g0163 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.130+1195A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65552913 | |||||||
| chr15:65553016 | A | T | 1 | a0001c0001t0010g0269 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+1298A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553016 | |||||||
| chr15:65553125 | G | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0077 |
4 | HG00323.hp1 HG00738.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+1407G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553125 | |||||||
| chr15:65553164 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130+1446T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553164 | |||||||
| chr15:65553221 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0110 |
2 | NA18995.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.130+1503A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553221 | |||||||
| chr15:65553547 | T | C | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.131-1340T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553547 | |||||||
| chr15:65553666 | G | A | 1 | a0001c0001t0005g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.131-1221G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553666 | |||||||
| chr15:65553710 | A | C | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-1177A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553710 | |||||||
| chr15:65553713 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
278 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.131-1174T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553713 | |||||||
| chr15:65553730 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0094 |
4 | HG00609.hp2 HG00621.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-1157A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553730 | |||||||
| chr15:65553987 | C | T | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.131-900C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65553987 | |||||||
| chr15:65554260 | T | C | 2 | a0002c0003t0003g0227 a0002c0003t0003g0232 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.131-627T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65554260 | |||||||
| chr15:65554320 | T | TA | 6 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0189 others(3): Show |
6 | HG02615.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-566dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 65554320 | ||||||
| chr15:65554379 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0093 |
3 | HG02056.hp1 NA19004.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.131-508A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65554379 | |||||||
| chr15:65554685 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0112 a0001c0001t0001g0121 others(3): Show |
8 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-202G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65554685 | |||||||
| chr15:65554740 | A | G | 3 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0015g0160 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.131-147A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65554740 | |||||||
| chr15:65554818 | C | T | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-69C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 2/10 | chr15 | 65554818 | |||||||
| chr15:65554993 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.204+33T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65554993 | |||||||
| chr15:65555164 | A | G | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.204+204A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555164 | |||||||
| chr15:65555174 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.204+214A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555174 | |||||||
| chr15:65555198 | A | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.204+238A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555198 | |||||||
| chr15:65555258 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.204+298C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555258 | |||||||
| chr15:65555346 | C | T | 4 | a0001c0001t0002g0030 a0001c0001t0002g0196 a0001c0001t0002g0205 others(1): Show |
5 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+386C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555346 | |||||||
| chr15:65555469 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.204+509A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555469 | |||||||
| chr15:65555484 | T | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0105 |
2 | NA18968.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.204+524T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555484 | |||||||
| chr15:65555579 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.204+619C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555579 | |||||||
| chr15:65555580 | G | A | 3 | a0001c0001t0009g0034 a0001c0001t0009g0043 a0001c0001t0009g0044 |
3 | HG02647.hp1 HG03239.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.204+620G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555580 | |||||||
| chr15:65555584 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.204+624G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555584 | |||||||
| chr15:65555773 | A | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
93 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.204+813A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65555773 | |||||||
| chr15:65556256 | C | A | 7 | a0001c0001t0002g0027 a0001c0001t0002g0197 a0001c0001t0002g0206 others(4): Show |
8 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-483C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65556256 | |||||||
| chr15:65556331 | A | T | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.205-408A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | chr15 | 65556331 | |||||||
| chr15:65556460 | A | ATGGAGAG others(6): Show |
79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.205-277_205-265dup others(13): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 65556460 | ||||||
| chr15:65556985 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.369+82G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65556985 | |||||||
| chr15:65557046 | A | G | 19 | a0001c0001t0001g0015 a0001c0001t0001g0090 a0001c0001t0004g0033 others(16): Show |
21 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.369+143A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557046 | |||||||
| chr15:65557047 | G | A | 52 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(49): Show |
64 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.369+144G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557047 | |||||||
| chr15:65557214 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.369+311G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557214 | |||||||
| chr15:65557271 | A | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(260): Show |
317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.369+368A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557271 | |||||||
| chr15:65557332 | G | A | 1 | a0001c0001t0011g0159 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.369+429G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557332 | |||||||
| chr15:65557336 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
94 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.369+433G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557336 | |||||||
| chr15:65557392 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.369+489G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557392 | |||||||
| chr15:65557417 | G | A | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+514G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557417 | |||||||
| chr15:65557431 | C | A | 3 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0015g0160 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.369+528C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557431 | |||||||
| chr15:65557657 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.369+754G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557657 | |||||||
| chr15:65557939 | GT | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(222): Show |
277 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.370-724delT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 65557939 | ||||||
| chr15:65557979 | A | G | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.370-701A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65557979 | |||||||
| chr15:65558191 | A | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0203 |
3 | HG02258.hp1 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.370-489A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65558191 | |||||||
| chr15:65558377 | C | T | 1 | a0002c0003t0013g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.370-303C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65558377 | |||||||
| chr15:65558391 | C | T | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.370-289C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 4/10 | chr15 | 65558391 | |||||||
| chr15:65558812 | G | A | 5 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(2): Show |
5 | HG02630.hp2 HG02723.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.421+81G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65558812 | |||||||
| chr15:65558897 | C | T | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.421+166C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65558897 | |||||||
| chr15:65559047 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0203 |
3 | HG02258.hp1 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.421+316A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559047 | |||||||
| chr15:65559133 | A | C | 59 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(56): Show |
71 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.421+402A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559133 | |||||||
| chr15:65559470 | C | T | 1 | a0002c0003t0003g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.421+739C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559470 | |||||||
| chr15:65559472 | A | T | 1 | a0002c0003t0003g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.421+741A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559472 | |||||||
| chr15:65559593 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.421+862A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559593 | |||||||
| chr15:65559643 | T | C | 1 | a0001c0001t0011g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.421+912T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559643 | |||||||
| chr15:65559703 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.421+972C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559703 | |||||||
| chr15:65559798 | T | A | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.421+1067T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65559798 | |||||||
| chr15:65560047 | G | GT | 7 | a0001c0001t0001g0132 a0001c0001t0006g0247 a0001c0001t0006g0250 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+1329dupT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 65560047 | ||||||
| chr15:65560131 | C | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.421+1400C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65560131 | |||||||
| chr15:65560194 | A | G | 1 | a0001c0001t0006g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421+1463A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65560194 | |||||||
| chr15:65560278 | A | C | 4 | a0001c0001t0004g0033 a0001c0001t0004g0264 a0001c0001t0004g0265 others(1): Show |
5 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+1547A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65560278 | |||||||
| chr15:65560428 | T | G | 2 | a0001c0001t0010g0268 a0001c0001t0010g0269 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.421+1697T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65560428 | |||||||
| chr15:65560569 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.421+1838G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65560569 | |||||||
| chr15:65560801 | C | CA | 20 | a0001c0001t0001g0052 a0002c0003t0003g0032 a0002c0003t0003g0225 others(17): Show |
21 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.422-1955dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 65560801 | ||||||
| chr15:65560801 | CA | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
202 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.422-1955delA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 65560801 | ||||||
| chr15:65560968 | G | A | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.422-1806G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65560968 | |||||||
| chr15:65561076 | G | T | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-1698G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65561076 | |||||||
| chr15:65561202 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.422-1572C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65561202 | |||||||
| chr15:65561207 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.422-1567C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65561207 | |||||||
| chr15:65561248 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.422-1526C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65561248 | |||||||
| chr15:65561322 | C | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.422-1452C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65561322 | |||||||
| chr15:65561465 | C | CA | 6 | a0001c0001t0001g0008 a0001c0001t0001g0112 a0001c0001t0001g0121 others(3): Show |
8 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.422-1299dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 65561465 | ||||||
| chr15:65561668 | T | C | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.422-1106T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65561668 | |||||||
| chr15:65561865 | C | T | 1 | a0002c0003t0003g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.422-909C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65561865 | |||||||
| chr15:65562026 | C | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.422-748C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562026 | |||||||
| chr15:65562142 | G | A | 3 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0015g0160 |
3 | HG02698.hp1 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.422-632G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562142 | |||||||
| chr15:65562207 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0105 |
3 | NA18954.hp1 NA18968.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.422-567T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562207 | |||||||
| chr15:65562405 | CTG | C | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.422-367_422-366del others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 65562405 | ||||||
| chr15:65562448 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.422-326G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562448 | |||||||
| chr15:65562533 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.422-241A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562533 | |||||||
| chr15:65562561 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.422-213G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562561 | |||||||
| chr15:65562580 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.422-194G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562580 | |||||||
| chr15:65562686 | G | C | 3 | a0001c0001t0004g0033 a0001c0001t0004g0264 a0001c0001t0004g0267 |
4 | HG02055.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-88G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 5/10 | chr15 | 65562686 | |||||||
| chr15:65562983 | C | T | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+99C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65562983 | |||||||
| chr15:65563231 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.532+347A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563231 | |||||||
| chr15:65563452 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0090 |
3 | HG03017.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.532+568A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563452 | |||||||
| chr15:65563536 | G | C | 1 | a0001c0001t0002g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.532+652G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563536 | |||||||
| chr15:65563589 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.533-626C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563589 | |||||||
| chr15:65563652 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.533-563G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563652 | |||||||
| chr15:65563862 | C | T | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.533-353C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563862 | |||||||
| chr15:65563928 | C | A | 17 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.533-287C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563928 | |||||||
| chr15:65563994 | A | G | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.533-221A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65563994 | |||||||
| chr15:65564060 | C | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.533-155C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65564060 | |||||||
| chr15:65564121 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.533-94C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65564121 | |||||||
| chr15:65564131 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.533-84C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 6/10 | chr15 | 65564131 | |||||||
| chr15:65564467 | G | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
94 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.660+125G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65564467 | |||||||
| chr15:65564532 | C | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.660+190C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65564532 | |||||||
| chr15:65564556 | C | T | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.660+214C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65564556 | |||||||
| chr15:65564629 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0105 |
2 | NA18968.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.660+287A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65564629 | |||||||
| chr15:65564662 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.660+320G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65564662 | |||||||
| chr15:65564787 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.660+445A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65564787 | |||||||
| chr15:65564903 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.660+561G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65564903 | |||||||
| chr15:65565197 | C | T | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.660+855C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65565197 | |||||||
| chr15:65565210 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.660+868C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65565210 | |||||||
| chr15:65565314 | A | G | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.660+972A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65565314 | |||||||
| chr15:65565345 | G | C | 1 | a0002c0003t0003g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.660+1003G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65565345 | |||||||
| chr15:65565671 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.660+1329G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65565671 | |||||||
| chr15:65565817 | A | AG | 4 | a0001c0001t0004g0033 a0001c0001t0004g0264 a0001c0001t0004g0265 others(1): Show |
5 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+1475_660+1476i others(3): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65565817 | |||||||
| chr15:65565818 | A | G | 4 | a0001c0001t0004g0033 a0001c0001t0004g0264 a0001c0001t0004g0265 others(1): Show |
5 | HG02055.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+1476A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65565818 | |||||||
| chr15:65566284 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.660+1942G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566284 | |||||||
| chr15:65566318 | C | T | 2 | a0001c0001t0006g0250 a0001c0001t0006g0254 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.660+1976C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566318 | |||||||
| chr15:65566381 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.660+2039T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566381 | |||||||
| chr15:65566528 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.660+2186G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566528 | |||||||
| chr15:65566569 | C | T | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.660+2227C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566569 | |||||||
| chr15:65566691 | A | G | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+2349A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566691 | |||||||
| chr15:65566718 | T | C | 1 | a0001c0002t0002g0184 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.660+2376T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566718 | |||||||
| chr15:65566967 | T | G | 1 | a0001c0001t0002g0211 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.660+2625T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65566967 | |||||||
| chr15:65567148 | C | T | 7 | a0001c0001t0001g0064 a0001c0001t0001g0071 a0001c0001t0001g0072 others(4): Show |
7 | HG01070.hp2 HG01099.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+2806C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567148 | |||||||
| chr15:65567182 | T | C | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.660+2840T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567182 | |||||||
| chr15:65567225 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
325 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.661-2866G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567225 | |||||||
| chr15:65567300 | C | T | 81 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(78): Show |
94 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(91): Show |
intron_variant | MODIFIER | c.661-2791C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567300 | |||||||
| chr15:65567526 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.661-2565C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567526 | |||||||
| chr15:65567571 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.661-2520A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567571 | |||||||
| chr15:65567586 | C | A | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-2505C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567586 | |||||||
| chr15:65567734 | C | T | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.661-2357C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567734 | |||||||
| chr15:65567851 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.661-2240A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567851 | |||||||
| chr15:65567922 | GTTTC | G | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-2161_661-2158d others(6): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 65567922 | ||||||
| chr15:65567973 | A | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-2118A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65567973 | |||||||
| chr15:65568024 | G | A | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-2067G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568024 | |||||||
| chr15:65568169 | G | A | 1 | a0001c0001t0006g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.661-1922G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568169 | |||||||
| chr15:65568202 | G | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0067 |
2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.661-1889G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568202 | |||||||
| chr15:65568361 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA19000.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.661-1730T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568361 | |||||||
| chr15:65568461 | C | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0203 |
3 | HG02258.hp1 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.661-1630C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568461 | |||||||
| chr15:65568515 | C | T | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.661-1576C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568515 | |||||||
| chr15:65568578 | T | C | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-1513T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568578 | |||||||
| chr15:65568649 | G | A | 1 | a0001c0001t0006g0252 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.661-1442G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568649 | |||||||
| chr15:65568655 | A | G | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-1436A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568655 | |||||||
| chr15:65568659 | A | G | 28 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(25): Show |
29 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.661-1432A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568659 | |||||||
| chr15:65568715 | G | A | 3 | a0001c0001t0009g0034 a0001c0001t0009g0043 a0001c0001t0009g0044 |
3 | HG02647.hp1 HG03239.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.661-1376G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568715 | |||||||
| chr15:65568816 | G | C | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.661-1275G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568816 | |||||||
| chr15:65568870 | T | A | 1 | a0001c0001t0001g0010 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.661-1221T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65568870 | |||||||
| chr15:65569044 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.661-1047G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569044 | |||||||
| chr15:65569104 | T | C | 1 | a0001c0001t0004g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.661-987T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569104 | |||||||
| chr15:65569106 | A | G | 1 | a0001c0001t0004g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.661-985A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569106 | |||||||
| chr15:65569111 | G | A | 1 | a0001c0001t0004g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.661-980G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569111 | |||||||
| chr15:65569141 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.661-950G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569141 | |||||||
| chr15:65569247 | C | CA | 57 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0042 others(54): Show |
61 | HG00323.hp1 HG00642.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.661-830dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 65569247 | ||||||
| chr15:65569247 | C | CAA | 137 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
166 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.661-831_661-830dup others(2): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 65569247 | ||||||
| chr15:65569270 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.661-821A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569270 | |||||||
| chr15:65569471 | A | G | 1 | a0001c0001t0002g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.661-620A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569471 | |||||||
| chr15:65569473 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.661-618G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569473 | |||||||
| chr15:65569538 | G | A | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0008g0055 others(2): Show |
5 | NA18947.hp1 NA18949.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-553G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569538 | |||||||
| chr15:65569538 | G | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0103 |
2 | HG00735.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.661-553G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569538 | |||||||
| chr15:65569630 | C | T | 1 | a0001c0001t0004g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661-461C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569630 | |||||||
| chr15:65569661 | T | C | 1 | a0001c0002t0002g0201 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.661-430T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 7/10 | chr15 | 65569661 | |||||||
| chr15:65570562 | G | A | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.773+359G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 8/10 | chr15 | 65570562 | |||||||
| chr15:65570648 | C | T | 12 | a0001c0001t0004g0033 a0001c0001t0004g0260 a0001c0001t0004g0264 others(9): Show |
13 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.773+445C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 8/10 | chr15 | 65570648 | |||||||
| chr15:65570656 | A | G | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.773+453A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 8/10 | chr15 | 65570656 | |||||||
| chr15:65570808 | C | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.773+605C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 8/10 | chr15 | 65570808 | |||||||
| chr15:65570826 | T | C | 6 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0228 others(3): Show |
7 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.773+623T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 8/10 | chr15 | 65570826 | |||||||
| chr15:65570887 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.774-661C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 8/10 | chr15 | 65570887 | |||||||
| chr15:65571088 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0042 |
3 | HG01891.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.774-460T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 8/10 | chr15 | 65571088 | |||||||
| chr15:65572037 | C | G | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.881-198C>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 9/10 | chr15 | 65572037 | |||||||
| chr15:65572073 | G | C | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.881-162G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 9/10 | chr15 | 65572073 | |||||||
| chr15:65572203 | T | C | 1 | a0001c0001t0012g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.881-32T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 9/10 | chr15 | 65572203 | |||||||
| chr15:65572206 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.881-29T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 9/10 | chr15 | 65572206 | |||||||
| chr15:65572564 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1012+198T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572564 | |||||||
| chr15:65572601 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1012+235C>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572601 | |||||||
| chr15:65572637 | A | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1012+271A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572637 | |||||||
| chr15:65572914 | CA | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
82 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1012+564delA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 65572914 | ||||||
| chr15:65572919 | A | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1012+553A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572919 | |||||||
| chr15:65572923 | A | T | 23 | a0001c0001t0009g0034 a0002c0003t0003g0032 a0002c0003t0003g0225 others(20): Show |
24 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1012+557A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572923 | |||||||
| chr15:65572927 | A | AT | 19 | a0001c0001t0002g0024 a0001c0001t0002g0027 a0001c0001t0002g0028 others(16): Show |
23 | HG00140.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1012+561_1012+562i others(3): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572927 | |||||||
| chr15:65572927 | A | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
103 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1012+561A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572927 | |||||||
| chr15:65572930 | AT | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0152 |
4 | NA18941.hp2 NA18979.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+565delT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572930 | |||||||
| chr15:65572931 | T | A | 7 | a0001c0001t0001g0047 a0001c0001t0001g0111 a0001c0001t0001g0166 others(4): Show |
7 | HG02280.hp1 HG02602.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1012+565T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572931 | |||||||
| chr15:65572950 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0155 |
2 | NA18983.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1012+584T>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572950 | |||||||
| chr15:65572950 | T | TA | 18 | a0001c0001t0004g0033 a0001c0001t0004g0035 a0001c0001t0004g0036 others(15): Show |
19 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1012+596dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 65572950 | ||||||
| chr15:65572983 | G | C | 1 | a0001c0001t0011g0159 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1012+617G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65572983 | |||||||
| chr15:65573133 | T | C | 1 | a0001c0001t0006g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1012+767T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573133 | |||||||
| chr15:65573270 | G | C | 1 | a0002c0003t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1012+904G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573270 | |||||||
| chr15:65573294 | T | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(190): Show |
226 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.1012+928T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573294 | |||||||
| chr15:65573297 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0166 |
2 | NA18999.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1012+931G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573297 | |||||||
| chr15:65573400 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1012+1034A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573400 | |||||||
| chr15:65573471 | G | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01099.hp2 HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1012+1105G>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573471 | |||||||
| chr15:65573572 | C | T | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1012+1206C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573572 | |||||||
| chr15:65573607 | C | CA | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(259): Show |
315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1012+1255dupA | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 65573607 | ||||||
| chr15:65573781 | A | G | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1012+1415A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573781 | |||||||
| chr15:65573978 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1012+1612C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65573978 | |||||||
| chr15:65574366 | A | G | 2 | a0001c0001t0009g0043 a0001c0001t0009g0044 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1013-1937A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574366 | |||||||
| chr15:65574396 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1013-1907A>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574396 | |||||||
| chr15:65574437 | C | T | 58 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(55): Show |
70 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.1013-1866C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574437 | |||||||
| chr15:65574541 | A | C | 1 | a0001c0001t0006g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1013-1762A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574541 | |||||||
| chr15:65574591 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1013-1712T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574591 | |||||||
| chr15:65574600 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02145.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1013-1703C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574600 | |||||||
| chr15:65574615 | A | C | 1 | a0003c0004t0019g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1013-1688A>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574615 | |||||||
| chr15:65574706 | G | T | 58 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(55): Show |
70 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.1013-1597G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574706 | |||||||
| chr15:65574713 | ATTTC | A | 64 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(61): Show |
76 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.1013-1582_1013-157 others(8): Show |
HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 65574713 | ||||||
| chr15:65574928 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1013-1375G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65574928 | |||||||
| chr15:65575188 | G | GT | 23 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0042 others(20): Show |
26 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1013-1098dupT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 65575188 | ||||||
| chr15:65575189 | T | G | 56 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0027 others(53): Show |
67 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1013-1114T>G | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575189 | |||||||
| chr15:65575230 | C | T | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1013-1073C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575230 | |||||||
| chr15:65575382 | G | A | 1 | a0001c0001t0007g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1013-921G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575382 | |||||||
| chr15:65575395 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1013-908C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575395 | |||||||
| chr15:65575480 | G | T | 1 | a0001c0002t0002g0191 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1013-823G>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575480 | |||||||
| chr15:65575564 | CT | C | 6 | a0001c0001t0006g0247 a0001c0001t0006g0250 a0001c0001t0006g0251 others(3): Show |
6 | HG02630.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1013-738delT | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575564 | |||||||
| chr15:65575649 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1013-654A>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575649 | |||||||
| chr15:65575669 | G | A | 58 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0026 others(55): Show |
70 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.1013-634G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575669 | |||||||
| chr15:65575701 | T | C | 22 | a0002c0003t0003g0032 a0002c0003t0003g0225 a0002c0003t0003g0226 others(19): Show |
23 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1013-602T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575701 | |||||||
| chr15:65575762 | C | T | 1 | a0001c0001t0011g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1013-541C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575762 | |||||||
| chr15:65575958 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1013-345G>A | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65575958 | |||||||
| chr15:65576150 | T | C | 1 | a0002c0003t0003g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1013-153T>C | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65576150 | |||||||
| chr15:65576287 | C | T | 1 | a0001c0001t0009g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1013-16C>T | HACD3 | ENSG00000074696.13 | transcript | ENST00000261875.10 | protein_coding | 10/10 | chr15 | 65576287 |