Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26130 |
| ensemblid | ENSG00000165219.23 |
| hgncid | 23375 |
| symbol | GAPVD1 |
| name | GTPase activating protein and VPS9 domains 1 |
| refseq_nuc | NM_001282680.3 |
| refseq_prot | NP_001269609.1 |
| ensembl_nuc | ENST00000297933.11 |
| ensembl_prot | ENSP00000297933.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 125261826 |
| end | 125367207 |
| strand | + |
| ver | v1.2 |
| region | chr9:125261826-125367207 |
| region5000 | chr9:125256826-125372207 |
| regionname0 | GAPVD1_chr9_125261826_125367207 |
| regionname5000 | GAPVD1_chr9_125256826_125372207 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1460 | 332 | 66 | 53 | 166 | 12 | 33 | 128 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | MVKLD others(1455): Show |
chr9 | 125256826 | 125372207 |
| a0002 | 0/0 | 1460 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | MVKLD others(1455): Show |
chr9 | 125256826 | 125372207 |
| a0003 | 0/0 | 1460 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | MVKLD others(1455): Show |
chr9 | 125256826 | 125372207 |
| a0004 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | MVKLD others(1455): Show |
chr9 | 125256826 | 125372207 |
| a0005 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | MVKLD others(1455): Show |
chr9 | 125256826 | 125372207 |
| a0006 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | MVKLD others(1455): Show |
chr9 | 125256826 | 125372207 |
| a0007 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | MVKLD others(1455): Show |
chr9 | 125256826 | 125372207 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4380 | 271 | 51 | 41 | 140 | 10 | 28 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0002 | 0/0 | 4380 | 31 | 0 | 6 | 24 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0003 | 0/0 | 4380 | 17 | 14 | 2 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0004 | 1/0 | 4380 | 4 | 0 | 2 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0005 | 0/0 | 4380 | 3 | 0 | 1 | 0 | 1 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0009 | 0/0 | 4380 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0010 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0012 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0013 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0014 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0001c0016 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0002c0006 | 0/0 | 4380 | 2 | 1 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0003c0007 | 0/0 | 4380 | 2 | 0 | 0 | 0 | 0 | 2 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0004c0008 | 0/0 | 4380 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0005c0017 | 0/0 | 4380 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0006c0011 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 | ||
| a0007c0015 | 0/0 | 4380 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | ATGGT others(4375): Show |
chr9 | 125256826 | 125372207 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9177 | 120 | 33 | 15 | 55 | 2 | 15 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0002 | 0/0 | 9176 | 92 | 3 | 11 | 62 | 6 | 10 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0004 | 0/0 | 9176 | 9 | 7 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0005 | 0/0 | 9177 | 12 | 0 | 0 | 12 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0008 | 0/0 | 9176 | 5 | 0 | 5 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0009 | 0/0 | 9175 | 3 | 3 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9170): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0010 | 0/0 | 9177 | 3 | 0 | 1 | 0 | 2 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0012 | 0/0 | 9176 | 2 | 0 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0013 | 0/0 | 9176 | 2 | 1 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0014 | 0/1 | 9177 | 2 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0015 | 0/0 | 9175 | 2 | 0 | 0 | 1 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9170): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0016 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0017 | 0/0 | 9176 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0019 | 0/0 | 9176 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0020 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0021 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0022 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0023 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0024 | 0/0 | 9177 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0025 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0027 | 0/0 | 9175 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9170): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0028 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0029 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0030 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0031 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0032 | 0/0 | 9177 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0033 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0034 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0035 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0001t0036 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0002t0003 | 0/0 | 9177 | 20 | 0 | 0 | 19 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0002t0007 | 0/0 | 9176 | 10 | 0 | 5 | 5 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0002t0038 | 0/0 | 9176 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0003t0004 | 0/0 | 9176 | 4 | 4 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0003t0006 | 0/0 | 9175 | 11 | 8 | 2 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9170): Show |
chr9 | 125256826 | 125372207 |
| a0001c0003t0018 | 0/0 | 9176 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0003t0026 | 0/0 | 9175 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9170): Show |
chr9 | 125256826 | 125372207 |
| a0001c0004t0001 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0004t0002 | 1/0 | 9176 | 3 | 0 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0005t0001 | 0/0 | 9177 | 3 | 0 | 1 | 0 | 1 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0009t0001 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0010t0006 | 0/0 | 9175 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9170): Show |
chr9 | 125256826 | 125372207 |
| a0001c0012t0001 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0013t0002 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0001c0014t0001 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0001c0016t0037 | 0/0 | 9175 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9170): Show |
chr9 | 125256826 | 125372207 |
| a0002c0006t0011 | 0/0 | 9176 | 2 | 1 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0003c0007t0001 | 0/0 | 9177 | 2 | 0 | 0 | 0 | 0 | 2 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0004c0008t0002 | 0/0 | 9176 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| a0005c0017t0001 | 0/0 | 9177 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0006c0011t0005 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9172): Show |
chr9 | 125256826 | 125372207 |
| a0007c0015t0002 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | GCAGG others(9171): Show |
chr9 | 125256826 | 125372207 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0009g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0010g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0010g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0012g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0012g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0013g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0013g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0014g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0014g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0015g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0016g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0017g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0020g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0021g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0022g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0023g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0025g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0027g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0028g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0029g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0030g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0031g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0032g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0033g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0034g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0035g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0036g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0038g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0018g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0026g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0002g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0005t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0009t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0010t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0012t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0013t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0014t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0016t0037g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0002c0006t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0002c0006t0011g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0003c0007t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0003c0007t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0004c0008t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0005c0017t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0006c0011t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0007c0015t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0035 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00280 | hp1 | a0001 | c0005 | t0001 | g0224 | EUR | FIN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | FIN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00544 | hp2 | a0001 | c0002 | t0007 | g0161 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00558 | hp2 | a0001 | c0001 | t0027 | g0221 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0163 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00642 | hp1 | a0001 | c0001 | t0012 | g0102 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00673 | hp1 | a0001 | c0001 | t0029 | g0077 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00733 | hp1 | a0001 | c0001 | t0025 | g0205 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00738 | hp1 | a0001 | c0001 | t0021 | g0188 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0103 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00741 | hp2 | a0001 | c0001 | t0014 | g0260 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0046 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01081 | hp2 | a0001 | c0002 | t0007 | g0148 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01109 | hp1 | a0001 | c0003 | t0006 | g0126 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01109 | hp2 | a0002 | c0006 | t0011 | g0143 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01167 | hp1 | a0001 | c0003 | t0006 | g0132 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0253 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01243 | hp2 | a0001 | c0009 | t0001 | g0189 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01255 | hp2 | a0001 | c0002 | t0007 | g0001 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01257 | hp1 | a0001 | c0002 | t0038 | g0001 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0117 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01358 | hp2 | a0001 | c0001 | t0016 | g0053 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0054 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01361 | hp2 | a0001 | c0002 | t0007 | g0145 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0115 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0047 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0263 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01517 | hp1 | a0001 | c0001 | t0010 | g0213 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0038 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01884 | hp1 | a0001 | c0003 | t0006 | g0123 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01993 | hp2 | a0001 | c0002 | t0007 | g0153 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02004 | hp1 | a0001 | c0001 | t0023 | g0301 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02004 | hp2 | a0001 | c0005 | t0001 | g0216 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0144 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02055 | hp2 | a0001 | c0003 | t0026 | g0129 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0339 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0152 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02132 | hp2 | a0001 | c0001 | t0031 | g0105 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02135 | hp1 | a0001 | c0001 | t0030 | g0141 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | CDX | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CDX | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02258 | hp1 | a0001 | c0003 | t0018 | g0131 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02280 | hp2 | a0001 | c0003 | t0006 | g0125 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0034 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02451 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02572 | hp2 | a0001 | c0003 | t0006 | g0127 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02602 | hp1 | a0004 | c0008 | t0002 | g0086 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02622 | hp1 | a0001 | c0003 | t0004 | g0136 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0014 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02683 | hp1 | a0001 | c0016 | t0037 | g0171 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02717 | hp2 | a0001 | c0001 | t0013 | g0196 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02723 | hp2 | a0005 | c0017 | t0001 | g0249 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02735 | hp1 | a0001 | c0001 | t0034 | g0214 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02895 | hp2 | a0001 | c0003 | t0006 | g0135 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02897 | hp1 | a0001 | c0003 | t0006 | g0138 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02897 | hp2 | a0001 | c0001 | t0019 | g0207 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02922 | hp2 | a0001 | c0003 | t0006 | g0124 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03017 | hp2 | a0003 | c0007 | t0001 | g0307 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0193 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03098 | hp1 | a0002 | c0006 | t0011 | g0142 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0134 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03486 | hp1 | a0001 | c0001 | t0032 | g0294 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0130 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03540 | hp1 | a0001 | c0003 | t0006 | g0137 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03654 | hp1 | a0001 | c0001 | t0022 | g0280 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03704 | hp1 | a0003 | c0007 | t0001 | g0300 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03710 | hp2 | a0001 | c0003 | t0006 | g0128 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0197 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04184 | hp2 | a0001 | c0012 | t0001 | g0285 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0147 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0330 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18949 | hp2 | a0001 | c0002 | t0003 | g0155 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18954 | hp2 | a0001 | c0001 | t0035 | g0304 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18957 | hp2 | a0001 | c0014 | t0001 | g0231 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18959 | hp2 | a0001 | c0013 | t0002 | g0048 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0338 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18962 | hp1 | a0001 | c0001 | t0036 | g0091 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18962 | hp2 | a0001 | c0001 | t0020 | g0333 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18964 | hp1 | a0001 | c0002 | t0007 | g0162 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0164 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18967 | hp2 | a0001 | c0001 | t0028 | g0113 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18968 | hp1 | a0001 | c0002 | t0007 | g0151 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18974 | hp1 | a0006 | c0011 | t0005 | g0336 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18986 | hp1 | a0007 | c0015 | t0002 | g0049 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18991 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0149 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19043 | hp2 | a0001 | c0010 | t0006 | g0133 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19054 | hp1 | a0001 | c0002 | t0007 | g0150 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19060 | hp2 | a0001 | c0001 | t0015 | g0063 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19087 | hp2 | a0001 | c0002 | t0007 | g0168 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19088 | hp1 | a0001 | c0001 | t0033 | g0039 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19089 | hp2 | a0001 | c0001 | t0013 | g0190 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ASW | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | TSI | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0088 | EUR | TSI | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20905 | hp1 | a0001 | c0001 | t0015 | g0067 | SAS | GIH | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | GIH | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01123 | hp1 | a0001 | c0002 | t0007 | g0169 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0057 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0014 | g0267 | REF | REF | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0002 | g0022 | REF | REF | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125302143 | G | T | 1 | a0003 | 2 | HG03017.hp2 HG03704.hp1 |
missense_variant | MODERATE | c.346G>T | p.Ala116Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 678/9176 | 346/4383 | 116/1460 | chr9 | 125302143 | |||
| chr9:125302647 | G | A | 1 | a0004 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.850G>A | p.Val284Met | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 1182/9176 | 850/4383 | 284/1460 | chr9 | 125302647 | |||
| chr9:125307821 | A | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1382A>G | p.Asn461Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/28 | 1714/9176 | 1382/4383 | 461/1460 | chr9 | 125307821 | |||
| chr9:125321493 | C | A | 1 | a0006 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1663C>A | p.Leu555Ile | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/28 | 1995/9176 | 1663/4383 | 555/1460 | chr9 | 125321493 | |||
| chr9:125321494 | T | C | 1 | a0006 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1664T>C | p.Leu555Pro | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/28 | 1996/9176 | 1664/4383 | 555/1460 | chr9 | 125321494 | |||
| chr9:125326463 | C | T | 1 | a0007 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.1906C>T | p.Arg636Cys | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/28 | 2238/9176 | 1906/4383 | 636/1460 | chr9 | 125326463 | |||
| chr9:125337505 | C | T | 1 | a0002 | 2 | HG01109.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.2791C>T | p.Pro931Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/28 | 3123/9176 | 2791/4383 | 931/1460 | chr9 | 125337505 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125302394 | T | G | 1 | a0001c0002 | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
synonymous_variant | LOW | c.597T>G | p.Thr199Thr | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 929/9176 | 597/4383 | 199/1460 | chr9 | 125302394 | |||
| chr9:125302676 | T | C | 1 | a0001c0009 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.879T>C | p.Cys293Cys | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 1211/9176 | 879/4383 | 293/1460 | chr9 | 125302676 | |||
| chr9:125305140 | G | A | 2 | a0001c0003 a0001c0010 |
18 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(15): Show |
synonymous_variant | LOW | c.1107G>A | p.Lys369Lys | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/28 | 1439/9176 | 1107/4383 | 369/1460 | chr9 | 125305140 | |||
| chr9:125307424 | C | A | 1 | a0001c0005 | 3 | HG00280.hp1 HG02004.hp2 HG04184.hp1 |
synonymous_variant | LOW | c.1128C>A | p.Ala376Ala | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 7/28 | 1460/9176 | 1128/4383 | 376/1460 | chr9 | 125307424 | |||
| chr9:125312468 | C | T | 1 | a0001c0016 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1458C>T | p.Ser486Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/28 | 1790/9176 | 1458/4383 | 486/1460 | chr9 | 125312468 | |||
| chr9:125312528 | T | C | 16 | a0001c0001 a0001c0002 a0001c0003 others(13): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
synonymous_variant | LOW | c.1518T>C | p.Ile506Ile | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/28 | 1850/9176 | 1518/4383 | 506/1460 | chr9 | 125312528 | |||
| chr9:125321495 | C | T | 1 | a0006c0011 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1665C>T | p.Leu555Leu | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/28 | 1997/9176 | 1665/4383 | 555/1460 | chr9 | 125321495 | |||
| chr9:125330154 | T | C | 1 | a0001c0012 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2109T>C | p.Thr703Thr | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/28 | 2441/9176 | 2109/4383 | 703/1460 | chr9 | 125330154 | |||
| chr9:125350855 | G | C | 1 | a0001c0013 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.3552G>C | p.Ser1184Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/28 | 3884/9176 | 3552/4383 | 1184/1460 | chr9 | 125350855 | |||
| chr9:125355660 | C | T | 1 | a0001c0010 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.3774C>T | p.Thr1258Thr | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/28 | 4106/9176 | 3774/4383 | 1258/1460 | chr9 | 125355660 | |||
| chr9:125362614 | A | G | 1 | a0001c0014 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.4251A>G | p.Pro1417Pro | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4583/9176 | 4251/4383 | 1417/1460 | chr9 | 125362614 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125261865 | C | G | 3 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0038 |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-293C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/28 | 37057 | chr9 | 125261865 | ||||||
| chr9:125261952 | C | G | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-206C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/28 | 36970 | chr9 | 125261952 | ||||||
| chr9:125295535 | C | T | 1 | a0001c0001t0036 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/28 | 3387 | chr9 | 125295535 | ||||||
| chr9:125362859 | A | G | 1 | a0001c0001t0035 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 113 | chr9 | 125362859 | ||||||
| chr9:125363149 | A | G | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 403 | chr9 | 125363149 | ||||||
| chr9:125363198 | C | T | 1 | a0001c0001t0034 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 452 | chr9 | 125363198 | ||||||
| chr9:125363228 | C | T | 1 | a0001c0001t0008 | 5 | HG01123.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*482C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 482 | chr9 | 125363228 | ||||||
| chr9:125363471 | G | A | 1 | a0001c0001t0008 | 5 | HG01123.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*725G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 725 | chr9 | 125363471 | ||||||
| chr9:125363767 | C | G | 1 | a0001c0001t0033 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1021C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1021 | chr9 | 125363767 | ||||||
| chr9:125363919 | A | G | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1173A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1173 | chr9 | 125363919 | ||||||
| chr9:125364032 | C | T | 1 | a0001c0001t0032 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1286C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1286 | chr9 | 125364032 | ||||||
| chr9:125364064 | T | A | 6 | a0001c0001t0016 a0001c0002t0003 a0001c0002t0007 others(3): Show |
35 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1318T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1318 | chr9 | 125364064 | ||||||
| chr9:125364096 | G | A | 1 | a0001c0001t0012 | 2 | HG00642.hp1 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1350G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1350 | chr9 | 125364096 | ||||||
| chr9:125364103 | G | A | 4 | a0001c0001t0016 a0001c0002t0003 a0001c0002t0007 others(1): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1357G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1357 | chr9 | 125364103 | ||||||
| chr9:125364368 | G | C | 37 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(34): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*1622G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1622 | chr9 | 125364368 | ||||||
| chr9:125364382 | C | G | 1 | a0001c0001t0031 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1636C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1636 | chr9 | 125364382 | ||||||
| chr9:125364672 | C | T | 1 | a0002c0006t0011 | 2 | HG01109.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1926C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1926 | chr9 | 125364672 | ||||||
| chr9:125364758 | G | A | 1 | a0001c0001t0009 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2012G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2012 | chr9 | 125364758 | ||||||
| chr9:125364832 | C | T | 1 | a0001c0003t0026 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2086C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2086 | chr9 | 125364832 | ||||||
| chr9:125365059 | G | T | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2313G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2313 | chr9 | 125365059 | ||||||
| chr9:125365133 | A | G | 30 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(27): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2387A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2387 | chr9 | 125365133 | ||||||
| chr9:125365318 | A | AT | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(20): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*2589dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2590 | INFO_REALIGN_3_PRIME | chr9 | 125365318 | |||||
| chr9:125365318 | AT | A | 7 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0027 others(4): Show |
20 | HG00558.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2589delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2589 | INFO_REALIGN_3_PRIME | chr9 | 125365318 | |||||
| chr9:125365724 | C | T | 3 | a0001c0001t0005 a0001c0001t0020 a0006c0011t0005 |
14 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2978C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2978 | chr9 | 125365724 | ||||||
| chr9:125365737 | C | G | 1 | a0001c0001t0010 | 3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2991C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2991 | chr9 | 125365737 | ||||||
| chr9:125365805 | A | T | 1 | a0001c0001t0027 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3059A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3059 | chr9 | 125365805 | ||||||
| chr9:125365928 | C | T | 1 | a0001c0001t0025 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3182 | chr9 | 125365928 | ||||||
| chr9:125366148 | A | G | 1 | a0001c0001t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3402A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3402 | chr9 | 125366148 | ||||||
| chr9:125366207 | C | T | 1 | a0001c0001t0029 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3461C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3461 | chr9 | 125366207 | ||||||
| chr9:125366229 | G | A | 1 | a0001c0001t0009 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3483G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3483 | chr9 | 125366229 | ||||||
| chr9:125366239 | G | A | 1 | a0001c0002t0038 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3493G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3493 | chr9 | 125366239 | ||||||
| chr9:125366290 | C | T | 1 | a0001c0001t0019 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3544C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3544 | chr9 | 125366290 | ||||||
| chr9:125366291 | G | A | 1 | a0001c0001t0017 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3545G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3545 | chr9 | 125366291 | ||||||
| chr9:125366339 | G | A | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3593G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3593 | chr9 | 125366339 | ||||||
| chr9:125366503 | A | G | 30 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(27): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*3757A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3757 | chr9 | 125366503 | ||||||
| chr9:125366517 | T | C | 1 | a0001c0001t0021 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3771T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3771 | chr9 | 125366517 | ||||||
| chr9:125366545 | C | T | 1 | a0001c0001t0024 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3799C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3799 | chr9 | 125366545 | ||||||
| chr9:125366584 | C | T | 1 | a0001c0001t0023 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3838C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3838 | chr9 | 125366584 | ||||||
| chr9:125366833 | A | G | 1 | a0001c0001t0022 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4087A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4087 | chr9 | 125366833 | ||||||
| chr9:125366848 | A | G | 1 | a0001c0003t0018 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4102A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4102 | chr9 | 125366848 | ||||||
| chr9:125366955 | G | A | 1 | a0001c0001t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4209G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4209 | chr9 | 125366955 | ||||||
| chr9:125367107 | T | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4361T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4361 | chr9 | 125367107 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125262019 | G | T | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-199+60G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262019 | |||||||
| chr9:125262038 | G | T | 1 | a0001c0001t0005g0339 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-199+79G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262038 | |||||||
| chr9:125262102 | T | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-199+143T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262102 | |||||||
| chr9:125262168 | G | A | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-199+209G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262168 | |||||||
| chr9:125262632 | CT | C | 13 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(10): Show |
13 | HG00558.hp1 HG02027.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-199+674delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262632 | |||||||
| chr9:125262714 | G | A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
5 | HG02027.hp2 NA18943.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199+755G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262714 | |||||||
| chr9:125263081 | T | A | 1 | a0001c0001t0021g0188 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-199+1122T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263081 | |||||||
| chr9:125263146 | G | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-199+1187G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263146 | |||||||
| chr9:125263215 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-199+1256C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263215 | |||||||
| chr9:125263255 | C | G | 14 | a0001c0001t0001g0326 a0001c0001t0005g0327 a0001c0001t0005g0328 others(11): Show |
14 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-199+1296C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263255 | |||||||
| chr9:125263321 | T | C | 2 | a0001c0002t0003g0005 a0001c0002t0003g0006 |
2 | NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-199+1362T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263321 | |||||||
| chr9:125263390 | A | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-199+1431A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263390 | |||||||
| chr9:125263406 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-199+1447G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263406 | |||||||
| chr9:125263478 | A | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-199+1519A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263478 | |||||||
| chr9:125263528 | G | GT | 7 | a0001c0001t0001g0283 a0001c0001t0002g0106 a0001c0001t0002g0139 others(4): Show |
7 | HG00621.hp2 HG01099.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-199+1582dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125263528 | ||||||
| chr9:125263528 | G | T | 17 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(14): Show |
17 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-199+1569G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263528 | |||||||
| chr9:125263618 | G | A | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG01069.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199+1659G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263618 | |||||||
| chr9:125263683 | ACAGCACT others(20): Show |
A | 199 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-199+1756_-199+178 others(31): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125263683 | ||||||
| chr9:125263907 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-199+1948A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263907 | |||||||
| chr9:125263908 | A | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA19054.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-199+1949A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263908 | |||||||
| chr9:125263984 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0016 |
2 | NA18977.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-199+2025G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263984 | |||||||
| chr9:125263999 | G | T | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-199+2040G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263999 | |||||||
| chr9:125264117 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-199+2158C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264117 | |||||||
| chr9:125264129 | C | T | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(2): Show |
5 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199+2170C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264129 | |||||||
| chr9:125264138 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-199+2179C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264138 | |||||||
| chr9:125264208 | G | A | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-199+2249G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264208 | |||||||
| chr9:125264565 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-199+2606C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264565 | |||||||
| chr9:125264718 | AT | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0191 a0001c0001t0002g0017 others(3): Show |
6 | HG01099.hp2 HG01243.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199+2775delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125264718 | ||||||
| chr9:125264781 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-199+2822C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264781 | |||||||
| chr9:125264924 | G | A | 2 | a0001c0003t0004g0020 a0001c0003t0004g0021 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-199+2965G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264924 | |||||||
| chr9:125264987 | A | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199+3028A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264987 | |||||||
| chr9:125265039 | C | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-199+3080C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265039 | |||||||
| chr9:125265227 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-199+3268C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265227 | |||||||
| chr9:125265428 | C | T | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-199+3469C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265428 | |||||||
| chr9:125265524 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-198-3412C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265524 | |||||||
| chr9:125265566 | G | A | 91 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0195 others(88): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-198-3370G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265566 | |||||||
| chr9:125265588 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-198-3348T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265588 | |||||||
| chr9:125265628 | G | A | 1 | a0001c0001t0024g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-198-3308G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265628 | |||||||
| chr9:125265636 | C | CTCCTGAC others(827): Show |
1 | a0001c0001t0001g0268 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(838): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(832): Show |
1 | a0001c0001t0001g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(843): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
122 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0314 others(119): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(832): Show |
1 | a0001c0001t0002g0118 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(843): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(832): Show |
1 | a0001c0001t0002g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(843): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(831): Show |
2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | NA18949.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265636 | C | CTCCTGAC others(828): Show |
2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | NA19079.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(839): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | ||||||
| chr9:125265836 | G | A | 1 | a0001c0002t0003g0144 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-198-3100G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265836 | |||||||
| chr9:125265924 | T | TA | 9 | a0001c0001t0001g0194 a0001c0001t0001g0266 a0001c0001t0001g0269 others(6): Show |
9 | HG01358.hp1 HG01361.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-198-2995dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265924 | ||||||
| chr9:125265924 | TA | T | 13 | a0001c0001t0001g0191 a0001c0001t0001g0265 a0001c0001t0001g0312 others(10): Show |
13 | HG01515.hp2 HG01884.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-198-2995delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265924 | ||||||
| chr9:125265972 | G | A | 228 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(225): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.-198-2964G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265972 | |||||||
| chr9:125266074 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-198-2862C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266074 | |||||||
| chr9:125266127 | AT | A | 193 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(190): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-198-2793delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125266127 | ||||||
| chr9:125266145 | A | T | 1 | a0001c0001t0008g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-198-2791A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266145 | |||||||
| chr9:125266166 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-198-2770G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266166 | |||||||
| chr9:125266190 | G | A | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-198-2746G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266190 | |||||||
| chr9:125266277 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-198-2659C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266277 | |||||||
| chr9:125266294 | T | TTTTTA | 5 | a0001c0001t0004g0007 a0001c0001t0009g0002 a0001c0001t0009g0003 others(2): Show |
5 | HG01884.hp2 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-198-2617_-198-261 others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125266294 | ||||||
| chr9:125266319 | A | T | 1 | a0001c0001t0008g0115 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-198-2617A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266319 | |||||||
| chr9:125266324 | T | A | 234 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(231): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-198-2612T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266324 | |||||||
| chr9:125266336 | C | T | 14 | a0001c0001t0001g0299 a0001c0001t0001g0302 a0001c0001t0001g0303 others(11): Show |
14 | HG02004.hp1 HG02056.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.-198-2600C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266336 | |||||||
| chr9:125266529 | G | C | 18 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-198-2407G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266529 | |||||||
| chr9:125266532 | C | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-198-2404C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266532 | |||||||
| chr9:125266579 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-198-2357C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266579 | |||||||
| chr9:125266604 | C | T | 33 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0024 others(30): Show |
33 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-198-2332C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266604 | |||||||
| chr9:125266605 | G | A | 43 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(40): Show |
43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.-198-2331G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266605 | |||||||
| chr9:125266662 | A | G | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-198-2274A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266662 | |||||||
| chr9:125266733 | C | T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-198-2203C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266733 | |||||||
| chr9:125266748 | C | G | 1 | a0004c0008t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-198-2188C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266748 | |||||||
| chr9:125266908 | G | A | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-198-2028G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266908 | |||||||
| chr9:125267238 | C | T | 6 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-198-1698C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267238 | |||||||
| chr9:125267408 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-198-1528G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267408 | |||||||
| chr9:125267720 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-198-1216G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267720 | |||||||
| chr9:125267794 | A | G | 1 | a0001c0002t0007g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-198-1142A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267794 | |||||||
| chr9:125268194 | AC | A | 122 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0195 others(119): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-198-731delC | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268194 | ||||||
| chr9:125268205 | C | A | 4 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 others(1): Show |
4 | HG02559.hp2 HG04184.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-198-731C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125268205 | |||||||
| chr9:125268205 | C | CA | 5 | a0001c0001t0001g0180 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
5 | HG00438.hp1 HG02056.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-198-722dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268205 | ||||||
| chr9:125268206 | A | C | 1 | a0001c0001t0001g0293 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-198-730A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125268206 | |||||||
| chr9:125268495 | G | GT | 28 | a0001c0001t0001g0179 a0001c0001t0001g0291 a0001c0001t0001g0292 others(25): Show |
28 | HG00423.hp1 HG00741.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-198-420dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268495 | ||||||
| chr9:125268495 | GT | G | 8 | a0001c0001t0001g0198 a0001c0001t0002g0199 a0001c0001t0005g0327 others(5): Show |
8 | HG01167.hp1 HG02109.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-198-420delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268495 | ||||||
| chr9:125268558 | A | G | 203 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(200): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-198-378A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125268558 | |||||||
| chr9:125269013 | A | T | 1 | a0001c0001t0002g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-150+29A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269013 | |||||||
| chr9:125269019 | A | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+35A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269019 | |||||||
| chr9:125269184 | C | T | 165 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(162): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-150+200C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269184 | |||||||
| chr9:125269259 | G | A | 1 | a0001c0001t0032g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-150+275G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269259 | |||||||
| chr9:125269418 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-150+434A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269418 | |||||||
| chr9:125269544 | C | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-150+560C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269544 | |||||||
| chr9:125269557 | A | G | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+573A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269557 | |||||||
| chr9:125269584 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-150+600C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269584 | |||||||
| chr9:125269710 | C | CT | 56 | a0001c0001t0001g0018 a0001c0001t0001g0177 a0001c0001t0001g0244 others(53): Show |
56 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-150+750dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125269710 | ||||||
| chr9:125269710 | CT | C | 24 | a0001c0001t0002g0017 a0001c0001t0002g0087 a0001c0001t0004g0007 others(21): Show |
24 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-150+750delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125269710 | ||||||
| chr9:125269710 | CTTTTTTT | C | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+744_-150+750d others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125269710 | ||||||
| chr9:125269831 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-150+847C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269831 | |||||||
| chr9:125269907 | C | T | 165 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(162): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-150+923C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269907 | |||||||
| chr9:125269947 | A | G | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-150+963A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269947 | |||||||
| chr9:125270284 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0268 a0001c0001t0001g0297 others(1): Show |
4 | HG00639.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-150+1300C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270284 | |||||||
| chr9:125270298 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0073 |
2 | HG02071.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-150+1314G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270298 | |||||||
| chr9:125270365 | T | G | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-150+1381T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270365 | |||||||
| chr9:125270544 | A | G | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+1560A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270544 | |||||||
| chr9:125270665 | C | T | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+1681C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270665 | |||||||
| chr9:125270791 | A | C | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-150+1807A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270791 | |||||||
| chr9:125270808 | T | A | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+1824T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270808 | |||||||
| chr9:125270873 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-150+1889T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270873 | |||||||
| chr9:125270903 | C | G | 1 | a0001c0001t0002g0114 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+1919C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270903 | |||||||
| chr9:125271138 | A | G | 13 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(10): Show |
13 | HG00558.hp1 HG02027.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-150+2154A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271138 | |||||||
| chr9:125271414 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-150+2430A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271414 | |||||||
| chr9:125271531 | G | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+2547G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271531 | |||||||
| chr9:125271676 | G | A | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-150+2692G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271676 | |||||||
| chr9:125271801 | T | G | 61 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(58): Show |
61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-150+2817T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271801 | |||||||
| chr9:125271806 | T | G | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+2822T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271806 | |||||||
| chr9:125272188 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3204T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272188 | |||||||
| chr9:125272249 | C | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-150+3265C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272249 | |||||||
| chr9:125272257 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3273C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272257 | |||||||
| chr9:125272311 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-150+3327C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272311 | |||||||
| chr9:125272383 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3399A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272383 | |||||||
| chr9:125272436 | G | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0265 |
3 | NA18942.hp2 NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-150+3452G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272436 | |||||||
| chr9:125272448 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3464A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272448 | |||||||
| chr9:125272876 | T | G | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+3892T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272876 | |||||||
| chr9:125272882 | G | T | 1 | a0001c0002t0003g0164 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-150+3898G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272882 | |||||||
| chr9:125273062 | C | T | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-150+4078C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273062 | |||||||
| chr9:125273170 | C | A | 162 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(159): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-150+4186C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273170 | |||||||
| chr9:125273278 | G | T | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+4294G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273278 | |||||||
| chr9:125273367 | C | A | 4 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0146 others(1): Show |
4 | NA18979.hp2 NA18988.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.-150+4383C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273367 | |||||||
| chr9:125273471 | G | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0240 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-150+4487G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273471 | |||||||
| chr9:125273501 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-150+4517T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273501 | |||||||
| chr9:125273511 | T | A | 1 | a0001c0001t0002g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-150+4527T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273511 | |||||||
| chr9:125273646 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+4662C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273646 | |||||||
| chr9:125273848 | G | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-150+4864G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273848 | |||||||
| chr9:125273934 | T | A | 8 | a0001c0001t0001g0200 a0001c0001t0001g0261 a0001c0001t0001g0323 others(5): Show |
8 | HG00738.hp1 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.-150+4950T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273934 | |||||||
| chr9:125274029 | C | T | 7 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+5045C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274029 | |||||||
| chr9:125274066 | G | A | 7 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+5082G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274066 | |||||||
| chr9:125274130 | G | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+5146G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274130 | |||||||
| chr9:125274215 | A | G | 1 | a0001c0001t0030g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-150+5231A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274215 | |||||||
| chr9:125274267 | C | T | 1 | a0001c0001t0014g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-150+5283C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274267 | |||||||
| chr9:125274312 | T | C | 199 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-150+5328T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274312 | |||||||
| chr9:125274355 | A | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+5371A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274355 | |||||||
| chr9:125274404 | G | A | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-150+5420G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274404 | |||||||
| chr9:125274430 | A | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+5446A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274430 | |||||||
| chr9:125274455 | G | A | 7 | a0001c0001t0001g0198 a0001c0001t0013g0196 a0001c0003t0004g0020 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+5471G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274455 | |||||||
| chr9:125274463 | CT | C | 6 | a0001c0001t0001g0261 a0001c0001t0002g0090 a0001c0001t0002g0120 others(3): Show |
6 | HG01167.hp2 HG02630.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+5496delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125274463 | ||||||
| chr9:125274497 | C | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+5513C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274497 | |||||||
| chr9:125274523 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-150+5539G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274523 | |||||||
| chr9:125274614 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-150+5630C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274614 | |||||||
| chr9:125274722 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-150+5738A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274722 | |||||||
| chr9:125274832 | A | G | 23 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0009g0002 others(20): Show |
23 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-150+5848A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274832 | |||||||
| chr9:125274966 | C | T | 196 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(193): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-150+5982C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274966 | |||||||
| chr9:125274974 | T | C | 1 | a0001c0001t0002g0032 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-150+5990T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274974 | |||||||
| chr9:125275062 | T | C | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-150+6078T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275062 | |||||||
| chr9:125275073 | A | C | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+6089A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275073 | |||||||
| chr9:125275096 | T | G | 2 | a0001c0001t0002g0092 a0001c0001t0002g0112 |
2 | HG02135.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-150+6112T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275096 | |||||||
| chr9:125275240 | T | A | 1 | a0001c0001t0008g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-150+6256T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275240 | |||||||
| chr9:125275264 | C | T | 1 | a0001c0001t0002g0031 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-150+6280C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275264 | |||||||
| chr9:125275266 | G | A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-150+6282G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275266 | |||||||
| chr9:125275550 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+6566G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275550 | |||||||
| chr9:125275597 | G | A | 1 | a0001c0001t0025g0205 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-150+6613G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275597 | |||||||
| chr9:125275729 | C | T | 2 | a0001c0002t0003g0163 a0001c0002t0003g0167 |
2 | HG00621.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-150+6745C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275729 | |||||||
| chr9:125275747 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+6763C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275747 | |||||||
| chr9:125275927 | G | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0311 |
2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-150+6943G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275927 | |||||||
| chr9:125276094 | C | T | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+7110C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276094 | |||||||
| chr9:125276143 | A | G | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+7159A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276143 | |||||||
| chr9:125276174 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-150+7190C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276174 | |||||||
| chr9:125276181 | A | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+7197A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276181 | |||||||
| chr9:125276216 | A | G | 20 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0003t0004g0020 others(17): Show |
20 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-150+7232A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276216 | |||||||
| chr9:125276273 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-150+7289T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276273 | |||||||
| chr9:125276380 | A | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0264 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-150+7396A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276380 | |||||||
| chr9:125276573 | C | A | 1 | a0001c0001t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-150+7589C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276573 | |||||||
| chr9:125276574 | A | G | 1 | a0001c0001t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-150+7590A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276574 | |||||||
| chr9:125276623 | A | T | 1 | a0001c0001t0002g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-150+7639A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276623 | |||||||
| chr9:125276638 | G | A | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+7654G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276638 | |||||||
| chr9:125276683 | T | C | 1 | a0001c0001t0002g0033 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-150+7699T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276683 | |||||||
| chr9:125276704 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-150+7720A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276704 | |||||||
| chr9:125276998 | T | C | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+8014T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276998 | |||||||
| chr9:125277243 | C | T | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+8259C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277243 | |||||||
| chr9:125277372 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-150+8388A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277372 | |||||||
| chr9:125277685 | G | GT | 19 | a0001c0001t0001g0204 a0001c0001t0001g0235 a0001c0001t0001g0236 others(16): Show |
19 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-150+8717dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125277685 | ||||||
| chr9:125277928 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0298 |
3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-150+8944G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277928 | |||||||
| chr9:125277971 | T | C | 4 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG01175.hp1 HG01192.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-150+8987T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277971 | |||||||
| chr9:125278049 | A | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+9065A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278049 | |||||||
| chr9:125278254 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-150+9270C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278254 | |||||||
| chr9:125278385 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-150+9401G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278385 | |||||||
| chr9:125278501 | A | T | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+9517A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278501 | |||||||
| chr9:125278574 | C | G | 1 | a0001c0001t0002g0114 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+9590C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278574 | |||||||
| chr9:125278750 | G | T | 162 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(159): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-150+9766G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278750 | |||||||
| chr9:125278835 | GA | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-150+9862delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125278835 | ||||||
| chr9:125278835 | GAA | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+9861_-150+986 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125278835 | ||||||
| chr9:125278982 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+9998A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278982 | |||||||
| chr9:125278983 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+9999G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278983 | |||||||
| chr9:125279209 | TA | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+10241delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125279209 | ||||||
| chr9:125279549 | C | T | 72 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0195 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-150+10565C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279549 | |||||||
| chr9:125279570 | CA | C | 61 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(58): Show |
61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-150+10603delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125279570 | ||||||
| chr9:125279637 | T | TA | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+10662dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125279637 | ||||||
| chr9:125279656 | C | A | 1 | a0001c0001t0002g0114 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+10672C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279656 | |||||||
| chr9:125279670 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-150+10686C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279670 | |||||||
| chr9:125279974 | CT | C | 7 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+10991delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279974 | |||||||
| chr9:125280014 | C | T | 7 | a0001c0001t0002g0092 a0001c0001t0002g0107 a0001c0001t0002g0108 others(4): Show |
7 | HG00408.hp2 HG02074.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+11030C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280014 | |||||||
| chr9:125280050 | G | A | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+11066G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280050 | |||||||
| chr9:125280264 | T | C | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+11280T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280264 | |||||||
| chr9:125280396 | C | CA | 11 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0028 others(8): Show |
11 | HG00733.hp2 HG01175.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.-150+11436dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280396 | ||||||
| chr9:125280396 | CA | C | 185 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(182): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-150+11436delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280396 | ||||||
| chr9:125280396 | CAA | C | 34 | a0001c0001t0001g0191 a0001c0001t0001g0234 a0001c0001t0001g0237 others(31): Show |
34 | HG00423.hp2 HG01099.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-150+11435_-150+11 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280396 | ||||||
| chr9:125280575 | C | CT | 12 | a0001c0001t0001g0239 a0001c0001t0001g0251 a0001c0001t0001g0292 others(9): Show |
12 | HG00408.hp1 HG00544.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-150+11609dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280575 | ||||||
| chr9:125280575 | CT | C | 10 | a0001c0001t0001g0211 a0001c0001t0001g0234 a0001c0001t0002g0114 others(7): Show |
10 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-150+11609delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280575 | ||||||
| chr9:125280661 | C | T | 162 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(159): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-150+11677C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280661 | |||||||
| chr9:125280779 | GT | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+11797delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280779 | ||||||
| chr9:125280797 | A | G | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-150+11813A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280797 | |||||||
| chr9:125280952 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-150+11968A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280952 | |||||||
| chr9:125280987 | G | A | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-150+12003G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280987 | |||||||
| chr9:125281525 | T | G | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-150+12541T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281525 | |||||||
| chr9:125281581 | G | C | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+12597G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281581 | |||||||
| chr9:125281908 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-150+12924C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281908 | |||||||
| chr9:125281986 | A | G | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-150+13002A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281986 | |||||||
| chr9:125282163 | C | G | 1 | a0001c0002t0007g0161 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-150+13179C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282163 | |||||||
| chr9:125282435 | C | T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-149-13023C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282435 | |||||||
| chr9:125282589 | T | G | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-12869T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282589 | |||||||
| chr9:125282595 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-149-12863A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282595 | |||||||
| chr9:125283020 | A | G | 4 | a0001c0001t0001g0326 a0001c0001t0005g0330 a0001c0001t0005g0331 others(1): Show |
4 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-12438A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283020 | |||||||
| chr9:125283028 | T | TTTTA | 84 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(81): Show |
84 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-149-12388_-149-12 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | ||||||
| chr9:125283028 | T | TTTTATTT others(1): Show |
40 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(37): Show |
40 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-149-12392_-149-12 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | ||||||
| chr9:125283028 | T | TTTTATTT others(5): Show |
8 | a0001c0001t0001g0208 a0001c0001t0001g0279 a0001c0001t0001g0315 others(5): Show |
8 | HG01257.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-12396_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | ||||||
| chr9:125283028 | T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-149-12427_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | ||||||
| chr9:125283028 | TTTTA | T | 7 | a0001c0001t0001g0251 a0001c0001t0002g0030 a0001c0002t0003g0005 others(4): Show |
7 | HG02056.hp2 HG02572.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-12388_-149-12 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | ||||||
| chr9:125283028 | TTTTATTT others(1): Show |
T | 5 | a0001c0001t0001g0326 a0001c0001t0005g0330 a0001c0001t0005g0331 others(2): Show |
5 | HG02129.hp1 HG02630.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149-12392_-149-12 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | ||||||
| chr9:125283028 | TTTTATTT others(5): Show |
T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0215 others(2): Show |
5 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-12396_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | ||||||
| chr9:125283070 | T | TTATTTAT others(5): Show |
1 | a0001c0001t0009g0004 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-149-12385_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283070 | ||||||
| chr9:125283141 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-12317C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283141 | |||||||
| chr9:125283310 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-149-12148C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283310 | |||||||
| chr9:125283386 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-12072G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283386 | |||||||
| chr9:125283449 | C | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-12009C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283449 | |||||||
| chr9:125283452 | C | T | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-12006C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283452 | |||||||
| chr9:125283455 | C | T | 1 | a0001c0001t0002g0024 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-149-12003C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283455 | |||||||
| chr9:125283787 | C | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-11671C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283787 | |||||||
| chr9:125283872 | C | CT | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-11576dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283872 | ||||||
| chr9:125283882 | T | C | 15 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(12): Show |
15 | HG00609.hp2 HG00673.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-149-11576T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283882 | |||||||
| chr9:125283954 | C | G | 5 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(2): Show |
5 | HG00544.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-11504C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283954 | |||||||
| chr9:125283989 | C | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-11469C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283989 | |||||||
| chr9:125283990 | A | T | 1 | a0001c0001t0002g0024 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-149-11468A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283990 | |||||||
| chr9:125284112 | G | C | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-11346G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284112 | |||||||
| chr9:125284164 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-149-11294C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284164 | |||||||
| chr9:125284168 | G | A | 1 | a0001c0002t0003g0170 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-149-11290G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284168 | |||||||
| chr9:125284180 | C | CT | 167 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(164): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-149-11257dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284180 | ||||||
| chr9:125284180 | C | CTT | 10 | a0001c0001t0001g0229 a0001c0001t0001g0268 a0001c0001t0001g0288 others(7): Show |
10 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-149-11258_-149-11 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284180 | ||||||
| chr9:125284180 | CT | C | 34 | a0001c0001t0002g0072 a0001c0001t0002g0087 a0001c0002t0003g0005 others(31): Show |
34 | HG00544.hp2 HG01081.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-149-11257delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284180 | ||||||
| chr9:125284247 | C | T | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-11211C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284247 | |||||||
| chr9:125284317 | T | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0252 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-149-11141T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284317 | |||||||
| chr9:125284337 | C | T | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149-11121C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284337 | |||||||
| chr9:125284380 | A | G | 2 | a0001c0001t0002g0090 a0001c0001t0002g0116 |
2 | HG02165.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-149-11078A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284380 | |||||||
| chr9:125284437 | C | G | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-11021C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284437 | |||||||
| chr9:125284479 | CT | C | 7 | a0001c0001t0002g0114 a0001c0003t0006g0132 a0001c0003t0006g0134 others(4): Show |
7 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-10966delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284479 | ||||||
| chr9:125284509 | G | A | 4 | a0001c0001t0001g0314 a0001c0001t0010g0213 a0001c0001t0010g0253 others(1): Show |
4 | HG00673.hp2 HG01175.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-10949G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284509 | |||||||
| chr9:125284512 | A | G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0002g0055 others(8): Show |
11 | HG00280.hp2 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.-149-10946A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284512 | |||||||
| chr9:125284567 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-149-10891C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284567 | |||||||
| chr9:125284707 | T | C | 1 | a0003c0007t0001g0300 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-149-10751T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284707 | |||||||
| chr9:125285005 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-10453G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285005 | |||||||
| chr9:125285007 | A | G | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-149-10451A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285007 | |||||||
| chr9:125285015 | T | G | 1 | a0001c0001t0002g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-149-10443T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285015 | |||||||
| chr9:125285056 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-10402C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285056 | |||||||
| chr9:125285224 | T | G | 1 | a0001c0001t0002g0140 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-149-10234T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285224 | |||||||
| chr9:125285306 | A | G | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-149-10152A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285306 | |||||||
| chr9:125285372 | G | C | 1 | a0001c0001t0002g0069 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-149-10086G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285372 | |||||||
| chr9:125285453 | G | GT | 162 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(159): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-149-9983dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125285453 | ||||||
| chr9:125285453 | G | GTT | 29 | a0001c0001t0001g0187 a0001c0001t0001g0226 a0001c0001t0001g0227 others(26): Show |
29 | HG00438.hp1 HG00609.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-149-9984_-149-998 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125285453 | ||||||
| chr9:125285453 | G | GTTT | 29 | a0001c0001t0004g0012 a0001c0001t0030g0141 a0001c0002t0003g0005 others(26): Show |
29 | HG00544.hp2 HG01069.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-149-9985_-149-998 others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125285453 | ||||||
| chr9:125285532 | C | A | 1 | a0001c0001t0002g0092 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-149-9926C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285532 | |||||||
| chr9:125285807 | T | C | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-149-9651T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285807 | |||||||
| chr9:125285840 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-149-9618A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285840 | |||||||
| chr9:125286180 | T | G | 1 | a0001c0003t0006g0132 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-149-9278T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286180 | |||||||
| chr9:125286196 | G | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-9262G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286196 | |||||||
| chr9:125286262 | C | T | 1 | a0001c0001t0004g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-149-9196C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286262 | |||||||
| chr9:125286294 | GTTGTTTT others(2): Show |
G | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-9156_-149-914 others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286294 | ||||||
| chr9:125286298 | TTTTC | T | 12 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-149-9156_-149-915 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286298 | ||||||
| chr9:125286311 | T | G | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-9147T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286311 | |||||||
| chr9:125286475 | G | GT | 13 | a0001c0001t0002g0068 a0001c0001t0002g0083 a0001c0001t0002g0085 others(10): Show |
13 | HG00423.hp1 HG01069.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-149-8971dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286475 | ||||||
| chr9:125286791 | A | ATTTTCTT others(10): Show |
1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-149-8666_-149-866 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286791 | ||||||
| chr9:125286809 | C | T | 1 | a0001c0001t0002g0017 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-149-8649C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286809 | |||||||
| chr9:125286874 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-149-8584A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286874 | |||||||
| chr9:125286900 | G | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-8558G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286900 | |||||||
| chr9:125286987 | G | A | 1 | a0001c0001t0005g0330 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-149-8471G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286987 | |||||||
| chr9:125287224 | A | G | 2 | a0001c0002t0003g0159 a0001c0002t0003g0170 |
2 | NA18986.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-149-8234A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287224 | |||||||
| chr9:125287225 | G | A | 2 | a0001c0002t0003g0159 a0001c0002t0003g0170 |
2 | NA18986.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-149-8233G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287225 | |||||||
| chr9:125287324 | G | A | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-8134G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287324 | |||||||
| chr9:125287765 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-7693G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287765 | |||||||
| chr9:125287841 | A | G | 1 | a0001c0001t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-149-7617A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287841 | |||||||
| chr9:125287970 | C | T | 2 | a0001c0001t0001g0259 a0005c0017t0001g0249 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-149-7488C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287970 | |||||||
| chr9:125288112 | A | AT | 10 | a0001c0001t0001g0275 a0001c0001t0001g0295 a0001c0001t0001g0296 others(7): Show |
10 | HG01123.hp2 HG02258.hp2 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.-149-7329dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125288112 | ||||||
| chr9:125288326 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-149-7132G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288326 | |||||||
| chr9:125288327 | G | A | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-149-7131G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288327 | |||||||
| chr9:125288503 | G | A | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-149-6955G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288503 | |||||||
| chr9:125288690 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-149-6768A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288690 | |||||||
| chr9:125288887 | G | A | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-149-6571G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288887 | |||||||
| chr9:125288930 | A | G | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG01069.hp1 HG02135.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-149-6528A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288930 | |||||||
| chr9:125289158 | A | G | 1 | a0001c0010t0006g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-6300A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289158 | |||||||
| chr9:125289362 | GT | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-6094delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125289362 | ||||||
| chr9:125289408 | G | A | 7 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-6050G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289408 | |||||||
| chr9:125289795 | A | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-5663A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289795 | |||||||
| chr9:125289861 | A | G | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-5597A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289861 | |||||||
| chr9:125289925 | G | A | 1 | a0001c0001t0034g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-149-5533G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289925 | |||||||
| chr9:125290008 | A | T | 1 | a0001c0001t0002g0027 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-149-5450A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290008 | |||||||
| chr9:125290165 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-149-5293C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290165 | |||||||
| chr9:125290273 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-5185G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290273 | |||||||
| chr9:125290353 | A | G | 21 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(18): Show |
21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-149-5105A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290353 | |||||||
| chr9:125290409 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-149-5049T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290409 | |||||||
| chr9:125290419 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-5039A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290419 | |||||||
| chr9:125290423 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-149-5035G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290423 | |||||||
| chr9:125290449 | A | G | 21 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(18): Show |
21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-149-5009A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290449 | |||||||
| chr9:125290502 | G | A | 17 | a0001c0001t0002g0024 a0001c0001t0002g0089 a0001c0001t0002g0090 others(14): Show |
17 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.-149-4956G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290502 | |||||||
| chr9:125290557 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0311 |
2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-149-4901C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290557 | |||||||
| chr9:125290661 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0292 |
2 | NA18974.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-149-4797G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290661 | |||||||
| chr9:125290686 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-4772G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290686 | |||||||
| chr9:125290723 | A | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0079 |
2 | NA18989.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-149-4735A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290723 | |||||||
| chr9:125290977 | A | G | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-149-4481A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290977 | |||||||
| chr9:125290994 | T | TA | 153 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(150): Show |
153 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-149-4446dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125290994 | ||||||
| chr9:125290994 | T | TAA | 8 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0271 others(5): Show |
8 | HG00733.hp1 HG02698.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-4447_-149-444 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125290994 | ||||||
| chr9:125291225 | G | A | 3 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 |
3 | HG01192.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-149-4233G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125291225 | |||||||
| chr9:125291450 | G | A | 3 | a0001c0001t0001g0238 a0001c0001t0001g0264 a0001c0003t0006g0123 |
3 | HG01884.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-149-4008G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125291450 | |||||||
| chr9:125291709 | G | GACCCATA others(10): Show |
1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-3748_-149-373 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125291709 | ||||||
| chr9:125291970 | G | C | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-3488G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125291970 | |||||||
| chr9:125292033 | A | G | 1 | a0007c0015t0002g0049 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-149-3425A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292033 | |||||||
| chr9:125292046 | T | G | 3 | a0001c0001t0002g0090 a0001c0001t0002g0116 a0001c0001t0028g0113 |
3 | HG02165.hp2 NA18967.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-149-3412T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292046 | |||||||
| chr9:125292117 | A | C | 336 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-149-3341A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292117 | |||||||
| chr9:125292130 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-3328G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292130 | |||||||
| chr9:125292136 | C | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-3322C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292136 | |||||||
| chr9:125292206 | C | T | 3 | a0001c0001t0001g0297 a0001c0002t0007g0162 a0001c0002t0007g0168 |
3 | HG02970.hp2 NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-149-3252C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292206 | |||||||
| chr9:125292270 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-3188A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292270 | |||||||
| chr9:125292400 | A | AT | 9 | a0001c0001t0002g0119 a0001c0003t0006g0123 a0001c0003t0006g0124 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-149-3045dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125292400 | ||||||
| chr9:125292527 | G | A | 1 | a0001c0001t0002g0017 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-149-2931G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292527 | |||||||
| chr9:125292544 | C | G | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-2914C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292544 | |||||||
| chr9:125292688 | C | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-2770C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292688 | |||||||
| chr9:125292813 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-2645T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292813 | |||||||
| chr9:125293015 | G | T | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-2443G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293015 | |||||||
| chr9:125293178 | A | G | 199 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-149-2280A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293178 | |||||||
| chr9:125293543 | G | A | 1 | a0001c0001t0015g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-149-1915G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293543 | |||||||
| chr9:125293611 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-1847A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293611 | |||||||
| chr9:125293618 | T | TTTATATA others(32): Show |
61 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(58): Show |
61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-149-1829_-149-179 others(43): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293618 | T | TTTATATA others(61): Show |
1 | a0001c0001t0001g0325 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-149-1800_-149-179 others(72): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293618 | T | TTTATATA others(60): Show |
1 | a0001c0001t0001g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-149-1831_-149-176 others(71): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293618 | T | TTTATATA others(62): Show |
88 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0195 others(85): Show |
88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(73): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293618 | T | TTTATATA others(92): Show |
3 | a0001c0001t0001g0191 a0001c0001t0001g0215 a0001c0001t0001g0228 |
3 | HG03041.hp1 HG03831.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(103): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293618 | T | TTTATATA others(71): Show |
1 | a0001c0001t0001g0286 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-149-1791_-149-179 others(82): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293618 | T | TTTATATA others(59): Show |
1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1810_-149-180 others(70): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293618 | T | TTTATATA others(63): Show |
1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-1829_-149-182 others(74): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | ||||||
| chr9:125293629 | T | TATATATA others(21): Show |
1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-1828_-149-180 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293629 | ||||||
| chr9:125293630 | A | ATATATAT others(21): Show |
1 | a0001c0001t0016g0053 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-149-1792_-149-176 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | ||||||
| chr9:125293630 | A | ATATATAT others(30): Show |
2 | a0001c0001t0002g0308 a0001c0001t0002g0313 |
2 | NA18939.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-149-1827_-149-179 others(41): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | ||||||
| chr9:125293630 | A | ATATATAT others(88): Show |
2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-1785_-149-178 others(99): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | ||||||
| chr9:125293630 | A | ATATATAT others(60): Show |
3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0297 |
3 | HG02280.hp1 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(71): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | ||||||
| chr9:125293630 | ATATATAT others(21): Show |
A | 2 | a0001c0003t0006g0125 a0001c0016t0037g0171 |
2 | HG02280.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-149-1792_-149-176 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | ||||||
| chr9:125293650 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0052 |
2 | HG01099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-149-1808T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293650 | |||||||
| chr9:125293658 | T | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-1800T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293658 | |||||||
| chr9:125293658 | T | TTA | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-1791_-149-179 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293658 | ||||||
| chr9:125293658 | T | TTATATAT others(34): Show |
2 | a0001c0001t0001g0223 a0001c0001t0002g0256 |
2 | HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(45): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293658 | ||||||
| chr9:125293660 | A | ATATATAT others(30): Show |
1 | a0001c0001t0002g0310 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-149-1791_-149-179 others(41): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293660 | ||||||
| chr9:125293663 | TATATA | T | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1788_-149-178 others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293663 | ||||||
| chr9:125293676 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-149-1782A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293676 | |||||||
| chr9:125293709 | AT | A | 32 | a0001c0001t0001g0229 a0001c0001t0002g0015 a0001c0001t0002g0016 others(29): Show |
32 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-149-1744delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293709 | ||||||
| chr9:125293723 | T | G | 103 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.-149-1735T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293723 | |||||||
| chr9:125293770 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1688T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293770 | |||||||
| chr9:125293771 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1687A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293771 | |||||||
| chr9:125293784 | A | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0268 a0001c0001t0001g0322 |
3 | HG00639.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-149-1674A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293784 | |||||||
| chr9:125293798 | A | C | 89 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0195 others(86): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-149-1660A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293798 | |||||||
| chr9:125293818 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-1640G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293818 | |||||||
| chr9:125293824 | TA | T | 4 | a0001c0001t0002g0051 a0001c0001t0002g0061 a0001c0001t0002g0066 others(1): Show |
4 | HG00733.hp2 HG00741.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1627delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293824 | ||||||
| chr9:125293830 | A | T | 3 | a0001c0001t0001g0184 a0001c0001t0004g0172 a0001c0001t0004g0173 |
3 | HG01099.hp1 HG02257.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-149-1628A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293830 | |||||||
| chr9:125293832 | T | A | 1 | a0001c0001t0015g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-149-1626T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293832 | |||||||
| chr9:125293840 | T | A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0068 |
2 | HG03831.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-149-1618T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293840 | |||||||
| chr9:125293840 | TA | T | 6 | a0001c0001t0001g0290 a0001c0003t0006g0127 a0001c0003t0006g0135 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-1613delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293840 | ||||||
| chr9:125293842 | A | AAAATATA others(14): Show |
5 | a0001c0001t0001g0279 a0001c0001t0001g0309 a0001c0001t0005g0306 others(2): Show |
5 | HG02056.hp1 HG04184.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-1614_-149-159 others(25): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293842 | ||||||
| chr9:125293842 | A | AAAATATA others(35): Show |
2 | a0001c0001t0001g0275 a0001c0001t0001g0316 |
2 | NA18953.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(46): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293842 | ||||||
| chr9:125293842 | A | AAATATAT others(11): Show |
2 | a0001c0003t0006g0132 a0001c0003t0006g0134 |
2 | HG01167.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-149-1614_-149-161 others(22): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293842 | ||||||
| chr9:125293842 | A | T | 10 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(7): Show |
10 | HG01069.hp1 HG01099.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-149-1616A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293842 | |||||||
| chr9:125293844 | A | ATATATTA others(55): Show |
2 | a0001c0002t0003g0005 a0001c0002t0003g0006 |
2 | NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1614_-149-161 others(66): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293844 | |||||||
| chr9:125293844 | A | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0068 |
2 | HG03831.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-149-1614A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293844 | |||||||
| chr9:125293849 | A | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0068 |
2 | HG03831.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-149-1609A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293849 | |||||||
| chr9:125293850 | TTTTATAT others(25): Show |
T | 1 | a0001c0001t0002g0035 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-149-1606_-149-157 others(36): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293850 | ||||||
| chr9:125293851 | T | A | 2 | a0001c0002t0003g0005 a0001c0002t0003g0006 |
2 | NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1607T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293851 | |||||||
| chr9:125293851 | TTTATATA others(6): Show |
T | 1 | a0001c0001t0002g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-149-1605_-149-159 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293851 | ||||||
| chr9:125293852 | T | A | 35 | a0001c0001t0001g0239 a0001c0001t0002g0026 a0001c0001t0002g0068 others(32): Show |
35 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-149-1606T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293852 | |||||||
| chr9:125293852 | T | TTA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0002g0024 others(7): Show |
10 | HG00544.hp1 HG01099.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-149-1555_-149-155 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATA | 7 | a0001c0001t0002g0025 a0001c0001t0002g0097 a0001c0001t0002g0104 others(4): Show |
7 | HG00408.hp2 HG01167.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1557_-149-155 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATA | 6 | a0001c0001t0002g0078 a0001c0001t0002g0081 a0001c0001t0002g0082 others(3): Show |
6 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-1559_-149-155 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(1): Show |
4 | a0001c0001t0002g0106 a0001c0001t0002g0110 a0001c0001t0028g0113 others(1): Show |
4 | NA18959.hp2 NA18967.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1561_-149-155 others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(3): Show |
4 | a0001c0001t0002g0116 a0001c0001t0002g0119 a0001c0001t0002g0140 others(1): Show |
4 | HG00738.hp2 HG02165.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149-1563_-149-155 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(20): Show |
2 | a0001c0003t0006g0135 a0001c0003t0006g0138 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-149-1596_-149-159 others(31): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(22): Show |
1 | a0001c0003t0006g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(33): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(41): Show |
1 | a0001c0003t0026g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(52): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(20): Show |
1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(31): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(7): Show |
3 | a0001c0001t0002g0028 a0001c0001t0002g0062 a0001c0001t0002g0071 |
3 | HG03688.hp2 NA18978.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-149-1567_-149-155 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(11): Show |
3 | a0001c0001t0002g0069 a0001c0001t0002g0089 a0001c0001t0015g0063 |
3 | HG00099.hp2 HG00438.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-149-1571_-149-155 others(22): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | T | TTATATAT others(13): Show |
1 | a0001c0001t0002g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-149-1573_-149-155 others(24): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTA | T | 11 | a0001c0001t0002g0015 a0001c0001t0002g0044 a0001c0001t0002g0045 others(8): Show |
11 | HG02074.hp2 HG02165.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-149-1555_-149-155 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATA | T | 14 | a0001c0001t0002g0023 a0001c0001t0002g0029 a0001c0001t0002g0030 others(11): Show |
14 | HG00280.hp2 HG00673.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-149-1557_-149-155 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATA | T | 8 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0031 others(5): Show |
8 | HG00733.hp2 HG02071.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-1559_-149-155 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(1): Show |
T | 7 | a0001c0001t0002g0033 a0001c0001t0002g0040 a0001c0001t0002g0058 others(4): Show |
7 | HG01192.hp1 HG01192.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1561_-149-155 others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(3): Show |
T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0100 |
2 | HG03704.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-149-1563_-149-155 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0002g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-149-1565_-149-155 others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(7): Show |
T | 1 | a0001c0004t0001g0038 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-149-1567_-149-155 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(9): Show |
T | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-149-1569_-149-155 others(20): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(23): Show |
T | 1 | a0001c0001t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-149-1583_-149-155 others(34): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(25): Show |
T | 1 | a0001c0001t0030g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-149-1585_-149-155 others(36): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293852 | TTATATAT others(31): Show |
T | 1 | a0001c0001t0002g0032 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-149-1591_-149-155 others(42): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | ||||||
| chr9:125293854 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | ||||||
| chr9:125293854 | A | ATATATAT others(10): Show |
1 | a0001c0010t0006g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | ||||||
| chr9:125293854 | A | ATATATAT others(37): Show |
1 | a0001c0003t0006g0128 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(48): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | ||||||
| chr9:125293854 | A | ATATATAT others(12): Show |
6 | a0001c0001t0001g0284 a0001c0001t0001g0302 a0001c0001t0001g0303 others(3): Show |
6 | HG02300.hp2 NA18942.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(23): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | ||||||
| chr9:125293854 | A | ATATATAT others(33): Show |
4 | a0001c0001t0001g0270 a0001c0001t0001g0292 a0001c0001t0001g0314 others(1): Show |
4 | HG00673.hp2 NA18952.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(44): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | ||||||
| chr9:125293854 | A | T | 1 | a0001c0001t0002g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-149-1604A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293854 | |||||||
| chr9:125293856 | A | ATATATAA others(6): Show |
1 | a0001c0001t0004g0173 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293856 | ||||||
| chr9:125293856 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0183 a0001c0001t0001g0187 |
2 | HG00558.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293856 | ||||||
| chr9:125293858 | A | ATATATAA others(8): Show |
11 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0185 others(8): Show |
11 | HG00621.hp2 HG02004.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293858 | ||||||
| chr9:125293858 | A | ATATATAA others(29): Show |
4 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0291 others(1): Show |
4 | HG01255.hp1 NA18985.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(40): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293858 | ||||||
| chr9:125293860 | A | AAATATAA others(55): Show |
28 | a0001c0002t0003g0144 a0001c0002t0003g0146 a0001c0002t0003g0149 others(25): Show |
28 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.-149-1598_-149-159 others(66): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293860 | |||||||
| chr9:125293860 | A | AAATATAA others(53): Show |
1 | a0001c0002t0003g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-149-1598_-149-159 others(64): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293860 | |||||||
| chr9:125293860 | A | ATATAAAT others(6): Show |
6 | a0001c0001t0001g0272 a0001c0001t0001g0281 a0001c0001t0001g0286 others(3): Show |
6 | HG00438.hp1 HG01243.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293860 | ||||||
| chr9:125293860 | A | ATATAAAT others(27): Show |
4 | a0001c0001t0001g0269 a0001c0001t0001g0273 a0001c0001t0001g0277 others(1): Show |
4 | HG00609.hp2 NA18974.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(38): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293860 | ||||||
| chr9:125293862 | A | ATAAATAT others(4): Show |
7 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0287 others(4): Show |
7 | HG03688.hp1 HG03704.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293862 | ||||||
| chr9:125293862 | A | ATATATAA others(6): Show |
1 | a0001c0003t0004g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-149-1590_-149-158 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293862 | ||||||
| chr9:125293863 | T | A | 8 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-149-1595T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293863 | |||||||
| chr9:125293864 | A | AAATATAT | 6 | a0001c0001t0001g0175 a0001c0001t0001g0181 a0001c0001t0001g0184 others(3): Show |
6 | HG03540.hp2 HG03710.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | |||||||
| chr9:125293864 | A | AAATATAT others(21): Show |
1 | a0001c0001t0001g0271 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | |||||||
| chr9:125293864 | A | AAATATAT others(39): Show |
1 | a0001c0001t0001g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(50): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | |||||||
| chr9:125293864 | A | AAATATAT others(39): Show |
1 | a0001c0001t0001g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(50): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | |||||||
| chr9:125293865 | T | A | 112 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(109): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-149-1593T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293865 | |||||||
| chr9:125293866 | A | AAAATATA others(26): Show |
2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-1592_-149-159 others(37): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293866 | |||||||
| chr9:125293866 | A | ATATTTTA others(75): Show |
1 | a0001c0003t0006g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(86): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293866 | ||||||
| chr9:125293866 | A | T | 8 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0181 others(5): Show |
8 | HG03540.hp2 HG03710.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-1592A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293866 | |||||||
| chr9:125293868 | A | AT | 29 | a0001c0002t0003g0144 a0001c0002t0003g0146 a0001c0002t0003g0147 others(26): Show |
29 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-149-1589dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | ||||||
| chr9:125293868 | A | ATTTTATA others(75): Show |
1 | a0001c0003t0006g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(86): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | ||||||
| chr9:125293868 | A | ATTTTATA others(127): Show |
1 | a0001c0003t0006g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(138): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | ||||||
| chr9:125293868 | A | ATTTTATA others(77): Show |
1 | a0001c0003t0006g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(88): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | ||||||
| chr9:125293870 | A | AT | 3 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 |
3 | HG02615.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-149-1587dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293870 | ||||||
| chr9:125293870 | A | ATTT | 3 | a0001c0001t0001g0289 a0001c0001t0004g0013 a0001c0001t0017g0014 |
3 | HG02630.hp1 HG02698.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-149-1587_-149-158 others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293870 | ||||||
| chr9:125293870 | A | ATTTTATA others(25): Show |
1 | a0001c0001t0004g0012 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-149-1587_-149-158 others(36): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293870 | ||||||
| chr9:125293871 | T | A | 3 | a0001c0003t0004g0021 a0001c0003t0004g0136 a0001c0003t0018g0131 |
3 | HG02258.hp1 HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-149-1587T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | |||||||
| chr9:125293871 | TA | T | 3 | a0001c0001t0001g0311 a0001c0001t0004g0007 a0001c0001t0004g0008 |
3 | HG02818.hp2 HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-149-1586delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | |||||||
| chr9:125293871 | TATATATA others(4): Show |
T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG00408.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1586_-149-157 others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | |||||||
| chr9:125293871 | TATATATA others(6): Show |
T | 96 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(93): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-149-1586_-149-157 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | |||||||
| chr9:125293871 | TATATATA others(8): Show |
T | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1586_-149-157 others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | |||||||
| chr9:125293872 | A | T | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1586A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293872 | |||||||
| chr9:125293874 | A | T | 5 | a0001c0001t0001g0311 a0001c0001t0004g0007 a0001c0001t0004g0008 others(2): Show |
5 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-1584A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293874 | |||||||
| chr9:125293875 | T | TA | 3 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0164 |
3 | NA18966.hp1 NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1582dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293875 | ||||||
| chr9:125293876 | A | T | 5 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0003t0006g0124 others(2): Show |
5 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-1582A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293876 | |||||||
| chr9:125293877 | T | TA | 28 | a0001c0002t0003g0144 a0001c0002t0003g0146 a0001c0002t0003g0147 others(25): Show |
28 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.-149-1580dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293877 | ||||||
| chr9:125293877 | T | TTATATAT others(9): Show |
2 | a0001c0003t0004g0021 a0001c0003t0018g0131 |
2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-149-1581_-149-158 others(20): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293877 | |||||||
| chr9:125293877 | T | TTATATAT others(13): Show |
1 | a0001c0003t0004g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-149-1581_-149-158 others(24): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293877 | |||||||
| chr9:125293878 | A | ATATATAA others(41): Show |
1 | a0001c0003t0006g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-149-1574_-149-157 others(52): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293878 | ||||||
| chr9:125293881 | T | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-1577T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293881 | |||||||
| chr9:125293884 | A | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG00408.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1574A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293884 | |||||||
| chr9:125293885 | TA | T | 3 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0164 |
3 | NA18966.hp1 NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1572delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293885 | |||||||
| chr9:125293886 | A | AT | 30 | a0001c0002t0003g0144 a0001c0002t0003g0146 a0001c0002t0003g0147 others(27): Show |
30 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.-149-1571dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293886 | ||||||
| chr9:125293886 | A | T | 92 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(89): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-149-1572A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293886 | |||||||
| chr9:125293888 | A | T | 3 | a0001c0001t0001g0229 a0002c0006t0011g0142 a0002c0006t0011g0143 |
3 | HG01109.hp2 HG03098.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-149-1570A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293888 | |||||||
| chr9:125293895 | T | G | 1 | a0001c0001t0002g0310 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-149-1563T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293895 | |||||||
| chr9:125293903 | T | A | 1 | a0001c0010t0006g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-1555T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293903 | |||||||
| chr9:125293940 | G | A | 1 | a0001c0003t0018g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-149-1518G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293940 | |||||||
| chr9:125293955 | C | A | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | NA18949.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-149-1503C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293955 | |||||||
| chr9:125294115 | T | C | 1 | a0001c0010t0006g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-1343T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294115 | |||||||
| chr9:125294149 | G | A | 8 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(5): Show |
8 | HG01069.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-1309G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294149 | |||||||
| chr9:125294287 | C | T | 1 | a0001c0003t0006g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-149-1171C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294287 | |||||||
| chr9:125294336 | C | T | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG02027.hp2 NA18943.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-1122C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294336 | |||||||
| chr9:125294348 | C | CT | 14 | a0001c0001t0001g0185 a0001c0001t0001g0230 a0001c0001t0001g0279 others(11): Show |
14 | HG02071.hp1 HG02683.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.-149-1093dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294348 | ||||||
| chr9:125294370 | C | T | 1 | a0001c0001t0008g0034 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-149-1088C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294370 | |||||||
| chr9:125294386 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-1072C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294386 | |||||||
| chr9:125294415 | C | T | 9 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(6): Show |
9 | HG00738.hp2 HG01069.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-149-1043C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294415 | |||||||
| chr9:125294474 | G | C | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-149-984G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294474 | |||||||
| chr9:125294503 | T | C | 1 | a0001c0001t0004g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-149-955T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294503 | |||||||
| chr9:125294507 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-149-951C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294507 | |||||||
| chr9:125294522 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-149-936T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294522 | |||||||
| chr9:125294636 | G | A | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-822G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294636 | |||||||
| chr9:125294652 | G | GT | 93 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0001t0001g0194 others(90): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-149-789dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294652 | ||||||
| chr9:125294652 | G | GTT | 11 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0001t0001g0230 others(8): Show |
11 | HG00738.hp1 HG02602.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.-149-790_-149-789d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294652 | ||||||
| chr9:125294652 | G | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-806G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294652 | |||||||
| chr9:125294652 | GT | G | 41 | a0001c0001t0002g0059 a0001c0001t0002g0061 a0001c0001t0002g0068 others(38): Show |
41 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-149-789delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294652 | ||||||
| chr9:125294667 | T | C | 1 | a0001c0002t0003g0159 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-149-791T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294667 | |||||||
| chr9:125294670 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-788C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294670 | |||||||
| chr9:125294671 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-787A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294671 | |||||||
| chr9:125294746 | T | G | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-712T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294746 | |||||||
| chr9:125294747 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-711G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294747 | |||||||
| chr9:125294908 | G | A | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-550G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294908 | |||||||
| chr9:125294930 | G | T | 1 | a0001c0004t0002g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-149-528G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294930 | |||||||
| chr9:125294962 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-496T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294962 | |||||||
| chr9:125295254 | T | C | 1 | a0001c0001t0005g0337 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-149-204T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295254 | |||||||
| chr9:125295354 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-104T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295354 | |||||||
| chr9:125295358 | A | C | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-100A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295358 | |||||||
| chr9:125295359 | T | G | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-99T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295359 | |||||||
| chr9:125295360 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-98T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295360 | |||||||
| chr9:125295361 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-97A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295361 | |||||||
| chr9:125295363 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-95A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295363 | |||||||
| chr9:125295364 | G | T | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-94G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295364 | |||||||
| chr9:125295429 | C | CT | 14 | a0001c0001t0002g0024 a0001c0001t0002g0027 a0001c0001t0002g0028 others(11): Show |
14 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.-149-8dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125295429 | ||||||
| chr9:125295429 | CT | C | 182 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(179): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
splice_region_variant&intron_variant | LOW | c.-149-8delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125295429 | ||||||
| chr9:125295429 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.-149-19_-149-8delT others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125295429 | ||||||
| chr9:125295643 | A | G | 165 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(162): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-33+69A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125295643 | |||||||
| chr9:125296098 | A | T | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-33+524A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296098 | |||||||
| chr9:125296108 | A | T | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33+534A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296108 | |||||||
| chr9:125296140 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-33+566T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296140 | |||||||
| chr9:125296271 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-33+697C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296271 | |||||||
| chr9:125296333 | A | C | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-33+759A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296333 | |||||||
| chr9:125296357 | G | GGTTTTTT others(5): Show |
3 | a0001c0002t0003g0160 a0002c0006t0011g0142 a0002c0006t0011g0143 |
3 | HG01109.hp2 HG03098.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.-33+784_-33+795dup others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296357 | ||||||
| chr9:125296358 | G | GTTTTTTT others(6): Show |
191 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(188): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-33+795_-33+796ins others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | ||||||
| chr9:125296358 | G | GTTTTTTT others(7): Show |
27 | a0001c0001t0001g0228 a0001c0001t0001g0234 a0001c0001t0001g0246 others(24): Show |
27 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-33+795_-33+796ins others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | ||||||
| chr9:125296358 | G | GTTTTTTT others(7): Show |
1 | a0001c0002t0003g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-33+796_-33+797ins others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | ||||||
| chr9:125296358 | G | GTTTTTTT others(6): Show |
7 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+787_-33+799dup others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | ||||||
| chr9:125296358 | G | GTTTTTTT others(7): Show |
1 | a0001c0003t0004g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-33+786_-33+799dup others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | ||||||
| chr9:125296390 | C | G | 1 | a0001c0001t0001g0320 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-33+816C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296390 | |||||||
| chr9:125296487 | T | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+913T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296487 | |||||||
| chr9:125296653 | C | CT | 32 | a0001c0001t0002g0043 a0001c0001t0004g0007 a0001c0001t0004g0008 others(29): Show |
32 | HG01069.hp1 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-33+1093dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296653 | ||||||
| chr9:125296653 | C | CTT | 34 | a0001c0001t0001g0271 a0001c0002t0003g0005 a0001c0002t0003g0006 others(31): Show |
34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+1092_-33+1093d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296653 | ||||||
| chr9:125296653 | C | CTTT | 162 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(159): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-33+1091_-33+1093d others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296653 | ||||||
| chr9:125296952 | G | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0286 |
2 | HG02071.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-33+1378G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296952 | |||||||
| chr9:125297199 | T | C | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33+1625T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297199 | |||||||
| chr9:125297612 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-32-1278G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297612 | |||||||
| chr9:125297714 | A | G | 1 | a0005c0017t0001g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-32-1176A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297714 | |||||||
| chr9:125297782 | A | G | 1 | a0001c0002t0003g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-32-1108A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297782 | |||||||
| chr9:125297798 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-32-1092T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297798 | |||||||
| chr9:125297894 | C | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0084 a0007c0015t0002g0049 |
3 | NA18941.hp1 NA18964.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-32-996C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297894 | |||||||
| chr9:125297966 | G | A | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-924G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297966 | |||||||
| chr9:125298035 | C | T | 1 | a0001c0002t0003g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-32-855C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298035 | |||||||
| chr9:125298041 | C | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0030 a0001c0001t0002g0033 others(5): Show |
8 | HG00673.hp1 HG02056.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32-849C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298041 | |||||||
| chr9:125298106 | G | A | 21 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(18): Show |
21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-32-784G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298106 | |||||||
| chr9:125298278 | G | T | 14 | a0001c0001t0001g0299 a0001c0001t0001g0302 a0001c0001t0001g0303 others(11): Show |
14 | HG02004.hp1 HG02056.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32-612G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298278 | |||||||
| chr9:125298290 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-32-600A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298290 | |||||||
| chr9:125298321 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-569C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298321 | |||||||
| chr9:125298432 | T | C | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-32-458T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298432 | |||||||
| chr9:125298481 | A | AT | 96 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0198 others(93): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.-32-383dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | ||||||
| chr9:125298481 | A | ATT | 59 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(56): Show |
59 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-32-384_-32-383dup others(2): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | ||||||
| chr9:125298481 | A | ATTT | 13 | a0001c0001t0001g0222 a0001c0001t0001g0251 a0001c0001t0001g0275 others(10): Show |
13 | HG02071.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-385_-32-383dup others(3): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | ||||||
| chr9:125298481 | AT | A | 45 | a0001c0001t0002g0061 a0001c0001t0002g0087 a0001c0001t0002g0122 others(42): Show |
45 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-32-383delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | ||||||
| chr9:125298481 | ATT | A | 9 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(6): Show |
9 | HG01167.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-384_-32-383del others(2): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | ||||||
| chr9:125298481 | ATTTTTT | A | 7 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(4): Show |
7 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-388_-32-383del others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | ||||||
| chr9:125298581 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-32-309C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298581 | |||||||
| chr9:125299114 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG00423.hp1 | splice_region_variant&intron_variant | LOW | c.185+8G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299114 | |||||||
| chr9:125299225 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+119A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299225 | |||||||
| chr9:125299330 | C | T | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.185+224C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299330 | |||||||
| chr9:125299370 | A | G | 1 | a0001c0001t0004g0011 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.185+264A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299370 | |||||||
| chr9:125299423 | C | T | 2 | a0001c0002t0003g0156 a0001c0002t0003g0158 |
2 | NA18940.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.185+317C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299423 | |||||||
| chr9:125299428 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+322C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299428 | |||||||
| chr9:125299429 | G | A | 1 | a0001c0001t0024g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.185+323G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299429 | |||||||
| chr9:125299666 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.185+560A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299666 | |||||||
| chr9:125299668 | A | G | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+562A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299668 | |||||||
| chr9:125299753 | G | T | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.185+647G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299753 | |||||||
| chr9:125299775 | C | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.185+669C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299775 | |||||||
| chr9:125299821 | C | G | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+715C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299821 | |||||||
| chr9:125299846 | C | G | 1 | a0001c0005t0001g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185+740C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299846 | |||||||
| chr9:125300023 | G | GAAAA | 6 | a0001c0001t0001g0202 a0001c0001t0001g0236 a0001c0001t0001g0271 others(3): Show |
6 | HG02723.hp1 HG02922.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+930_185+933dup others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAA | 8 | a0001c0001t0001g0181 a0001c0001t0001g0217 a0001c0001t0001g0235 others(5): Show |
8 | HG02970.hp1 HG03486.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+929_185+933dup others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAA | 13 | a0001c0001t0001g0195 a0001c0001t0001g0201 a0001c0001t0001g0210 others(10): Show |
13 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+928_185+933dup others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA | 10 | a0001c0001t0001g0184 a0001c0001t0001g0209 a0001c0001t0001g0220 others(7): Show |
10 | HG00140.hp2 HG00280.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+927_185+933dup others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(1): Show |
11 | a0001c0001t0001g0191 a0001c0001t0001g0245 a0001c0001t0001g0254 others(8): Show |
11 | HG02622.hp2 HG02717.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+926_185+933dup others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(2): Show |
13 | a0001c0001t0001g0178 a0001c0001t0001g0182 a0001c0001t0001g0183 others(10): Show |
13 | HG00558.hp1 HG01261.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+925_185+933dup others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(3): Show |
2 | a0001c0001t0001g0194 a0001c0001t0010g0253 |
2 | HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.185+924_185+933dup others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(4): Show |
8 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0186 others(5): Show |
8 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+923_185+933dup others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(5): Show |
10 | a0001c0001t0001g0180 a0001c0001t0001g0225 a0001c0001t0001g0232 others(7): Show |
10 | HG00099.hp1 HG00408.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+922_185+933dup others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(6): Show |
5 | a0001c0001t0001g0204 a0001c0001t0001g0222 a0001c0001t0001g0244 others(2): Show |
5 | HG02280.hp1 HG04204.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+921_185+933dup others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(7): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0251 a0001c0001t0010g0213 |
3 | HG01517.hp1 HG02572.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.185+920_185+933dup others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(8): Show |
6 | a0001c0001t0001g0223 a0001c0001t0001g0265 a0001c0001t0001g0326 others(3): Show |
6 | HG01993.hp1 NA18747.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+919_185+933dup others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(9): Show |
3 | a0001c0001t0005g0329 a0001c0001t0005g0331 a0001c0005t0001g0216 |
3 | HG02004.hp2 NA18950.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.185+918_185+933dup others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(10): Show |
3 | a0001c0001t0001g0176 a0001c0001t0001g0272 a0001c0001t0001g0281 |
3 | HG00438.hp1 NA18612.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.185+933_185+934ins others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(12): Show |
1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.185+933_185+934ins others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | GAAAAAAA others(14): Show |
1 | a0001c0001t0005g0339 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.185+933_185+934ins others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | ||||||
| chr9:125300023 | G | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+917G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300023 | |||||||
| chr9:125300028 | A | T | 1 | a0001c0003t0004g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+922A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300028 | |||||||
| chr9:125300036 | AAAATATA others(23): Show |
A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+932_185+961del others(30): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300036 | ||||||
| chr9:125300037 | AAATATAT others(4): Show |
A | 4 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0137 others(1): Show |
4 | HG01167.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+933_185+943del others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300037 | ||||||
| chr9:125300037 | AAATATAT others(6): Show |
A | 1 | a0001c0003t0006g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.185+933_185+945del others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300037 | ||||||
| chr9:125300038 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0241 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.185+933_185+934ins others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0242 a0001c0001t0010g0263 |
2 | HG01515.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.185+933_185+934ins others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATAT | A | 8 | a0001c0001t0001g0237 a0001c0001t0001g0268 a0001c0001t0001g0297 others(5): Show |
8 | HG00423.hp2 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+983_185+988del others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(1): Show |
A | 13 | a0001c0001t0001g0247 a0001c0001t0001g0250 a0001c0001t0001g0305 others(10): Show |
13 | HG00735.hp1 HG01346.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+981_185+988del others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(3): Show |
A | 7 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0319 others(4): Show |
7 | HG02451.hp1 HG02559.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+979_185+988del others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(5): Show |
A | 10 | a0001c0001t0001g0324 a0001c0001t0002g0036 a0001c0001t0002g0040 others(7): Show |
10 | HG00558.hp2 HG01192.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+977_185+988del others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(7): Show |
A | 16 | a0001c0001t0001g0323 a0001c0001t0002g0106 a0001c0001t0002g0308 others(13): Show |
16 | HG00738.hp1 HG01993.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+975_185+988del others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(9): Show |
A | 25 | a0001c0001t0001g0018 a0001c0001t0002g0024 a0001c0001t0002g0062 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.185+973_185+988del others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(11): Show |
A | 4 | a0001c0001t0002g0094 a0001c0001t0002g0114 a0001c0001t0002g0116 others(1): Show |
4 | HG02165.hp2 HG04228.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+971_185+988del others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+967_185+988del others(22): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300038 | AATATATA others(31): Show |
A | 1 | a0001c0003t0006g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+951_185+988del others(38): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | ||||||
| chr9:125300039 | ATAT | A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0234 a0001c0001t0002g0122 |
3 | HG03491.hp1 NA18967.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.185+934_185+936del others(3): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATAT | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0206 a0001c0001t0001g0219 |
3 | HG02083.hp2 HG02683.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.185+934_185+938del others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT | A | 8 | a0001c0001t0001g0248 a0001c0001t0001g0309 a0001c0001t0001g0320 others(5): Show |
8 | HG01517.hp2 HG02056.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+934_185+940del others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(2): Show |
A | 13 | a0001c0001t0001g0317 a0001c0001t0002g0025 a0001c0001t0002g0027 others(10): Show |
13 | HG00423.hp1 HG00673.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+934_185+942del others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(4): Show |
A | 27 | a0001c0001t0001g0325 a0001c0001t0002g0017 a0001c0001t0002g0029 others(24): Show |
27 | HG00140.hp1 HG00621.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+934_185+944del others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(6): Show |
A | 6 | a0001c0001t0002g0030 a0001c0001t0002g0055 a0001c0001t0002g0083 others(3): Show |
6 | HG00280.hp2 HG02055.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+934_185+946del others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(8): Show |
A | 22 | a0001c0001t0001g0052 a0001c0001t0001g0200 a0001c0001t0001g0261 others(19): Show |
22 | HG00544.hp2 HG01123.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+934_185+948del others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(10): Show |
A | 22 | a0001c0001t0002g0016 a0001c0001t0002g0051 a0001c0001t0002g0069 others(19): Show |
22 | HG00099.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+934_185+950del others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(12): Show |
A | 4 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0059 others(1): Show |
4 | HG01069.hp2 HG02165.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+934_185+952del others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.185+934_185+954del others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(16): Show |
A | 5 | a0001c0001t0005g0328 a0001c0001t0005g0332 a0001c0001t0005g0335 others(2): Show |
5 | HG00741.hp2 NA18961.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+934_185+956del others(23): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0009g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185+934_185+960del others(27): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300039 | ATATATAT others(22): Show |
A | 2 | a0001c0001t0009g0003 a0001c0001t0009g0004 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.185+934_185+962del others(29): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | |||||||
| chr9:125300040 | T | A | 111 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(108): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.185+934T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300040 | |||||||
| chr9:125300042 | T | A | 105 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(102): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.185+936T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300042 | |||||||
| chr9:125300044 | T | A | 103 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.185+938T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300044 | |||||||
| chr9:125300046 | T | A | 101 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.185+940T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300046 | |||||||
| chr9:125300048 | T | A | 97 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(94): Show |
97 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.185+942T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300048 | |||||||
| chr9:125300050 | T | A | 92 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0192 others(89): Show |
92 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.185+944T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300050 | |||||||
| chr9:125300051 | AT | A | 3 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0137 |
3 | HG01167.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.185+946delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300051 | |||||||
| chr9:125300052 | T | A | 117 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0206 others(114): Show |
117 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.185+946T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300052 | |||||||
| chr9:125300054 | T | A | 123 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0206 others(120): Show |
123 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.185+948T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300054 | |||||||
| chr9:125300056 | T | A | 159 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0192 others(156): Show |
159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.185+950T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300056 | |||||||
| chr9:125300058 | T | A | 171 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0192 others(168): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.185+952T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300058 | |||||||
| chr9:125300060 | T | A | 149 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0192 others(146): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.185+954T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300060 | |||||||
| chr9:125300062 | T | A | 137 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0192 others(134): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.185+956T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300062 | |||||||
| chr9:125300064 | T | A | 111 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0192 others(108): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.185+958T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300064 | |||||||
| chr9:125300066 | T | A | 96 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0200 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.185+960T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300066 | |||||||
| chr9:125300068 | T | A | 59 | a0001c0001t0001g0018 a0001c0001t0001g0200 a0001c0001t0001g0203 others(56): Show |
59 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.185+962T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300068 | |||||||
| chr9:125300070 | T | A | 30 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0001g0227 others(27): Show |
30 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.185+964T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300070 | |||||||
| chr9:125300072 | T | A | 9 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0001t0002g0070 others(6): Show |
9 | HG00741.hp2 HG02074.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+966T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300072 | |||||||
| chr9:125300074 | T | A | 7 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0001t0005g0328 others(4): Show |
7 | HG00741.hp2 HG02602.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+968T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300074 | |||||||
| chr9:125300076 | T | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0001t0005g0328 others(3): Show |
6 | HG00741.hp2 HG02602.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+970T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300076 | |||||||
| chr9:125300078 | T | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0001t0014g0260 others(1): Show |
4 | HG00741.hp2 HG02572.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+972T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300078 | |||||||
| chr9:125300080 | T | A | 1 | a0001c0001t0014g0260 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.185+974T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300080 | |||||||
| chr9:125300095 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+989G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300095 | |||||||
| chr9:125300156 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.185+1050C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300156 | |||||||
| chr9:125300189 | T | A | 239 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(236): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.185+1083T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300189 | |||||||
| chr9:125300203 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.185+1097T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300203 | |||||||
| chr9:125300212 | C | T | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.185+1106C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300212 | |||||||
| chr9:125300583 | A | G | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.186-1400A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300583 | |||||||
| chr9:125300933 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.186-1050T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300933 | |||||||
| chr9:125300946 | G | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186-1037G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300946 | |||||||
| chr9:125301074 | A | AT | 34 | a0001c0001t0002g0114 a0001c0001t0028g0113 a0001c0002t0003g0005 others(31): Show |
34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.186-896dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125301074 | ||||||
| chr9:125301206 | C | T | 2 | a0001c0001t0001g0318 a0001c0001t0001g0320 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.186-777C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301206 | |||||||
| chr9:125301623 | A | G | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.186-360A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301623 | |||||||
| chr9:125301715 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.186-268G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301715 | |||||||
| chr9:125301739 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0252 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.186-244C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301739 | |||||||
| chr9:125301860 | T | C | 1 | a0001c0005t0001g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.186-123T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301860 | |||||||
| chr9:125301963 | C | CTT | 30 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(27): Show |
30 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
splice_acceptor_variant&intron_variant | HIGH | c.186-4_186-3dupTT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125301963 | ||||||
| chr9:125301963 | CT | C | 19 | a0001c0001t0001g0232 a0001c0001t0002g0064 a0001c0001t0002g0308 others(16): Show |
19 | HG01069.hp2 HG01167.hp1 HG01257.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.186-3delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125301963 | ||||||
| chr9:125303005 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1029+179A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303005 | |||||||
| chr9:125303009 | C | A | 9 | a0001c0001t0001g0272 a0001c0001t0001g0279 a0001c0001t0001g0281 others(6): Show |
9 | HG00438.hp1 HG00621.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029+183C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303009 | |||||||
| chr9:125303129 | A | G | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0274 others(1): Show |
4 | HG01255.hp1 NA18952.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1029+303A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303129 | |||||||
| chr9:125303478 | TA | T | 6 | a0001c0001t0001g0261 a0001c0001t0002g0015 a0001c0001t0002g0016 others(3): Show |
6 | HG01167.hp2 NA18939.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029+666delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr9 | 125303478 | ||||||
| chr9:125303552 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1029+726G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303552 | |||||||
| chr9:125303656 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1029+830A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303656 | |||||||
| chr9:125303776 | C | CA | 215 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(212): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1029+966dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr9 | 125303776 | ||||||
| chr9:125303776 | C | CAA | 10 | a0001c0001t0001g0254 a0001c0001t0004g0172 a0001c0001t0004g0173 others(7): Show |
10 | HG01099.hp1 HG01167.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1029+965_1029+966d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr9 | 125303776 | ||||||
| chr9:125303885 | T | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0292 |
2 | NA18974.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1029+1059T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303885 | |||||||
| chr9:125303892 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1029+1066T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303892 | |||||||
| chr9:125303996 | A | G | 1 | a0001c0003t0006g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1030-1067A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303996 | |||||||
| chr9:125303999 | T | G | 1 | a0001c0001t0002g0043 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1030-1064T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303999 | |||||||
| chr9:125304122 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1030-941A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304122 | |||||||
| chr9:125304334 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1030-729C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304334 | |||||||
| chr9:125304671 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1030-392C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304671 | |||||||
| chr9:125304857 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1030-206T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304857 | |||||||
| chr9:125304942 | G | A | 8 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0146 others(5): Show |
8 | NA18939.hp1 NA18968.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-121G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304942 | |||||||
| chr9:125305002 | A | G | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1030-61A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125305002 | |||||||
| chr9:125305017 | T | C | 7 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1030-46T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125305017 | |||||||
| chr9:125305223 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1116+74C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305223 | |||||||
| chr9:125305329 | T | C | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+180T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305329 | |||||||
| chr9:125305371 | G | GT | 11 | a0001c0001t0002g0025 a0001c0001t0002g0071 a0001c0001t0002g0074 others(8): Show |
11 | HG00621.hp1 NA18949.hp1 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.1116+242dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125305371 | ||||||
| chr9:125305371 | GT | G | 169 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(166): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1116+242delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125305371 | ||||||
| chr9:125305371 | GTT | G | 15 | a0001c0001t0001g0311 a0001c0001t0009g0002 a0001c0001t0009g0003 others(12): Show |
15 | HG01109.hp1 HG01167.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1116+241_1116+242d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125305371 | ||||||
| chr9:125305402 | C | T | 1 | a0001c0003t0006g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1116+253C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305402 | |||||||
| chr9:125305620 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0234 |
2 | NA18967.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1116+471C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305620 | |||||||
| chr9:125305667 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1116+518C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305667 | |||||||
| chr9:125305798 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1116+649G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305798 | |||||||
| chr9:125306035 | C | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116+886C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306035 | |||||||
| chr9:125306109 | G | A | 103 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(100): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.1116+960G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306109 | |||||||
| chr9:125306268 | A | G | 2 | a0001c0001t0025g0205 a0001c0001t0034g0214 |
2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1116+1119A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306268 | |||||||
| chr9:125306388 | G | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1117-1025G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306388 | |||||||
| chr9:125306458 | T | C | 1 | a0001c0001t0002g0027 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1117-955T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306458 | |||||||
| chr9:125306715 | A | G | 1 | a0001c0003t0004g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1117-698A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306715 | |||||||
| chr9:125306720 | C | T | 2 | a0001c0001t0001g0318 a0001c0001t0001g0320 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1117-693C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306720 | |||||||
| chr9:125306758 | G | T | 1 | a0003c0007t0001g0307 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1117-655G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306758 | |||||||
| chr9:125306834 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA18963.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1117-579T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306834 | |||||||
| chr9:125306881 | G | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1117-532G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306881 | |||||||
| chr9:125306945 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1117-468C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306945 | |||||||
| chr9:125307084 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1117-329G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307084 | |||||||
| chr9:125307133 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1117-280G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307133 | |||||||
| chr9:125307157 | C | T | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1117-256C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307157 | |||||||
| chr9:125307201 | A | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1117-212A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307201 | |||||||
| chr9:125307229 | A | G | 2 | a0001c0001t0030g0141 a0001c0016t0037g0171 |
2 | HG02135.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1117-184A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307229 | |||||||
| chr9:125307268 | C | CA | 19 | a0001c0001t0001g0178 a0001c0001t0001g0208 a0001c0001t0001g0212 others(16): Show |
19 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1117-128dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125307268 | ||||||
| chr9:125307361 | G | A | 1 | a0001c0001t0025g0205 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1117-52G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307361 | |||||||
| chr9:125307598 | G | A | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1251+51G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 7/27 | chr9 | 125307598 | |||||||
| chr9:125307676 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1252-15C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 7/27 | chr9 | 125307676 | |||||||
| chr9:125307948 | G | C | 198 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(195): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1441+68G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125307948 | |||||||
| chr9:125308217 | G | A | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441+337G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308217 | |||||||
| chr9:125308231 | T | A | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1441+351T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308231 | |||||||
| chr9:125308326 | ACC | A | 335 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(332): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1441+448_1441+449d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125308326 | ||||||
| chr9:125308330 | T | A | 335 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(332): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1441+450T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308330 | |||||||
| chr9:125308347 | C | CA | 17 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(14): Show |
17 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1441+481dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125308347 | ||||||
| chr9:125308347 | CA | C | 35 | a0001c0001t0002g0097 a0001c0001t0017g0014 a0001c0002t0003g0005 others(32): Show |
35 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1441+481delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125308347 | ||||||
| chr9:125308461 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1441+581A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308461 | |||||||
| chr9:125308475 | C | T | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1441+595C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308475 | |||||||
| chr9:125308513 | A | G | 335 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(332): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1441+633A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308513 | |||||||
| chr9:125308650 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1441+770G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308650 | |||||||
| chr9:125308738 | G | A | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1441+858G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308738 | |||||||
| chr9:125308768 | C | G | 1 | a0001c0002t0003g0170 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1441+888C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308768 | |||||||
| chr9:125308830 | A | G | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(2): Show |
5 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441+950A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308830 | |||||||
| chr9:125308898 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1441+1018T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308898 | |||||||
| chr9:125308912 | A | G | 34 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(31): Show |
34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1441+1032A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308912 | |||||||
| chr9:125308960 | T | C | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1441+1080T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308960 | |||||||
| chr9:125309192 | C | T | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441+1312C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309192 | |||||||
| chr9:125309240 | T | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1441+1360T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309240 | |||||||
| chr9:125309323 | T | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1441+1443T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309323 | |||||||
| chr9:125309335 | G | A | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441+1455G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309335 | |||||||
| chr9:125309375 | C | G | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1441+1495C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309375 | |||||||
| chr9:125309499 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0252 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1441+1619T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309499 | |||||||
| chr9:125309587 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1441+1707G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309587 | |||||||
| chr9:125309605 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1441+1725G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309605 | |||||||
| chr9:125309754 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1441+1874G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309754 | |||||||
| chr9:125309994 | G | C | 201 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(198): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1441+2114G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309994 | |||||||
| chr9:125310427 | T | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1442-2025T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310427 | |||||||
| chr9:125310537 | A | AT | 6 | a0001c0001t0002g0017 a0001c0001t0002g0033 a0001c0001t0002g0080 others(3): Show |
6 | HG00544.hp1 HG01175.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1442-1896dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310537 | ||||||
| chr9:125310537 | AT | A | 45 | a0001c0001t0001g0178 a0001c0001t0002g0035 a0001c0001t0002g0119 others(42): Show |
45 | HG00140.hp1 HG00544.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1442-1896delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310537 | ||||||
| chr9:125310537 | ATT | A | 185 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(182): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1442-1897_1442-189 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310537 | ||||||
| chr9:125310644 | A | G | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-1808A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310644 | |||||||
| chr9:125310705 | ATTTTGTA others(296): Show |
A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1442-1726_1442-142 others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310705 | ||||||
| chr9:125310801 | G | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1442-1651G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310801 | |||||||
| chr9:125310818 | G | A | 228 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(225): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1442-1634G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310818 | |||||||
| chr9:125310843 | CT | C | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-1595delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310843 | ||||||
| chr9:125310903 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1442-1549G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310903 | |||||||
| chr9:125311029 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-1423C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311029 | |||||||
| chr9:125311061 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1442-1391A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311061 | |||||||
| chr9:125311207 | C | A | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-1245C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311207 | |||||||
| chr9:125311207 | C | G | 1 | a0001c0001t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1442-1245C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311207 | |||||||
| chr9:125311221 | T | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1442-1231T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311221 | |||||||
| chr9:125311265 | A | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-1187A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311265 | |||||||
| chr9:125311451 | G | C | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-1001G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311451 | |||||||
| chr9:125311538 | T | G | 1 | a0001c0013t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1442-914T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311538 | |||||||
| chr9:125311559 | C | T | 7 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0305 others(4): Show |
7 | HG02056.hp1 NA18942.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1442-893C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311559 | |||||||
| chr9:125311580 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1442-872C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311580 | |||||||
| chr9:125311724 | CT | C | 162 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(159): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1442-715delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125311724 | ||||||
| chr9:125311988 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1442-464A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311988 | |||||||
| chr9:125312082 | G | A | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-370G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125312082 | |||||||
| chr9:125312319 | C | G | 1 | a0001c0001t0004g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442-133C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125312319 | |||||||
| chr9:125313111 | C | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1602+499C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313111 | |||||||
| chr9:125313112 | G | A | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1602+500G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313112 | |||||||
| chr9:125313264 | A | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1602+652A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313264 | |||||||
| chr9:125313439 | G | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0069 |
2 | HG00099.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1602+827G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313439 | |||||||
| chr9:125313592 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+980C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313592 | |||||||
| chr9:125313790 | G | A | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1602+1178G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313790 | |||||||
| chr9:125313827 | C | T | 1 | a0001c0001t0036g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1602+1215C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313827 | |||||||
| chr9:125313890 | T | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+1278T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313890 | |||||||
| chr9:125313943 | A | G | 3 | a0001c0001t0010g0213 a0001c0001t0010g0253 a0001c0001t0010g0263 |
3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1602+1331A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313943 | |||||||
| chr9:125314011 | G | C | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+1399G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314011 | |||||||
| chr9:125314054 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0240 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+1442C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314054 | |||||||
| chr9:125314176 | T | G | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+1564T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314176 | |||||||
| chr9:125314239 | G | A | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+1627G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314239 | |||||||
| chr9:125314262 | A | G | 198 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(195): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1602+1650A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314262 | |||||||
| chr9:125314340 | A | G | 1 | a0001c0003t0026g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1602+1728A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314340 | |||||||
| chr9:125314480 | A | C | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+1868A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314480 | |||||||
| chr9:125314520 | G | A | 1 | a0001c0001t0004g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1602+1908G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314520 | |||||||
| chr9:125314624 | A | G | 200 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(197): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1602+2012A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314624 | |||||||
| chr9:125314653 | TCAAAACA others(3): Show |
T | 2 | a0003c0007t0001g0300 a0003c0007t0001g0307 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1602+2057_1602+206 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125314653 | ||||||
| chr9:125314681 | CAG | C | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602+2071_1602+207 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125314681 | ||||||
| chr9:125314702 | C | G | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1602+2090C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314702 | |||||||
| chr9:125314789 | C | CT | 7 | a0001c0001t0001g0297 a0001c0001t0002g0079 a0001c0001t0004g0172 others(4): Show |
7 | HG01099.hp1 HG01109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602+2193dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125314789 | ||||||
| chr9:125314826 | C | T | 1 | a0001c0001t0015g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1602+2214C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314826 | |||||||
| chr9:125314839 | G | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+2227G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314839 | |||||||
| chr9:125314856 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1602+2244C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314856 | |||||||
| chr9:125314949 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1602+2337G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314949 | |||||||
| chr9:125314996 | C | T | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1602+2384C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314996 | |||||||
| chr9:125315019 | C | G | 3 | a0001c0001t0002g0107 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | HG00408.hp2 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1602+2407C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315019 | |||||||
| chr9:125315022 | C | T | 10 | a0001c0001t0001g0191 a0001c0001t0001g0268 a0001c0001t0001g0297 others(7): Show |
10 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1602+2410C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315022 | |||||||
| chr9:125315031 | C | T | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+2419C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315031 | |||||||
| chr9:125315053 | C | G | 1 | a0001c0001t0002g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1602+2441C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315053 | |||||||
| chr9:125315060 | T | C | 1 | a0001c0010t0006g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1602+2448T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315060 | |||||||
| chr9:125315255 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1602+2643A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315255 | |||||||
| chr9:125315345 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+2733C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315345 | |||||||
| chr9:125315519 | A | C | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1602+2907A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315519 | |||||||
| chr9:125315561 | G | A | 9 | a0001c0002t0003g0149 a0001c0002t0003g0152 a0001c0002t0003g0155 others(6): Show |
9 | HG01081.hp2 HG02129.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1602+2949G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315561 | |||||||
| chr9:125315824 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1602+3212G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315824 | |||||||
| chr9:125315892 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1602+3280G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315892 | |||||||
| chr9:125315957 | C | T | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+3345C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315957 | |||||||
| chr9:125316062 | C | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+3450C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316062 | |||||||
| chr9:125316308 | C | G | 9 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0068 others(6): Show |
9 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1602+3696C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316308 | |||||||
| chr9:125316308 | C | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+3696C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316308 | |||||||
| chr9:125316327 | T | C | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+3715T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316327 | |||||||
| chr9:125316328 | A | T | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+3716A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316328 | |||||||
| chr9:125316330 | C | A | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+3718C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316330 | |||||||
| chr9:125316580 | T | C | 1 | a0001c0003t0006g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1602+3968T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316580 | |||||||
| chr9:125316617 | G | A | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1602+4005G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316617 | |||||||
| chr9:125316637 | T | C | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1602+4025T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316637 | |||||||
| chr9:125316697 | C | T | 3 | a0001c0002t0003g0166 a0002c0006t0011g0142 a0002c0006t0011g0143 |
3 | HG01109.hp2 HG03098.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1602+4085C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316697 | |||||||
| chr9:125316969 | T | C | 2 | a0001c0001t0001g0259 a0005c0017t0001g0249 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1602+4357T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316969 | |||||||
| chr9:125317156 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1603-4277A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317156 | |||||||
| chr9:125317179 | G | A | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603-4254G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317179 | |||||||
| chr9:125317304 | C | T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1603-4129C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317304 | |||||||
| chr9:125317317 | C | CA | 7 | a0001c0001t0002g0074 a0001c0001t0002g0139 a0001c0001t0013g0190 others(4): Show |
7 | HG01109.hp2 HG01175.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-4103dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125317317 | ||||||
| chr9:125317360 | T | C | 1 | a0001c0001t0022g0280 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1603-4073T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317360 | |||||||
| chr9:125317372 | T | C | 2 | a0001c0002t0003g0152 a0001c0002t0007g0148 |
2 | HG01081.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1603-4061T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317372 | |||||||
| chr9:125317410 | G | C | 1 | a0001c0003t0006g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1603-4023G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317410 | |||||||
| chr9:125317612 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-3821C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317612 | |||||||
| chr9:125317623 | CT | C | 30 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(27): Show |
30 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1603-3809delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317623 | |||||||
| chr9:125317624 | T | A | 1 | a0001c0002t0003g0146 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1603-3809T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317624 | |||||||
| chr9:125317625 | C | A | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-3808C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317625 | |||||||
| chr9:125317625 | C | CA | 10 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0179 others(7): Show |
10 | HG02027.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-3791dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125317625 | ||||||
| chr9:125317625 | C | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1603-3808C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317625 | |||||||
| chr9:125317742 | A | G | 14 | a0001c0001t0001g0299 a0001c0001t0001g0302 a0001c0001t0001g0303 others(11): Show |
14 | HG02004.hp1 HG02056.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1603-3691A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317742 | |||||||
| chr9:125317816 | G | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-3617G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317816 | |||||||
| chr9:125317973 | G | A | 1 | a0002c0006t0011g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1603-3460G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317973 | |||||||
| chr9:125317977 | A | C | 1 | a0001c0003t0006g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1603-3456A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317977 | |||||||
| chr9:125318095 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1603-3338C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318095 | |||||||
| chr9:125318109 | C | G | 2 | a0001c0003t0006g0135 a0001c0003t0006g0138 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-3324C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318109 | |||||||
| chr9:125318359 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1603-3074A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318359 | |||||||
| chr9:125318509 | A | G | 7 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-2924A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318509 | |||||||
| chr9:125318667 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0186 |
2 | HG00558.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1603-2766A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318667 | |||||||
| chr9:125318736 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1603-2697G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318736 | |||||||
| chr9:125318907 | G | T | 56 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(53): Show |
56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1603-2526G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318907 | |||||||
| chr9:125318908 | G | T | 56 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(53): Show |
56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1603-2525G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318908 | |||||||
| chr9:125318990 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0252 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1603-2443A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318990 | |||||||
| chr9:125319157 | A | C | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1603-2276A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319157 | |||||||
| chr9:125319211 | T | TA | 336 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1603-2218dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125319211 | ||||||
| chr9:125319380 | T | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1603-2053T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319380 | |||||||
| chr9:125319390 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1603-2043T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319390 | |||||||
| chr9:125319430 | A | C | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-2003A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319430 | |||||||
| chr9:125319563 | C | G | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1603-1870C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319563 | |||||||
| chr9:125319601 | C | CT | 14 | a0001c0001t0001g0271 a0001c0001t0001g0284 a0001c0001t0001g0291 others(11): Show |
14 | HG01175.hp1 HG02004.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1603-1814dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125319601 | ||||||
| chr9:125319627 | A | G | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603-1806A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319627 | |||||||
| chr9:125319704 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1603-1729C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319704 | |||||||
| chr9:125319903 | A | C | 2 | a0001c0005t0001g0216 a0001c0005t0001g0224 |
2 | HG00280.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1603-1530A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319903 | |||||||
| chr9:125319950 | A | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1603-1483A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319950 | |||||||
| chr9:125320054 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1603-1379A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320054 | |||||||
| chr9:125320061 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0184 |
2 | NA18952.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1603-1372T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320061 | |||||||
| chr9:125320109 | C | T | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1603-1324C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320109 | |||||||
| chr9:125320289 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1603-1144A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320289 | |||||||
| chr9:125320294 | C | A | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-1139C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320294 | |||||||
| chr9:125320376 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0002g0256 |
2 | HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1603-1057A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320376 | |||||||
| chr9:125320480 | G | A | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-953G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320480 | |||||||
| chr9:125320531 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1603-902C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320531 | |||||||
| chr9:125320726 | C | T | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1603-707C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320726 | |||||||
| chr9:125320767 | A | G | 1 | a0001c0001t0002g0033 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1603-666A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320767 | |||||||
| chr9:125320820 | G | T | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-613G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320820 | |||||||
| chr9:125320823 | T | A | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-610T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320823 | |||||||
| chr9:125320861 | C | T | 3 | a0001c0001t0001g0180 a0002c0006t0011g0142 a0002c0006t0011g0143 |
3 | HG01109.hp2 HG03098.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1603-572C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320861 | |||||||
| chr9:125320884 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1603-549C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320884 | |||||||
| chr9:125320906 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1603-527G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320906 | |||||||
| chr9:125320913 | T | A | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-520T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320913 | |||||||
| chr9:125320917 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1603-516C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320917 | |||||||
| chr9:125321288 | T | A | 1 | a0006c0011t0005g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-145T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321288 | |||||||
| chr9:125321306 | T | C | 2 | a0001c0001t0001g0288 a0001c0001t0001g0312 |
2 | NA18959.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1603-127T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321306 | |||||||
| chr9:125321310 | A | C | 2 | a0001c0005t0001g0216 a0001c0005t0001g0224 |
2 | HG00280.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1603-123A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321310 | |||||||
| chr9:125321356 | A | G | 1 | a0001c0002t0003g0144 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1603-77A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321356 | |||||||
| chr9:125321886 | G | T | 199 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1732+324G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321886 | |||||||
| chr9:125321890 | C | T | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1732+328C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321890 | |||||||
| chr9:125321904 | C | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1732+342C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321904 | |||||||
| chr9:125321981 | G | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1732+419G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321981 | |||||||
| chr9:125322113 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1732+551G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322113 | |||||||
| chr9:125322125 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1732+563C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322125 | |||||||
| chr9:125322126 | G | C | 1 | a0001c0001t0002g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1732+564G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322126 | |||||||
| chr9:125322157 | C | T | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1732+595C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322157 | |||||||
| chr9:125322254 | C | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0183 others(3): Show |
6 | HG00558.hp1 NA18973.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1732+692C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322254 | |||||||
| chr9:125322265 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1732+703C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322265 | |||||||
| chr9:125322285 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1732+723C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322285 | |||||||
| chr9:125322353 | C | T | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1732+791C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322353 | |||||||
| chr9:125322359 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1732+797T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322359 | |||||||
| chr9:125322363 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1732+801C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322363 | |||||||
| chr9:125322478 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1732+916T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322478 | |||||||
| chr9:125322517 | A | G | 6 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1732+955A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322517 | |||||||
| chr9:125322690 | T | TG | 231 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(228): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1733-1106dupG | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr9 | 125322690 | ||||||
| chr9:125322977 | A | G | 200 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(197): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1733-821A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322977 | |||||||
| chr9:125323051 | T | TA | 13 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0269 others(10): Show |
13 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1733-729dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr9 | 125323051 | ||||||
| chr9:125323051 | TA | T | 7 | a0001c0001t0001g0202 a0001c0001t0001g0234 a0001c0001t0002g0031 others(4): Show |
7 | HG02922.hp1 HG03491.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1733-729delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr9 | 125323051 | ||||||
| chr9:125323064 | A | G | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733-734A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323064 | |||||||
| chr9:125323067 | A | G | 12 | a0001c0001t0002g0073 a0001c0003t0004g0020 a0001c0003t0004g0021 others(9): Show |
12 | HG01167.hp1 HG02071.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1733-731A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323067 | |||||||
| chr9:125323148 | C | T | 34 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(31): Show |
34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1733-650C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323148 | |||||||
| chr9:125323166 | A | G | 231 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(228): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1733-632A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323166 | |||||||
| chr9:125323169 | C | T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1733-629C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323169 | |||||||
| chr9:125323198 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1733-600C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323198 | |||||||
| chr9:125323200 | G | A | 157 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(154): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1733-598G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323200 | |||||||
| chr9:125323242 | G | C | 1 | a0001c0001t0002g0106 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1733-556G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323242 | |||||||
| chr9:125323252 | A | G | 1 | a0001c0001t0002g0016 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1733-546A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323252 | |||||||
| chr9:125323754 | T | C | 31 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1733-44T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323754 | |||||||
| chr9:125323997 | A | G | 1 | a0001c0001t0002g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1858+74A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125323997 | |||||||
| chr9:125324397 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1858+474C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324397 | |||||||
| chr9:125324405 | A | G | 1 | a0001c0001t0025g0205 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1858+482A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324405 | |||||||
| chr9:125324453 | G | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1858+530G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324453 | |||||||
| chr9:125324478 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1858+555A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324478 | |||||||
| chr9:125324543 | C | T | 1 | a0001c0001t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1858+620C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324543 | |||||||
| chr9:125324689 | G | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1858+766G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324689 | |||||||
| chr9:125324732 | G | C | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1858+809G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324732 | |||||||
| chr9:125324838 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1858+915A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324838 | |||||||
| chr9:125324850 | G | C | 2 | a0001c0002t0003g0146 a0001c0002t0003g0165 |
2 | NA18988.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1858+927G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324850 | |||||||
| chr9:125324916 | G | A | 1 | a0001c0003t0004g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1858+993G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324916 | |||||||
| chr9:125324921 | G | C | 92 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0195 others(89): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1858+998G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324921 | |||||||
| chr9:125324960 | C | T | 1 | a0001c0001t0004g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1858+1037C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324960 | |||||||
| chr9:125325260 | A | G | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1859-1156A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325260 | |||||||
| chr9:125325294 | A | G | 231 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(228): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1859-1122A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325294 | |||||||
| chr9:125325393 | G | T | 33 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(30): Show |
33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1859-1023G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325393 | |||||||
| chr9:125325509 | G | A | 1 | a0001c0001t0024g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1859-907G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325509 | |||||||
| chr9:125325519 | C | CA | 161 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(158): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1859-877dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr9 | 125325519 | ||||||
| chr9:125325519 | CA | C | 70 | a0001c0001t0002g0019 a0001c0001t0002g0029 a0001c0001t0002g0041 others(67): Show |
70 | HG00544.hp2 HG00621.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.1859-877delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr9 | 125325519 | ||||||
| chr9:125325616 | C | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1859-800C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325616 | |||||||
| chr9:125325632 | C | A | 1 | a0001c0003t0004g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1859-784C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325632 | |||||||
| chr9:125325671 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1859-745A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325671 | |||||||
| chr9:125325712 | T | C | 3 | a0001c0001t0001g0317 a0001c0001t0001g0319 a0001c0001t0001g0321 |
3 | HG02451.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1859-704T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325712 | |||||||
| chr9:125325954 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1859-462A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325954 | |||||||
| chr9:125326065 | G | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0016 |
2 | NA18977.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1859-351G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326065 | |||||||
| chr9:125326069 | C | T | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1859-347C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326069 | |||||||
| chr9:125326207 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1859-209A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326207 | |||||||
| chr9:125326236 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1859-180G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326236 | |||||||
| chr9:125326240 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1859-176A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326240 | |||||||
| chr9:125326316 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1859-100G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326316 | |||||||
| chr9:125326716 | T | C | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2032+127T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125326716 | |||||||
| chr9:125326826 | C | CA | 9 | a0001c0001t0002g0027 a0001c0001t0004g0007 a0001c0001t0004g0008 others(6): Show |
9 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2032+249dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125326826 | ||||||
| chr9:125327139 | G | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2032+550G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327139 | |||||||
| chr9:125327397 | T | A | 1 | a0001c0001t0001g0325 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2032+808T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327397 | |||||||
| chr9:125327439 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2032+850G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327439 | |||||||
| chr9:125327479 | T | C | 165 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(162): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2032+890T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327479 | |||||||
| chr9:125327482 | T | C | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2032+893T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327482 | |||||||
| chr9:125327529 | G | A | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2032+940G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327529 | |||||||
| chr9:125327606 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0240 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032+1017T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327606 | |||||||
| chr9:125327663 | C | A | 7 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2032+1074C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327663 | |||||||
| chr9:125327665 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2032+1076A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327665 | |||||||
| chr9:125328134 | T | C | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2032+1545T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328134 | |||||||
| chr9:125328188 | C | CT | 61 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(58): Show |
61 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2032+1616dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328188 | ||||||
| chr9:125328188 | CT | C | 38 | a0001c0001t0002g0026 a0001c0001t0002g0075 a0001c0001t0002g0097 others(35): Show |
38 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.2032+1616delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328188 | ||||||
| chr9:125328189 | T | C | 1 | a0001c0001t0008g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2032+1600T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328189 | |||||||
| chr9:125328205 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2032+1616T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328205 | |||||||
| chr9:125328205 | TA | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0232 a0001c0001t0001g0236 others(2): Show |
5 | HG01074.hp1 HG01167.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2032+1619delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328205 | ||||||
| chr9:125328206 | A | T | 114 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(111): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2032+1617A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328206 | |||||||
| chr9:125328333 | C | T | 1 | a0001c0002t0003g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2032+1744C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328333 | |||||||
| chr9:125328390 | G | T | 229 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2033-1688G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328390 | |||||||
| chr9:125328454 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1624T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328454 | |||||||
| chr9:125328615 | G | C | 1 | a0001c0001t0002g0023 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2033-1463G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328615 | |||||||
| chr9:125328616 | G | A | 1 | a0001c0001t0002g0023 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2033-1462G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328616 | |||||||
| chr9:125328636 | A | G | 2 | a0001c0001t0002g0106 a0001c0001t0031g0105 |
2 | HG02132.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2033-1442A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328636 | |||||||
| chr9:125328671 | A | G | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2033-1407A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328671 | |||||||
| chr9:125328710 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2033-1368G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328710 | |||||||
| chr9:125328824 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1254A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328824 | |||||||
| chr9:125328831 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1247T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328831 | |||||||
| chr9:125328833 | ACC | A | 226 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.2033-1236_2033-123 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328833 | ||||||
| chr9:125328836 | C | A | 4 | a0001c0001t0002g0199 a0001c0001t0002g0218 a0001c0001t0002g0255 others(1): Show |
4 | HG00558.hp2 NA18941.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2033-1242C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328836 | |||||||
| chr9:125328839 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2033-1239C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328839 | |||||||
| chr9:125328899 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2033-1179G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328899 | |||||||
| chr9:125328918 | C | T | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2033-1160C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328918 | |||||||
| chr9:125328952 | T | C | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.2033-1126T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328952 | |||||||
| chr9:125329067 | G | A | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2033-1011G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329067 | |||||||
| chr9:125329070 | G | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1008G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329070 | |||||||
| chr9:125329088 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2033-990G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329088 | |||||||
| chr9:125329094 | G | A | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2033-984G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329094 | |||||||
| chr9:125329112 | GGGGAGA | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2033-945_2033-940d others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329112 | ||||||
| chr9:125329222 | C | T | 1 | a0001c0003t0004g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2033-856C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329222 | |||||||
| chr9:125329387 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2033-691A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329387 | |||||||
| chr9:125329400 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2033-678C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329400 | |||||||
| chr9:125329566 | T | C | 1 | a0001c0001t0002g0099 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2033-512T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329566 | |||||||
| chr9:125329634 | G | GT | 14 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0051 others(11): Show |
14 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2033-428dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329634 | ||||||
| chr9:125329634 | GT | G | 11 | a0001c0001t0001g0182 a0001c0001t0001g0238 a0001c0001t0001g0317 others(8): Show |
11 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2033-428delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329634 | ||||||
| chr9:125329634 | GTT | G | 184 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(181): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.2033-429_2033-428d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329634 | ||||||
| chr9:125329637 | T | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2033-441T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329637 | |||||||
| chr9:125329823 | C | T | 17 | a0001c0001t0002g0059 a0001c0001t0002g0071 a0001c0001t0002g0089 others(14): Show |
17 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.2033-255C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329823 | |||||||
| chr9:125329824 | G | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-254G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329824 | |||||||
| chr9:125330015 | C | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-63C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125330015 | |||||||
| chr9:125330381 | C | T | 1 | a0001c0002t0003g0144 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2173+163C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330381 | |||||||
| chr9:125330702 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2173+484G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330702 | |||||||
| chr9:125330745 | C | A | 1 | a0001c0004t0002g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2173+527C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330745 | |||||||
| chr9:125330812 | T | C | 1 | a0001c0002t0007g0169 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2173+594T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330812 | |||||||
| chr9:125330816 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2173+598A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330816 | |||||||
| chr9:125330851 | A | G | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2173+633A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330851 | |||||||
| chr9:125330986 | A | AT | 170 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(167): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2173+778dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr9 | 125330986 | ||||||
| chr9:125330989 | T | C | 1 | a0001c0002t0007g0150 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2173+771T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330989 | |||||||
| chr9:125331076 | G | T | 1 | a0001c0001t0002g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2174-850G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331076 | |||||||
| chr9:125331204 | AT | A | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.2174-708delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr9 | 125331204 | ||||||
| chr9:125331272 | C | T | 31 | a0001c0002t0003g0005 a0001c0002t0003g0006 a0001c0002t0003g0144 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2174-654C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331272 | |||||||
| chr9:125331387 | G | A | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2174-539G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331387 | |||||||
| chr9:125331447 | G | A | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2174-479G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331447 | |||||||
| chr9:125331829 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2174-97C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331829 | |||||||
| chr9:125331862 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2174-64A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331862 | |||||||
| chr9:125331920 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03491.hp1 | splice_region_variant&intron_variant | LOW | c.2174-6A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331920 | |||||||
| chr9:125332125 | A | T | 1 | a0001c0001t0002g0058 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2308+65A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 14/27 | chr9 | 125332125 | |||||||
| chr9:125332292 | G | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2309-218G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 14/27 | chr9 | 125332292 | |||||||
| chr9:125332412 | A | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2309-98A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 14/27 | chr9 | 125332412 | |||||||
| chr9:125333031 | A | T | 2 | a0001c0003t0006g0132 a0001c0003t0006g0134 |
2 | HG01167.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2428+402A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333031 | |||||||
| chr9:125333080 | G | GT | 6 | a0001c0001t0002g0061 a0001c0003t0004g0020 a0001c0003t0004g0021 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2428+461dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125333080 | ||||||
| chr9:125333095 | C | T | 9 | a0001c0001t0002g0019 a0001c0001t0002g0029 a0001c0001t0002g0050 others(6): Show |
9 | NA18954.hp1 NA18957.hp1 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.2428+466C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333095 | |||||||
| chr9:125333369 | C | T | 13 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(10): Show |
13 | HG00558.hp1 HG02027.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.2428+740C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333369 | |||||||
| chr9:125333442 | G | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2428+813G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333442 | |||||||
| chr9:125333485 | C | CT | 44 | a0001c0001t0001g0211 a0001c0001t0001g0222 a0001c0001t0001g0229 others(41): Show |
44 | HG00544.hp2 HG01081.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.2428+876dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125333485 | ||||||
| chr9:125333485 | CT | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0262 a0001c0001t0001g0274 others(5): Show |
8 | HG01099.hp1 HG01109.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2428+876delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125333485 | ||||||
| chr9:125333550 | G | A | 6 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(3): Show |
6 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2428+921G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333550 | |||||||
| chr9:125333551 | C | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2428+922C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333551 | |||||||
| chr9:125333558 | G | A | 3 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0136 |
3 | HG02451.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2428+929G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333558 | |||||||
| chr9:125333882 | T | C | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2428+1253T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333882 | |||||||
| chr9:125333927 | G | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0311 |
2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2428+1298G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333927 | |||||||
| chr9:125334143 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2428+1514A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334143 | |||||||
| chr9:125334170 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2428+1541G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334170 | |||||||
| chr9:125334232 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2428+1603G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334232 | |||||||
| chr9:125334242 | G | A | 4 | a0001c0001t0008g0034 a0001c0001t0008g0054 a0001c0001t0008g0057 others(1): Show |
4 | HG01123.hp2 HG01346.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2428+1613G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334242 | |||||||
| chr9:125334270 | T | TA | 48 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(45): Show |
48 | HG00544.hp2 HG00621.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.2428+1663dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334270 | ||||||
| chr9:125334270 | TA | T | 16 | a0001c0001t0001g0236 a0001c0001t0001g0319 a0001c0001t0002g0064 others(13): Show |
16 | HG01069.hp1 HG01069.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2428+1663delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334270 | ||||||
| chr9:125334323 | A | G | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2428+1694A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334323 | |||||||
| chr9:125334340 | A | C | 2 | a0001c0002t0003g0156 a0001c0002t0003g0158 |
2 | NA18940.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2428+1711A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334340 | |||||||
| chr9:125334390 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2428+1761A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334390 | |||||||
| chr9:125334511 | G | T | 21 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(18): Show |
21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2428+1882G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334511 | |||||||
| chr9:125334658 | G | C | 4 | a0001c0001t0002g0199 a0001c0001t0002g0218 a0001c0001t0002g0255 others(1): Show |
4 | HG00558.hp2 NA18941.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2428+2029G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334658 | |||||||
| chr9:125334678 | G | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2428+2049G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334678 | |||||||
| chr9:125334749 | A | G | 1 | a0004c0008t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2428+2120A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334749 | |||||||
| chr9:125334787 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0090 |
2 | HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2428+2158G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334787 | |||||||
| chr9:125334797 | T | TA | 162 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(159): Show |
162 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2428+2181dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334797 | ||||||
| chr9:125334805 | A | G | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2428+2176A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334805 | |||||||
| chr9:125334827 | GTTTC | G | 3 | a0001c0001t0002g0107 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | HG00408.hp2 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2429-2188_2429-218 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334827 | ||||||
| chr9:125335388 | A | T | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2429-1630A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335388 | |||||||
| chr9:125335403 | C | T | 3 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0013t0002g0048 |
3 | NA18959.hp2 NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2429-1615C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335403 | |||||||
| chr9:125335484 | T | A | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2429-1534T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335484 | |||||||
| chr9:125335550 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2429-1468G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335550 | |||||||
| chr9:125335551 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2429-1467C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335551 | |||||||
| chr9:125335604 | G | A | 1 | a0001c0002t0007g0150 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2429-1414G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335604 | |||||||
| chr9:125335844 | T | C | 1 | a0001c0001t0002g0106 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2429-1174T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335844 | |||||||
| chr9:125336145 | C | CA | 28 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0219 others(25): Show |
28 | HG01109.hp2 HG01167.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.2429-857dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336145 | ||||||
| chr9:125336145 | C | CAAA | 27 | a0001c0001t0016g0053 a0001c0002t0003g0006 a0001c0002t0003g0144 others(24): Show |
27 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2429-859_2429-857d others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336145 | ||||||
| chr9:125336245 | G | A | 1 | a0001c0001t0035g0304 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2429-773G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336245 | |||||||
| chr9:125336276 | A | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2429-742A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336276 | |||||||
| chr9:125336290 | C | CA | 18 | a0001c0001t0002g0016 a0001c0001t0002g0019 a0001c0001t0002g0029 others(15): Show |
18 | HG01515.hp2 HG03688.hp2 NA18949.hp1 others(15): Show |
intron_variant | MODIFIER | c.2429-713dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336290 | ||||||
| chr9:125336290 | CA | C | 16 | a0001c0001t0001g0217 a0001c0001t0001g0272 a0001c0001t0001g0286 others(13): Show |
16 | HG00438.hp1 HG01167.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2429-713delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336290 | ||||||
| chr9:125336290 | CAA | C | 166 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(163): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2429-714_2429-713d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336290 | ||||||
| chr9:125336299 | A | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2429-719A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336299 | |||||||
| chr9:125336306 | C | A | 1 | a0001c0002t0003g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2429-712C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336306 | |||||||
| chr9:125336306 | C | CA | 31 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(28): Show |
31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2429-706dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336306 | ||||||
| chr9:125336313 | C | A | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2429-705C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336313 | |||||||
| chr9:125336313 | CA | C | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG02027.hp2 NA18943.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2429-699delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336313 | ||||||
| chr9:125336578 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2429-440G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336578 | |||||||
| chr9:125336771 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2429-247A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336771 | |||||||
| chr9:125337856 | T | A | 4 | a0001c0003t0006g0124 a0001c0003t0006g0125 a0001c0003t0006g0126 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2877+265T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125337856 | |||||||
| chr9:125337969 | A | G | 1 | a0001c0005t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2877+378A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125337969 | |||||||
| chr9:125337980 | A | G | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2877+389A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125337980 | |||||||
| chr9:125338164 | C | G | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2877+573C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338164 | |||||||
| chr9:125338555 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2877+964C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338555 | |||||||
| chr9:125338927 | ATTTGTGT others(7): Show |
A | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2877+1338_2877+135 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338927 | ||||||
| chr9:125338929 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0211 |
2 | HG03654.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2877+1338T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338929 | |||||||
| chr9:125338929 | T | TTG | 34 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0181 others(31): Show |
34 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.2877+1366_2877+136 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | ||||||
| chr9:125338929 | T | TTGTG | 86 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(83): Show |
86 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2877+1364_2877+136 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | ||||||
| chr9:125338929 | T | TTGTGTG | 5 | a0001c0002t0007g0001 a0001c0012t0001g0285 a0002c0006t0011g0142 others(2): Show |
5 | HG01109.hp2 HG01255.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877+1362_2877+136 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | ||||||
| chr9:125338929 | T | TTGTGTGT others(1): Show |
5 | a0001c0001t0001g0296 a0001c0001t0001g0298 a0001c0001t0010g0213 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.2877+1360_2877+136 others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | ||||||
| chr9:125338929 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2877+1354_2877+136 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | ||||||
| chr9:125338929 | TTGTG | T | 12 | a0001c0001t0002g0060 a0001c0003t0004g0020 a0001c0003t0004g0021 others(9): Show |
12 | HG01167.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2877+1364_2877+136 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | ||||||
| chr9:125338955 | GTGTATA | G | 3 | a0001c0001t0001g0317 a0001c0001t0001g0319 a0001c0001t0001g0321 |
3 | HG02451.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2877+1366_2877+137 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338955 | ||||||
| chr9:125338959 | A | G | 196 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(193): Show |
196 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.2877+1368A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338959 | |||||||
| chr9:125338961 | A | G | 158 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(155): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2877+1370A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338961 | |||||||
| chr9:125338963 | A | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0262 |
3 | HG02280.hp1 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2877+1372A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338963 | |||||||
| chr9:125338965 | A | T | 41 | a0001c0001t0002g0017 a0001c0001t0002g0024 a0001c0001t0002g0030 others(38): Show |
41 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.2877+1374A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338965 | |||||||
| chr9:125339086 | A | G | 6 | a0001c0001t0001g0203 a0001c0003t0004g0020 a0001c0003t0004g0021 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2877+1495A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339086 | |||||||
| chr9:125339229 | G | A | 1 | a0001c0001t0013g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2877+1638G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339229 | |||||||
| chr9:125339363 | A | G | 231 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(228): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2877+1772A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339363 | |||||||
| chr9:125339567 | G | A | 1 | a0001c0001t0008g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2878-1610G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339567 | |||||||
| chr9:125339598 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2878-1579A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339598 | |||||||
| chr9:125339712 | A | G | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2878-1465A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339712 | |||||||
| chr9:125339776 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2878-1401A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339776 | |||||||
| chr9:125339971 | A | G | 2 | a0001c0001t0004g0172 a0001c0001t0004g0173 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2878-1206A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339971 | |||||||
| chr9:125340089 | C | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2878-1088C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340089 | |||||||
| chr9:125340221 | T | A | 335 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(332): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.2878-956T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340221 | |||||||
| chr9:125340269 | C | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2878-908C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340269 | |||||||
| chr9:125340327 | T | G | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.2878-850T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340327 | |||||||
| chr9:125340586 | T | C | 200 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(197): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2878-591T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340586 | |||||||
| chr9:125340787 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2878-390C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340787 | |||||||
| chr9:125340911 | C | T | 231 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(228): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2878-266C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340911 | |||||||
| chr9:125341010 | G | C | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2878-167G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125341010 | |||||||
| chr9:125341517 | A | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2965+253A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341517 | |||||||
| chr9:125341765 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2966-454G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341765 | |||||||
| chr9:125341781 | C | T | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2966-438C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341781 | |||||||
| chr9:125341826 | A | C | 230 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(227): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.2966-393A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341826 | |||||||
| chr9:125341988 | A | G | 1 | a0001c0001t0004g0012 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2966-231A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341988 | |||||||
| chr9:125342594 | G | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3046+295G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125342594 | |||||||
| chr9:125343062 | T | C | 2 | a0001c0001t0002g0106 a0001c0001t0031g0105 |
2 | HG02132.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3046+763T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343062 | |||||||
| chr9:125343195 | T | C | 1 | a0001c0004t0002g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3046+896T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343195 | |||||||
| chr9:125343459 | A | G | 7 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0305 others(4): Show |
7 | HG02056.hp1 NA18942.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.3046+1160A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343459 | |||||||
| chr9:125343464 | T | C | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3046+1165T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343464 | |||||||
| chr9:125343548 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0073 |
2 | HG02071.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3046+1249G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343548 | |||||||
| chr9:125343752 | C | A | 14 | a0001c0001t0005g0306 a0001c0001t0005g0327 a0001c0001t0005g0328 others(11): Show |
14 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.3046+1453C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343752 | |||||||
| chr9:125343820 | G | A | 2 | a0001c0003t0006g0132 a0001c0003t0006g0134 |
2 | HG01167.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3046+1521G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343820 | |||||||
| chr9:125343985 | A | G | 4 | a0001c0001t0002g0071 a0001c0001t0002g0089 a0001c0001t0002g0097 others(1): Show |
4 | HG00438.hp2 NA18978.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046+1686A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343985 | |||||||
| chr9:125344103 | G | C | 34 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(31): Show |
34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.3046+1804G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344103 | |||||||
| chr9:125344201 | T | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0264 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3046+1902T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344201 | |||||||
| chr9:125344206 | A | G | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3046+1907A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344206 | |||||||
| chr9:125344354 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3046+2055T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344354 | |||||||
| chr9:125344408 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3046+2109G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344408 | |||||||
| chr9:125344807 | TA | T | 10 | a0001c0001t0001g0222 a0001c0001t0002g0017 a0001c0001t0002g0055 others(7): Show |
10 | HG00280.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3047-1997delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125344807 | ||||||
| chr9:125344964 | A | G | 10 | a0001c0001t0001g0191 a0001c0001t0001g0268 a0001c0001t0001g0297 others(7): Show |
10 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.3047-1855A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344964 | |||||||
| chr9:125345071 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3047-1748C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345071 | |||||||
| chr9:125345181 | T | C | 2 | a0001c0002t0007g0148 a0001c0002t0007g0169 |
2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.3047-1638T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345181 | |||||||
| chr9:125345226 | G | A | 1 | a0001c0005t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3047-1593G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345226 | |||||||
| chr9:125345427 | C | T | 165 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(162): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3047-1392C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345427 | |||||||
| chr9:125345606 | A | G | 165 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(162): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3047-1213A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345606 | |||||||
| chr9:125345677 | G | A | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3047-1142G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345677 | |||||||
| chr9:125345789 | C | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3047-1030C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345789 | |||||||
| chr9:125345821 | A | G | 1 | a0001c0013t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3047-998A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345821 | |||||||
| chr9:125345825 | A | AAC | 4 | a0001c0001t0005g0306 a0001c0001t0005g0330 a0001c0001t0005g0331 others(1): Show |
4 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.3047-982_3047-981d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125345825 | ||||||
| chr9:125345834 | A | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0229 a0001c0001t0001g0234 |
3 | HG04204.hp2 NA18967.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3047-985A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345834 | |||||||
| chr9:125345866 | A | AGT | 4 | a0001c0001t0002g0056 a0001c0001t0002g0121 a0001c0001t0004g0172 others(1): Show |
4 | HG01099.hp1 HG02257.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047-936_3047-935d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125345866 | ||||||
| chr9:125345883 | G | GTA | 3 | a0001c0001t0001g0258 a0001c0001t0017g0014 a0001c0009t0001g0189 |
3 | HG01243.hp1 HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3047-923_3047-922d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125345883 | ||||||
| chr9:125345885 | A | G | 7 | a0001c0001t0001g0191 a0001c0001t0001g0268 a0001c0001t0001g0322 others(4): Show |
7 | HG00639.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.3047-934A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345885 | |||||||
| chr9:125345913 | G | A | 2 | a0001c0005t0001g0216 a0001c0005t0001g0224 |
2 | HG00280.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.3047-906G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345913 | |||||||
| chr9:125345963 | T | C | 2 | a0003c0007t0001g0300 a0003c0007t0001g0307 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3047-856T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345963 | |||||||
| chr9:125347115 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0252 |
2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.3169+174A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347115 | |||||||
| chr9:125347120 | C | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3169+179C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347120 | |||||||
| chr9:125347148 | C | T | 1 | a0001c0001t0004g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3169+207C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347148 | |||||||
| chr9:125347247 | A | G | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3169+306A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347247 | |||||||
| chr9:125347258 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3169+317G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347258 | |||||||
| chr9:125347454 | G | A | 1 | a0001c0002t0007g0148 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3169+513G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347454 | |||||||
| chr9:125347463 | C | T | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3169+522C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347463 | |||||||
| chr9:125347720 | CA | C | 219 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(216): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.3169+792delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr9 | 125347720 | ||||||
| chr9:125347730 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3169+789A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347730 | |||||||
| chr9:125347733 | A | G | 1 | a0001c0001t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3169+792A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347733 | |||||||
| chr9:125347884 | A | G | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3169+943A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347884 | |||||||
| chr9:125347887 | T | A | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3169+946T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347887 | |||||||
| chr9:125348006 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3169+1065C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348006 | |||||||
| chr9:125348033 | G | GTA | 37 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(34): Show |
37 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.3169+1102_3169+110 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr9 | 125348033 | ||||||
| chr9:125348076 | C | T | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.3169+1135C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348076 | |||||||
| chr9:125348086 | A | G | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3169+1145A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348086 | |||||||
| chr9:125348274 | C | T | 164 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.3170-1116C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348274 | |||||||
| chr9:125348314 | C | T | 1 | a0001c0001t0015g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3170-1076C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348314 | |||||||
| chr9:125348479 | G | A | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 others(4): Show |
7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3170-911G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348479 | |||||||
| chr9:125348497 | T | C | 2 | a0001c0001t0002g0106 a0001c0001t0031g0105 |
2 | HG02132.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3170-893T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348497 | |||||||
| chr9:125348573 | T | C | 231 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(228): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.3170-817T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348573 | |||||||
| chr9:125348605 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3170-785C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348605 | |||||||
| chr9:125348655 | G | A | 2 | a0001c0001t0001g0318 a0001c0001t0001g0320 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3170-735G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348655 | |||||||
| chr9:125348698 | G | A | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3170-692G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348698 | |||||||
| chr9:125349002 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3170-388T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349002 | |||||||
| chr9:125349071 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3170-319T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349071 | |||||||
| chr9:125349147 | G | A | 3 | a0001c0001t0010g0213 a0001c0001t0010g0253 a0001c0001t0010g0263 |
3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3170-243G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349147 | |||||||
| chr9:125349213 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3170-177G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349213 | |||||||
| chr9:125349556 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3299+37G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349556 | |||||||
| chr9:125349724 | C | T | 9 | a0001c0002t0007g0001 a0001c0002t0007g0145 a0001c0002t0007g0150 others(6): Show |
9 | HG00544.hp2 HG01123.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.3299+205C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349724 | |||||||
| chr9:125349804 | G | T | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG00423.hp2 NA18969.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3299+285G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349804 | |||||||
| chr9:125349826 | C | A | 1 | a0001c0001t0001g0259 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3299+307C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349826 | |||||||
| chr9:125349905 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0052 |
2 | HG01099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3299+386G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349905 | |||||||
| chr9:125349961 | A | G | 199 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.3300-334A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349961 | |||||||
| chr9:125350009 | C | T | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3300-286C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125350009 | |||||||
| chr9:125350490 | A | G | 1 | a0001c0002t0007g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3409+86A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 22/27 | chr9 | 125350490 | |||||||
| chr9:125350617 | G | A | 199 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.3410-96G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 22/27 | chr9 | 125350617 | |||||||
| chr9:125351021 | C | T | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3569+149C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351021 | |||||||
| chr9:125351122 | G | A | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3569+250G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351122 | |||||||
| chr9:125351168 | A | G | 4 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.3569+296A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351168 | |||||||
| chr9:125351273 | C | T | 1 | a0001c0002t0003g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3569+401C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351273 | |||||||
| chr9:125351300 | A | C | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3569+428A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351300 | |||||||
| chr9:125351416 | G | T | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3569+544G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351416 | |||||||
| chr9:125351440 | C | T | 32 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0040 others(29): Show |
32 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.3569+568C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351440 | |||||||
| chr9:125351627 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3569+755A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351627 | |||||||
| chr9:125351688 | G | A | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3569+816G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351688 | |||||||
| chr9:125351752 | T | C | 1 | a0001c0003t0004g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3569+880T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351752 | |||||||
| chr9:125351796 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3569+924A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351796 | |||||||
| chr9:125351929 | T | A | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3569+1057T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351929 | |||||||
| chr9:125352067 | C | T | 4 | a0001c0001t0002g0308 a0001c0001t0002g0310 a0001c0001t0002g0313 others(1): Show |
4 | HG02300.hp2 HG02630.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.3569+1195C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352067 | |||||||
| chr9:125352319 | C | T | 6 | a0001c0003t0006g0132 a0001c0003t0006g0134 a0001c0003t0006g0135 others(3): Show |
6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3569+1447C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352319 | |||||||
| chr9:125352441 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3569+1569G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352441 | |||||||
| chr9:125352514 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3569+1642G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352514 | |||||||
| chr9:125352661 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3569+1789T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352661 | |||||||
| chr9:125352723 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3569+1851C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352723 | |||||||
| chr9:125352777 | C | G | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3570-1877C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352777 | |||||||
| chr9:125352871 | C | T | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3570-1783C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352871 | |||||||
| chr9:125352890 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3570-1764C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352890 | |||||||
| chr9:125352919 | T | C | 288 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.3570-1735T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352919 | |||||||
| chr9:125353261 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3570-1393G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353261 | |||||||
| chr9:125353391 | A | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3570-1263A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353391 | |||||||
| chr9:125353404 | C | G | 104 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0001t0001g0192 others(101): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.3570-1250C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353404 | |||||||
| chr9:125353662 | A | G | 123 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0178 others(120): Show |
123 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.3570-992A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353662 | |||||||
| chr9:125353799 | A | G | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3570-855A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353799 | |||||||
| chr9:125353812 | A | G | 5 | a0001c0003t0006g0123 a0001c0003t0006g0124 a0001c0003t0006g0125 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3570-842A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353812 | |||||||
| chr9:125353860 | A | G | 1 | a0001c0001t0008g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3570-794A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353860 | |||||||
| chr9:125353882 | T | G | 1 | a0001c0003t0026g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3570-772T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353882 | |||||||
| chr9:125353966 | A | T | 5 | a0001c0003t0004g0020 a0001c0003t0004g0021 a0001c0003t0004g0130 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3570-688A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353966 | |||||||
| chr9:125353979 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3570-675T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353979 | |||||||
| chr9:125354303 | A | T | 1 | a0001c0001t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3570-351A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354303 | |||||||
| chr9:125354306 | T | G | 1 | a0001c0001t0002g0061 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3570-348T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354306 | |||||||
| chr9:125354538 | A | G | 161 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(158): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.3570-116A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354538 | |||||||
| chr9:125354565 | T | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0264 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3570-89T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354565 | |||||||
| chr9:125355097 | T | G | 2 | a0001c0003t0006g0128 a0001c0003t0026g0129 |
2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3757+256T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355097 | |||||||
| chr9:125355185 | C | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3757+344C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355185 | |||||||
| chr9:125355213 | T | TTCA | 226 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.3757+372_3757+373i others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355213 | |||||||
| chr9:125355215 | G | GGGATTCT others(1): Show |
226 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.3757+374_3757+375i others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355215 | |||||||
| chr9:125355315 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3758-329A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355315 | |||||||
| chr9:125355355 | C | T | 2 | a0001c0002t0003g0146 a0001c0002t0003g0165 |
2 | NA18988.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3758-289C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355355 | |||||||
| chr9:125355866 | T | A | 1 | a0001c0001t0001g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3971+9T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125355866 | |||||||
| chr9:125356067 | T | C | 1 | a0001c0002t0003g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3971+210T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356067 | |||||||
| chr9:125356152 | C | A | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3971+295C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356152 | |||||||
| chr9:125356281 | T | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3971+424T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356281 | |||||||
| chr9:125356351 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3971+494C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356351 | |||||||
| chr9:125356387 | T | G | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3971+530T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356387 | |||||||
| chr9:125356922 | G | T | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3971+1065G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356922 | |||||||
| chr9:125357184 | A | G | 32 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(29): Show |
32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3971+1327A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357184 | |||||||
| chr9:125357187 | C | A | 54 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(51): Show |
54 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.3971+1330C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357187 | |||||||
| chr9:125357194 | C | T | 1 | a0001c0009t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3971+1337C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357194 | |||||||
| chr9:125357300 | C | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0311 a0001c0001t0022g0280 |
3 | HG02698.hp2 HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3971+1443C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357300 | |||||||
| chr9:125357326 | C | T | 1 | a0001c0001t0012g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3971+1469C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357326 | |||||||
| chr9:125357890 | G | C | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3972-1530G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357890 | |||||||
| chr9:125357904 | G | T | 14 | a0001c0001t0002g0071 a0001c0001t0002g0089 a0001c0001t0002g0092 others(11): Show |
14 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.3972-1516G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357904 | |||||||
| chr9:125357984 | A | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3972-1436A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357984 | |||||||
| chr9:125357986 | A | AAC | 12 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.3972-1414_3972-141 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr9 | 125357986 | ||||||
| chr9:125357986 | A | C | 6 | a0001c0001t0001g0248 a0001c0001t0001g0323 a0001c0001t0002g0043 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3972-1434A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357986 | |||||||
| chr9:125357988 | C | A | 10 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0230 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.3972-1432C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357988 | |||||||
| chr9:125358035 | C | G | 1 | a0001c0001t0004g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3972-1385C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358035 | |||||||
| chr9:125358533 | A | T | 1 | a0001c0001t0002g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3972-887A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358533 | |||||||
| chr9:125358539 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3972-881G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358539 | |||||||
| chr9:125358834 | C | G | 3 | a0001c0001t0002g0088 a0001c0001t0012g0102 a0001c0001t0012g0103 |
3 | HG00642.hp1 HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3972-586C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358834 | |||||||
| chr9:125359097 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3972-323C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125359097 | |||||||
| chr9:125359099 | T | C | 3 | a0001c0001t0009g0002 a0001c0001t0009g0003 a0001c0001t0009g0004 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3972-321T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125359099 | |||||||
| chr9:125359313 | A | G | 100 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0191 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3972-107A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125359313 | |||||||
| chr9:125359527 | C | T | 1 | a0001c0013t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4044+35C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359527 | |||||||
| chr9:125359545 | T | C | 1 | a0001c0001t0002g0017 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4044+53T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359545 | |||||||
| chr9:125359574 | G | GGAACTGA others(3): Show |
1 | a0001c0002t0007g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4044+84_4044+93dup others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr9 | 125359574 | ||||||
| chr9:125359687 | A | T | 1 | a0001c0001t0015g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4044+195A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359687 | |||||||
| chr9:125359748 | G | A | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4044+256G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359748 | |||||||
| chr9:125359835 | T | C | 1 | a0001c0016t0037g0171 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4044+343T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359835 | |||||||
| chr9:125359927 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.4044+435A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359927 | |||||||
| chr9:125360041 | A | G | 282 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(279): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.4045-487A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125360041 | |||||||
| chr9:125360316 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4045-212G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125360316 | |||||||
| chr9:125360760 | G | A | 1 | a0001c0001t0008g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4242+35G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125360760 | |||||||
| chr9:125360805 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4242+80A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125360805 | |||||||
| chr9:125361055 | G | A | 156 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(153): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.4242+330G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361055 | |||||||
| chr9:125361277 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4242+552C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361277 | |||||||
| chr9:125361278 | G | A | 1 | a0001c0001t0002g0029 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4242+553G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361278 | |||||||
| chr9:125361341 | T | C | 226 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.4242+616T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361341 | |||||||
| chr9:125361473 | G | A | 34 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(31): Show |
34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.4242+748G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361473 | |||||||
| chr9:125361513 | G | A | 156 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0175 others(153): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.4242+788G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361513 | |||||||
| chr9:125361540 | G | A | 1 | a0001c0001t0017g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4242+815G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361540 | |||||||
| chr9:125361608 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4242+883T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361608 | |||||||
| chr9:125362030 | T | C | 35 | a0001c0001t0016g0053 a0001c0002t0003g0005 a0001c0002t0003g0006 others(32): Show |
35 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.4243-576T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125362030 | |||||||
| chr9:125362373 | A | T | 2 | a0002c0006t0011g0142 a0002c0006t0011g0143 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4243-233A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125362373 | |||||||
| chr9:125362519 | A | T | 90 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0192 others(87): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.4243-87A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125362519 |