Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55093 |
| ensemblid | ENSG00000156795.8 |
| hgncid | 25490 |
| symbol | NTAQ1 |
| name | N-terminal glutamine amidase 1 |
| refseq_nuc | NM_018024.3 |
| refseq_prot | NP_060494.1 |
| ensembl_nuc | ENST00000287387.7 |
| ensembl_prot | ENSP00000287387.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 123416774 |
| end | 123442240 |
| strand | + |
| ver | v1.2 |
| region | chr8:123416774-123442240 |
| region5000 | chr8:123411774-123447240 |
| regionname0 | NTAQ1_chr8_123416774_123442240 |
| regionname5000 | NTAQ1_chr8_123411774_123447240 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 205 | 194 | 56 | 42 | 61 | 12 | 22 | 46 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | MEGNG others(200): Show |
chr8 | 123411774 | 123447240 |
| a0002 | 0/1 | 205 | 170 | 30 | 32 | 84 | 2 | 21 | 61 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | MEGNG others(200): Show |
chr8 | 123411774 | 123447240 |
| a0003 | 0/0 | 205 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | MEGNG others(200): Show |
chr8 | 123411774 | 123447240 |
| a0004 | 0/0 | 203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | MEGNG others(198): Show |
chr8 | 123411774 | 123447240 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 615 | 192 | 56 | 41 | 60 | 12 | 22 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ATGGA others(610): Show |
chr8 | 123411774 | 123447240 | ||
| a0001c0004 | 0/0 | 615 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ATGGA others(610): Show |
chr8 | 123411774 | 123447240 | ||
| a0001c0005 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ATGGA others(610): Show |
chr8 | 123411774 | 123447240 | ||
| a0002c0002 | 0/1 | 615 | 169 | 30 | 32 | 83 | 2 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ATGGA others(610): Show |
chr8 | 123411774 | 123447240 | ||
| a0002c0007 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ATGGA others(610): Show |
chr8 | 123411774 | 123447240 | ||
| a0003c0003 | 0/0 | 615 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ATGGA others(610): Show |
chr8 | 123411774 | 123447240 | ||
| a0004c0006 | 0/0 | 609 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ATGGA others(604): Show |
chr8 | 123411774 | 123447240 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1519 | 179 | 46 | 40 | 60 | 11 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0001t0003 | 0/0 | 1519 | 6 | 5 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0001t0004 | 0/0 | 1519 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0001t0005 | 0/0 | 1519 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0001t0006 | 0/0 | 1519 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0001t0007 | 0/0 | 1519 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0001t0008 | 0/0 | 1519 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0004t0001 | 0/0 | 1519 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0001c0005t0001 | 0/0 | 1519 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0002c0002t0002 | 0/1 | 1519 | 169 | 30 | 32 | 83 | 2 | 21 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0002c0007t0002 | 0/0 | 1519 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0003c0003t0001 | 0/0 | 1519 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1514): Show |
chr8 | 123411774 | 123447240 |
| a0004c0006t0001 | 0/0 | 1513 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | ACTAC others(1508): Show |
chr8 | 123411774 | 123447240 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 4 | 3 | 2 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0004t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0001c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0003 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0004 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0006 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0002c0007t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| a0004c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0109 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0104 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0167 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0179 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0110 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0111 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0165 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0106 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0177 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0172 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0262 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0188 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0120 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0184 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0183 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0178 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0182 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0157 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0101 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0153 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0189 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0185 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0170 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0159 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0173 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0140 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0180 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0168 | AFR | ESN | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0133 | SAS | PJL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0197 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0254 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0225 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0136 | SAS | STU | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0138 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | CHB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18971 | hp2 | a0002 | c0007 | t0002 | g0126 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18997 | hp2 | a0004 | c0006 | t0001 | g0266 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19012 | hp2 | a0001 | c0005 | t0001 | g0260 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0181 | AFR | YRI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | ASW | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0095 | EUR | TSI | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | GIH | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0186 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0141 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0164 | AFR | ACB | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | USA | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | LWK | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0102 | REF | REF | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0044 | REF | REF | NTAQ1_chr8_123411774_123447240 | NTAQ1 | chr8 | 123411774 | 123447240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123416868 | G | A | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.19G>A | p.Ala7Thr | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/6 | 95/1519 | 19/618 | 7/205 | chr8 | 123416868 | |||
| chr8:123427934 | A | G | 1 | a0002 | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
missense_variant | MODERATE | c.94A>G | p.Ile32Val | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/6 | 170/1519 | 94/618 | 32/205 | chr8 | 123427934 | |||
| chr8:123436496 | A | G | 1 | a0002 | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
missense_variant | MODERATE | c.278A>G | p.Asn93Ser | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 354/1519 | 278/618 | 93/205 | chr8 | 123436496 | |||
| chr8:123436564 | T | A | 1 | a0002 | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
missense_variant | MODERATE | c.346T>A | p.Phe116Ile | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 422/1519 | 346/618 | 116/205 | chr8 | 123436564 | |||
| chr8:123437226 | C | T | 1 | a0002 | 169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
missense_variant | MODERATE | c.400C>T | p.Arg134Cys | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/6 | 476/1519 | 400/618 | 134/205 | chr8 | 123437226 | |||
| chr8:123437328 | ACTGGAGG others(13): Show |
A | 1 | a0004 | 1 | NA18997.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.505_508+16delGGAGG others(15): Show |
p.Gly169fs | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/6 | 581/1519 | 505/618 | 169/205 | INFO_REALIGN_3_PRIME | chr8 | 123437328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123427993 | T | C | 1 | a0001c0004 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.153T>C | p.Tyr51Tyr | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/6 | 229/1519 | 153/618 | 51/205 | chr8 | 123427993 | |||
| chr8:123436506 | T | C | 1 | a0001c0005 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.288T>C | p.Tyr96Tyr | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 364/1519 | 288/618 | 96/205 | chr8 | 123436506 | |||
| chr8:123436593 | G | A | 1 | a0002c0007 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.375G>A | p.Gln125Gln | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/6 | 451/1519 | 375/618 | 125/205 | chr8 | 123436593 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123416834 | G | C | 1 | a0001c0001t0005 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/6 | 16 | chr8 | 123416834 | ||||||
| chr8:123441422 | T | C | 2 | a0002c0002t0002 a0002c0007t0002 |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*7T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 7 | chr8 | 123441422 | ||||||
| chr8:123441529 | T | C | 2 | a0001c0001t0006 a0001c0001t0007 |
2 | HG02451.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*114T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 114 | chr8 | 123441529 | ||||||
| chr8:123441559 | A | G | 2 | a0002c0002t0002 a0002c0007t0002 |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*144A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 144 | chr8 | 123441559 | ||||||
| chr8:123441626 | C | T | 1 | a0001c0001t0003 | 6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*211C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 211 | chr8 | 123441626 | ||||||
| chr8:123441687 | C | T | 1 | a0001c0001t0004 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*272C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 272 | chr8 | 123441687 | ||||||
| chr8:123441688 | G | A | 1 | a0001c0001t0006 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 273 | chr8 | 123441688 | ||||||
| chr8:123441739 | T | C | 2 | a0002c0002t0002 a0002c0007t0002 |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*324T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 324 | chr8 | 123441739 | ||||||
| chr8:123441767 | T | C | 2 | a0002c0002t0002 a0002c0007t0002 |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*352T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 352 | chr8 | 123441767 | ||||||
| chr8:123441824 | A | G | 2 | a0001c0001t0006 a0001c0001t0007 |
2 | HG02451.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 409 | chr8 | 123441824 | ||||||
| chr8:123441855 | C | T | 1 | a0001c0001t0008 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 440 | chr8 | 123441855 | ||||||
| chr8:123442235 | A | G | 2 | a0002c0002t0002 a0002c0007t0002 |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*820A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 6/6 | 820 | chr8 | 123442235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:123417010 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.83+78G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417010 | |||||||
| chr8:123417106 | G | C | 1 | a0002c0002t0002g0036 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.83+174G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417106 | |||||||
| chr8:123417155 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(93): Show |
123 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.83+223A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417155 | |||||||
| chr8:123417214 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+282C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417214 | |||||||
| chr8:123417244 | C | G | 26 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(23): Show |
30 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+312C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417244 | |||||||
| chr8:123417250 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(217): Show |
295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.83+318G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417250 | |||||||
| chr8:123417404 | A | C | 1 | a0002c0002t0002g0198 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83+472A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417404 | |||||||
| chr8:123417410 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+478A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417410 | |||||||
| chr8:123417491 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.83+559G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417491 | |||||||
| chr8:123417683 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(219): Show |
297 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.83+751A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417683 | |||||||
| chr8:123417714 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.83+782C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417714 | |||||||
| chr8:123417775 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.83+843G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123417775 | |||||||
| chr8:123418087 | A | C | 1 | a0002c0002t0002g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.83+1155A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418087 | |||||||
| chr8:123418223 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(89): Show |
119 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.83+1291G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418223 | |||||||
| chr8:123418226 | G | GAGGCCGA others(6): Show |
1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+1294_83+1295ins others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418226 | |||||||
| chr8:123418268 | T | G | 1 | a0002c0002t0002g0100 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.83+1336T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418268 | |||||||
| chr8:123418447 | C | CA | 102 | a0001c0001t0001g0037 a0001c0001t0001g0163 a0001c0001t0001g0200 others(99): Show |
142 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.83+1531dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123418447 | ||||||
| chr8:123418447 | CA | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(40): Show |
50 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.83+1531delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123418447 | ||||||
| chr8:123418454 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83+1522A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418454 | |||||||
| chr8:123418457 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+1525A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418457 | |||||||
| chr8:123418460 | A | AT | 11 | a0002c0002t0002g0010 a0002c0002t0002g0014 a0002c0002t0002g0026 others(8): Show |
18 | HG00642.hp1 HG00741.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.83+1528_83+1529ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418460 | |||||||
| chr8:123418460 | A | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0042 others(32): Show |
39 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.83+1528A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418460 | |||||||
| chr8:123418464 | T | A | 1 | a0001c0001t0001g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.83+1532T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418464 | |||||||
| chr8:123418474 | A | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 |
3 | HG01496.hp2 HG02683.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.83+1542A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418474 | |||||||
| chr8:123418760 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+1828T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418760 | |||||||
| chr8:123418838 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+1906A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418838 | |||||||
| chr8:123418842 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+1910C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418842 | |||||||
| chr8:123418871 | A | T | 1 | a0002c0002t0002g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1939A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418871 | |||||||
| chr8:123418873 | G | T | 1 | a0002c0002t0002g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1941G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418873 | |||||||
| chr8:123418874 | A | C | 1 | a0002c0002t0002g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1942A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418874 | |||||||
| chr8:123418876 | G | A | 1 | a0002c0002t0002g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.83+1944G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418876 | |||||||
| chr8:123418878 | G | A | 1 | a0002c0002t0002g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.83+1946G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418878 | |||||||
| chr8:123418920 | C | T | 1 | a0002c0002t0002g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.83+1988C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418920 | |||||||
| chr8:123418978 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2046G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418978 | |||||||
| chr8:123418996 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.83+2064G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123418996 | |||||||
| chr8:123419045 | G | A | 1 | a0002c0002t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.83+2113G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419045 | |||||||
| chr8:123419077 | G | GT | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG00140.hp2 HG01255.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+2145_83+2146ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419077 | |||||||
| chr8:123419078 | G | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(273): Show |
359 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.83+2146G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419078 | |||||||
| chr8:123419079 | GGGTTTTT others(9): Show |
G | 1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2148_83+2163del others(16): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419079 | |||||||
| chr8:123419081 | G | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG00140.hp2 HG01255.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+2149G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419081 | |||||||
| chr8:123419081 | GTTTTTTT others(3): Show |
G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0065 others(8): Show |
13 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.83+2175_83+2184del others(10): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(4): Show |
G | 7 | a0001c0001t0001g0042 a0001c0001t0003g0038 a0001c0001t0003g0039 others(4): Show |
7 | HG01099.hp2 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+2174_83+2184del others(11): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83+2173_83+2184del others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0001g0032 a0002c0002t0002g0116 |
2 | HG01891.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.83+2172_83+2184del others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(7): Show |
G | 34 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0053 others(31): Show |
34 | HG00609.hp1 HG00735.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.83+2171_83+2184del others(14): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(8): Show |
G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(174): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.83+2170_83+2184del others(15): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(9): Show |
G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0276 a0002c0002t0002g0020 others(4): Show |
7 | HG02622.hp1 NA18942.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+2169_83+2184del others(16): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(10): Show |
G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0077 |
2 | HG02056.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.83+2168_83+2184del others(17): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419081 | GTTTTTTT others(11): Show |
G | 25 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0078 others(22): Show |
28 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.83+2167_83+2184del others(18): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419081 | ||||||
| chr8:123419097 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2165T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419097 | |||||||
| chr8:123419098 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2166T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419098 | |||||||
| chr8:123419104 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.83+2172T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419104 | |||||||
| chr8:123419111 | T | C | 8 | a0001c0001t0001g0042 a0001c0001t0003g0038 a0001c0001t0003g0039 others(5): Show |
8 | HG01099.hp2 HG02451.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+2179T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419111 | |||||||
| chr8:123419146 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+2214T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419146 | |||||||
| chr8:123419159 | T | G | 26 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(23): Show |
30 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+2227T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419159 | |||||||
| chr8:123419192 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(209): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.83+2260A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419192 | |||||||
| chr8:123419417 | G | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+2485G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419417 | |||||||
| chr8:123419677 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(259): Show |
344 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.83+2745T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419677 | |||||||
| chr8:123419678 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83+2746G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419678 | |||||||
| chr8:123419684 | A | G | 1 | a0001c0001t0003g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83+2752A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419684 | |||||||
| chr8:123419705 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.83+2773T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419705 | |||||||
| chr8:123419733 | G | GCCCCTCC others(10): Show |
1 | a0001c0001t0001g0205 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.83+2804_83+2805ins others(17): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | ||||||
| chr8:123419733 | G | GCCCGCCC others(13): Show |
2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.83+2804_83+2805ins others(20): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | ||||||
| chr8:123419733 | G | GCCCTCCC others(5): Show |
72 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(69): Show |
93 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.83+2814_83+2825dup others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | ||||||
| chr8:123419733 | G | GCCCTCCC others(9): Show |
23 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
29 | HG00609.hp1 HG00673.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.83+2810_83+2825dup others(16): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | ||||||
| chr8:123419733 | G | GCCCTCCC others(13): Show |
1 | a0001c0001t0001g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.83+2806_83+2825dup others(20): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | ||||||
| chr8:123419733 | G | GCCCTCCC others(17): Show |
2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.83+2802_83+2825dup others(24): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419733 | ||||||
| chr8:123419739 | C | CCTCCCTC others(5): Show |
116 | a0001c0001t0001g0163 a0001c0001t0001g0278 a0002c0002t0002g0002 others(113): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.83+2818_83+2819ins others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419739 | ||||||
| chr8:123419741 | T | TCCCTCCC others(6): Show |
1 | a0002c0002t0002g0103 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.83+2818_83+2819ins others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419741 | ||||||
| chr8:123419747 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.83+2815C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419747 | |||||||
| chr8:123419750 | C | CTCCTCCC others(10): Show |
1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+2818_83+2819ins others(17): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419750 | |||||||
| chr8:123419758 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2826T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419758 | |||||||
| chr8:123419771 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2839T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419771 | |||||||
| chr8:123419773 | T | TTCCC | 4 | a0002c0002t0002g0014 a0002c0002t0002g0175 a0002c0002t0002g0176 others(1): Show |
6 | HG02040.hp2 HG03239.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2857_83+2860dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419773 | ||||||
| chr8:123419773 | T | TTCCCTCC others(1): Show |
202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(199): Show |
275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.83+2853_83+2860dup others(8): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419773 | ||||||
| chr8:123419773 | T | TTCCCTCC others(5): Show |
3 | a0002c0002t0002g0104 a0002c0002t0002g0105 a0002c0002t0002g0106 |
3 | HG00323.hp1 HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.83+2849_83+2860dup others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123419773 | ||||||
| chr8:123419775 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2843C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419775 | |||||||
| chr8:123419777 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.83+2845C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419777 | |||||||
| chr8:123419948 | T | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+3016T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123419948 | |||||||
| chr8:123420004 | A | T | 1 | a0002c0002t0002g0036 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.83+3072A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420004 | |||||||
| chr8:123420060 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+3128T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420060 | |||||||
| chr8:123420061 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.83+3129C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420061 | |||||||
| chr8:123420091 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+3159A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420091 | |||||||
| chr8:123420126 | T | G | 1 | a0002c0002t0002g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.83+3194T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420126 | |||||||
| chr8:123420157 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+3225T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420157 | |||||||
| chr8:123420165 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.83+3233G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420165 | |||||||
| chr8:123420330 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.83+3398C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420330 | |||||||
| chr8:123420344 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+3412C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420344 | |||||||
| chr8:123420457 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+3525A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420457 | |||||||
| chr8:123420490 | A | G | 2 | a0002c0002t0002g0178 a0002c0002t0002g0179 |
2 | HG01167.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.83+3558A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420490 | |||||||
| chr8:123420572 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA18946.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.83+3640G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420572 | |||||||
| chr8:123420590 | C | CTTT | 111 | a0001c0001t0001g0163 a0001c0001t0001g0223 a0001c0001t0001g0224 others(108): Show |
159 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.83+3675_83+3677dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | ||||||
| chr8:123420590 | C | CTTTT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(79): Show |
108 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.83+3674_83+3677dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | ||||||
| chr8:123420590 | C | CTTTTT | 16 | a0001c0001t0001g0035 a0001c0001t0001g0199 a0001c0001t0001g0208 others(13): Show |
17 | HG01192.hp2 HG01515.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.83+3673_83+3677dup others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | ||||||
| chr8:123420590 | CT | C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0062 others(18): Show |
24 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.83+3677delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420590 | ||||||
| chr8:123420663 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(210): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.83+3731A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420663 | |||||||
| chr8:123420785 | T | TTTTA | 7 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0003g0038 others(4): Show |
7 | HG01099.hp2 HG02572.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+3874_83+3877dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123420785 | ||||||
| chr8:123420813 | C | T | 1 | a0002c0002t0002g0024 | 2 | NA19056.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.83+3881C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420813 | |||||||
| chr8:123420841 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.83+3909G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420841 | |||||||
| chr8:123420918 | C | T | 118 | a0001c0001t0001g0163 a0001c0001t0001g0278 a0002c0002t0002g0002 others(115): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+3986C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420918 | |||||||
| chr8:123420976 | G | A | 1 | a0002c0002t0002g0109 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.83+4044G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123420976 | |||||||
| chr8:123421031 | T | C | 118 | a0001c0001t0001g0163 a0001c0001t0001g0278 a0002c0002t0002g0002 others(115): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+4099T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421031 | |||||||
| chr8:123421063 | G | A | 114 | a0001c0001t0001g0163 a0001c0001t0001g0278 a0002c0002t0002g0002 others(111): Show |
161 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.83+4131G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421063 | |||||||
| chr8:123421094 | AT | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(267): Show |
353 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.83+4169delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421094 | ||||||
| chr8:123421103 | A | G | 1 | a0002c0002t0002g0180 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.83+4171A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421103 | |||||||
| chr8:123421106 | C | G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+4174C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421106 | |||||||
| chr8:123421115 | A | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.83+4183A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421115 | |||||||
| chr8:123421136 | T | C | 118 | a0001c0001t0001g0163 a0001c0001t0001g0278 a0002c0002t0002g0002 others(115): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+4204T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421136 | |||||||
| chr8:123421172 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.83+4240C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421172 | |||||||
| chr8:123421185 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.83+4253A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421185 | |||||||
| chr8:123421187 | T | C | 118 | a0001c0001t0001g0163 a0001c0001t0001g0278 a0002c0002t0002g0002 others(115): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.83+4255T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421187 | |||||||
| chr8:123421339 | C | A | 117 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(114): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.83+4407C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421339 | |||||||
| chr8:123421357 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(2): Show |
5 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+4425G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421357 | |||||||
| chr8:123421386 | T | TAAGAATA others(345): Show |
1 | a0002c0002t0002g0014 | 3 | HG02040.hp2 HG03239.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.83+4470_83+4471ins others(352): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421386 | ||||||
| chr8:123421386 | T | TAAGAATA others(346): Show |
1 | a0002c0002t0002g0196 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.83+4470_83+4471ins others(353): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421386 | ||||||
| chr8:123421512 | C | CTTTT | 80 | a0002c0002t0002g0004 a0002c0002t0002g0006 a0002c0002t0002g0007 others(77): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.83+4591_83+4594dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421512 | ||||||
| chr8:123421512 | C | CTTTTT | 28 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(25): Show |
50 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.83+4590_83+4594dup others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421512 | ||||||
| chr8:123421512 | C | CTTTTTT | 7 | a0002c0002t0002g0023 a0002c0002t0002g0108 a0002c0002t0002g0160 others(4): Show |
8 | HG00558.hp2 HG02071.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.83+4589_83+4594dup others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421512 | ||||||
| chr8:123421527 | G | T | 1 | a0002c0002t0002g0143 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.83+4595G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421527 | |||||||
| chr8:123421571 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83+4639C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421571 | |||||||
| chr8:123421577 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83+4645C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421577 | |||||||
| chr8:123421615 | G | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(259): Show |
344 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.83+4683G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421615 | |||||||
| chr8:123421620 | C | T | 2 | a0002c0002t0002g0014 a0002c0002t0002g0196 |
4 | HG02040.hp2 HG03239.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+4688C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421620 | |||||||
| chr8:123421694 | C | CTT | 116 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(113): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.83+4773_83+4774dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421694 | ||||||
| chr8:123421751 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(231): Show |
312 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.83+4819T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421751 | |||||||
| chr8:123421825 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+4893G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421825 | |||||||
| chr8:123421849 | C | CG | 117 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(114): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.83+4919dupG | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421849 | ||||||
| chr8:123421864 | A | AT | 26 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(23): Show |
30 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+4941dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123421864 | ||||||
| chr8:123421872 | T | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0228 a0001c0001t0001g0229 |
4 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+4940T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421872 | |||||||
| chr8:123421886 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.83+4954G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421886 | |||||||
| chr8:123421932 | G | A | 117 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(114): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.83+5000G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421932 | |||||||
| chr8:123421984 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.83+5052T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123421984 | |||||||
| chr8:123422060 | C | T | 117 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(114): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.83+5128C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422060 | |||||||
| chr8:123422077 | A | G | 6 | a0002c0002t0002g0007 a0002c0002t0002g0140 a0002c0002t0002g0141 others(3): Show |
10 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+5145A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422077 | |||||||
| chr8:123422109 | C | CCTGT | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(231): Show |
312 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.83+5179_83+5180ins others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422109 | ||||||
| chr8:123422282 | G | GT | 16 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0062 others(13): Show |
19 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.83+5361dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422282 | ||||||
| chr8:123422282 | G | GTTT | 109 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(106): Show |
157 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.83+5359_83+5361dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422282 | ||||||
| chr8:123422282 | G | GTTTT | 6 | a0002c0002t0002g0103 a0002c0002t0002g0139 a0002c0002t0002g0157 others(3): Show |
6 | HG01884.hp1 HG02683.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+5358_83+5361dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422282 | ||||||
| chr8:123422495 | T | C | 3 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 |
3 | HG01099.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84-5429T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422495 | |||||||
| chr8:123422545 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(55): Show |
77 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.84-5379G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422545 | |||||||
| chr8:123422569 | A | G | 117 | a0001c0001t0001g0278 a0002c0002t0002g0002 a0002c0002t0002g0003 others(114): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.84-5355A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422569 | |||||||
| chr8:123422588 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-5336C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422588 | |||||||
| chr8:123422606 | G | GT | 23 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0037 others(20): Show |
25 | HG00673.hp1 HG01433.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.84-5301dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | ||||||
| chr8:123422606 | G | GTT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0099 a0001c0001t0001g0250 others(2): Show |
6 | HG01884.hp2 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-5302_84-5301dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | ||||||
| chr8:123422606 | G | GTTT | 6 | a0001c0001t0001g0267 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-5303_84-5301dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | ||||||
| chr8:123422606 | G | GTTTTTT | 11 | a0001c0001t0001g0017 a0001c0001t0001g0065 a0001c0001t0001g0066 others(8): Show |
14 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.84-5306_84-5301dup others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | ||||||
| chr8:123422606 | GT | G | 8 | a0001c0001t0001g0223 a0002c0002t0002g0013 a0002c0002t0002g0021 others(5): Show |
11 | HG01071.hp1 HG01071.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.84-5301delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | ||||||
| chr8:123422606 | GTT | G | 109 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
154 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.84-5302_84-5301del others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123422606 | ||||||
| chr8:123422683 | G | A | 1 | a0002c0002t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.84-5241G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422683 | |||||||
| chr8:123422737 | G | T | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.84-5187G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422737 | |||||||
| chr8:123422914 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.84-5010G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123422914 | |||||||
| chr8:123423049 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(110): Show |
144 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.84-4875G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423049 | |||||||
| chr8:123423151 | G | A | 116 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(113): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-4773G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423151 | |||||||
| chr8:123423181 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.84-4743C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423181 | |||||||
| chr8:123423182 | A | C | 1 | a0001c0001t0001g0276 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.84-4742A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423182 | |||||||
| chr8:123423187 | G | A | 118 | a0001c0001t0006g0075 a0001c0001t0007g0074 a0002c0002t0002g0002 others(115): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.84-4737G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423187 | |||||||
| chr8:123423232 | TCTCCCTC others(5): Show |
T | 10 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0003g0038 others(7): Show |
10 | HG01099.hp2 HG02451.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-4675_84-4664del others(12): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423232 | ||||||
| chr8:123423270 | GTCTC | G | 3 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 |
3 | HG01099.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84-4648_84-4645del others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423270 | ||||||
| chr8:123423313 | T | TTC | 262 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(259): Show |
344 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.84-4609_84-4608dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423313 | ||||||
| chr8:123423362 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.84-4562T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423362 | |||||||
| chr8:123423362 | T | TCCTTTCC others(50): Show |
3 | a0002c0002t0002g0110 a0002c0002t0002g0112 a0002c0002t0002g0113 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.84-4506_84-4505ins others(57): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423362 | ||||||
| chr8:123423370 | C | G | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-4554C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423370 | |||||||
| chr8:123423381 | C | CCCTTTCC others(12): Show |
24 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(21): Show |
28 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.84-4522_84-4504dup others(19): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423381 | ||||||
| chr8:123423381 | C | CCCTTTCC others(31): Show |
1 | a0001c0001t0001g0084 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.84-4541_84-4504dup others(38): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423381 | ||||||
| chr8:123423381 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.84-4543C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423381 | |||||||
| chr8:123423435 | TTTTCTTT others(1): Show |
T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(91): Show |
118 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.84-4477_84-4470del others(8): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423435 | ||||||
| chr8:123423475 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0270 |
3 | NA18978.hp2 NA18980.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.84-4449T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423475 | |||||||
| chr8:123423574 | C | T | 115 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(112): Show |
163 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.84-4350C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423574 | |||||||
| chr8:123423612 | G | A | 116 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(113): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-4312G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423612 | |||||||
| chr8:123423629 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0230 |
5 | HG02109.hp2 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-4295C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423629 | |||||||
| chr8:123423651 | C | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-4273C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423651 | |||||||
| chr8:123423765 | A | G | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.84-4159A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423765 | |||||||
| chr8:123423829 | G | A | 119 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(116): Show |
167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.84-4095G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423829 | |||||||
| chr8:123423861 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.84-4063T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423861 | |||||||
| chr8:123423870 | T | TTTA | 119 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(116): Show |
167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.84-4036_84-4034dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123423870 | ||||||
| chr8:123423888 | A | T | 1 | a0001c0001t0007g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.84-4036A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123423888 | |||||||
| chr8:123424027 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.84-3897T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424027 | |||||||
| chr8:123424044 | G | A | 1 | a0002c0002t0002g0191 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.84-3880G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424044 | |||||||
| chr8:123424072 | G | GTT | 32 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0072 others(29): Show |
36 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.84-3835_84-3834dup others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | ||||||
| chr8:123424072 | G | GTTT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(84): Show |
114 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.84-3836_84-3834dup others(3): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | ||||||
| chr8:123424072 | G | GTTTT | 18 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0034 others(15): Show |
21 | HG00558.hp1 HG01192.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.84-3837_84-3834dup others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | ||||||
| chr8:123424072 | G | T | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.84-3852G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424072 | |||||||
| chr8:123424072 | GT | G | 104 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(101): Show |
151 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.84-3834delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424072 | ||||||
| chr8:123424076 | T | C | 1 | a0002c0002t0002g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84-3848T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424076 | |||||||
| chr8:123424089 | T | G | 1 | a0002c0002t0002g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84-3835T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424089 | |||||||
| chr8:123424174 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-3750G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424174 | |||||||
| chr8:123424195 | C | T | 1 | a0001c0001t0003g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.84-3729C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424195 | |||||||
| chr8:123424214 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3710A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424214 | |||||||
| chr8:123424247 | AT | A | 118 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(115): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.84-3664delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424247 | ||||||
| chr8:123424273 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(258): Show |
343 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.84-3651T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424273 | |||||||
| chr8:123424304 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-3620A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424304 | |||||||
| chr8:123424322 | A | G | 25 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(22): Show |
29 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.84-3602A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424322 | |||||||
| chr8:123424399 | C | T | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.84-3525C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424399 | |||||||
| chr8:123424419 | T | A | 1 | a0002c0002t0002g0155 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.84-3505T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424419 | |||||||
| chr8:123424522 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.84-3402G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424522 | |||||||
| chr8:123424570 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-3354C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424570 | |||||||
| chr8:123424602 | AACCTCAG others(24): Show |
A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-3307_84-3277del others(31): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123424602 | ||||||
| chr8:123424642 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-3282T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424642 | |||||||
| chr8:123424696 | C | T | 1 | a0002c0002t0002g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.84-3228C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424696 | |||||||
| chr8:123424775 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3149C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424775 | |||||||
| chr8:123424836 | A | G | 1 | a0002c0002t0002g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.84-3088A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424836 | |||||||
| chr8:123424967 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.84-2957T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123424967 | |||||||
| chr8:123425049 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.84-2875T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425049 | |||||||
| chr8:123425061 | T | C | 1 | a0002c0002t0002g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.84-2863T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425061 | |||||||
| chr8:123425192 | A | G | 1 | a0001c0001t0004g0012 | 3 | HG01891.hp1 HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.84-2732A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425192 | |||||||
| chr8:123425216 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.84-2708C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425216 | |||||||
| chr8:123425248 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-2676C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425248 | |||||||
| chr8:123425271 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.84-2653T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425271 | |||||||
| chr8:123425380 | C | A | 1 | a0001c0001t0001g0030 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.84-2544C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425380 | |||||||
| chr8:123425469 | C | A | 6 | a0002c0002t0002g0007 a0002c0002t0002g0140 a0002c0002t0002g0141 others(3): Show |
10 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-2455C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425469 | |||||||
| chr8:123425470 | A | C | 1 | a0002c0002t0002g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.84-2454A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425470 | |||||||
| chr8:123425471 | C | A | 1 | a0002c0002t0002g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.84-2453C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425471 | |||||||
| chr8:123425471 | CT | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0065 a0001c0001t0001g0223 others(6): Show |
9 | HG02895.hp2 HG02922.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.84-2439delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123425471 | ||||||
| chr8:123425472 | T | C | 1 | a0002c0002t0002g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.84-2452T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425472 | |||||||
| chr8:123425496 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.84-2428A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425496 | |||||||
| chr8:123425560 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-2364G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425560 | |||||||
| chr8:123425708 | G | A | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.84-2216G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425708 | |||||||
| chr8:123425735 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-2189C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425735 | |||||||
| chr8:123425775 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-2149C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425775 | |||||||
| chr8:123425822 | C | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-2102C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425822 | |||||||
| chr8:123425834 | G | A | 1 | a0002c0002t0002g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.84-2090G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123425834 | |||||||
| chr8:123426024 | C | T | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-1900C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426024 | |||||||
| chr8:123426091 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-1833G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426091 | |||||||
| chr8:123426375 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-1549G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426375 | |||||||
| chr8:123426395 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-1529C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426395 | |||||||
| chr8:123426480 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-1444A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426480 | |||||||
| chr8:123426642 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-1282G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426642 | |||||||
| chr8:123426651 | T | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-1273T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426651 | |||||||
| chr8:123426677 | T | C | 1 | a0001c0001t0005g0225 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.84-1247T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426677 | |||||||
| chr8:123426747 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.84-1177A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426747 | |||||||
| chr8:123426785 | C | T | 1 | a0002c0002t0002g0137 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.84-1139C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426785 | |||||||
| chr8:123426786 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-1138A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426786 | |||||||
| chr8:123426926 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-998C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426926 | |||||||
| chr8:123426973 | A | G | 1 | a0002c0002t0002g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.84-951A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426973 | |||||||
| chr8:123426978 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84-946A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123426978 | |||||||
| chr8:123427139 | G | T | 1 | a0002c0002t0002g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.84-785G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427139 | |||||||
| chr8:123427154 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-770G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427154 | |||||||
| chr8:123427217 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.84-707A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427217 | |||||||
| chr8:123427225 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84-699G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427225 | |||||||
| chr8:123427247 | C | CT | 102 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(99): Show |
150 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.84-655dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | ||||||
| chr8:123427247 | C | CTT | 19 | a0002c0002t0002g0019 a0002c0002t0002g0022 a0002c0002t0002g0111 others(16): Show |
21 | HG00544.hp1 HG00741.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.84-656_84-655dupTT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | ||||||
| chr8:123427247 | CT | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0042 others(41): Show |
48 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.84-655delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | ||||||
| chr8:123427247 | CTT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(75): Show |
104 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.84-656_84-655delTT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | ||||||
| chr8:123427247 | CTTT | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0202 a0001c0001t0001g0214 others(3): Show |
7 | HG01928.hp2 HG01975.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-657_84-655delTT others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 123427247 | ||||||
| chr8:123427272 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.84-652G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427272 | |||||||
| chr8:123427351 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.84-573C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427351 | |||||||
| chr8:123427402 | G | A | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.84-522G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427402 | |||||||
| chr8:123427457 | T | C | 8 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0144 others(5): Show |
17 | HG00408.hp2 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.84-467T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427457 | |||||||
| chr8:123427464 | G | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0214 a0001c0001t0001g0217 others(1): Show |
5 | HG00609.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-460G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427464 | |||||||
| chr8:123427475 | T | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-449T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427475 | |||||||
| chr8:123427503 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.84-421C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427503 | |||||||
| chr8:123427578 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.84-346G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427578 | |||||||
| chr8:123427789 | A | G | 1 | a0002c0002t0002g0152 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.84-135A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427789 | |||||||
| chr8:123427880 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.84-44A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | chr8 | 123427880 | |||||||
| chr8:123428086 | TA | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.183+75delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428086 | ||||||
| chr8:123428096 | A | AAAG | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(122): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.183+74_183+76dupAA others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428096 | ||||||
| chr8:123428096 | A | AAG | 131 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0223 others(128): Show |
179 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.183+74_183+75insGA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428096 | ||||||
| chr8:123428096 | A | G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.183+73A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428096 | |||||||
| chr8:123428289 | C | T | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+266C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428289 | |||||||
| chr8:123428307 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01109.hp1 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+284C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428307 | |||||||
| chr8:123428447 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.183+424C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428447 | |||||||
| chr8:123428490 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.183+467G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428490 | |||||||
| chr8:123428578 | G | GT | 119 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(116): Show |
167 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.183+564dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428578 | ||||||
| chr8:123428697 | T | TTCAAGTG others(74): Show |
1 | a0004c0006t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.183+708_183+709ins others(81): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123428697 | ||||||
| chr8:123428822 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.183+799G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428822 | |||||||
| chr8:123428948 | T | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(22): Show |
29 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.183+925T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123428948 | |||||||
| chr8:123429046 | A | G | 1 | a0002c0002t0002g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.184-937A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429046 | |||||||
| chr8:123429048 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.184-935G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429048 | |||||||
| chr8:123429128 | T | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.184-855T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429128 | |||||||
| chr8:123429160 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(269): Show |
355 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.184-823A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429160 | |||||||
| chr8:123429192 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.184-791A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429192 | |||||||
| chr8:123429264 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.184-719A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429264 | |||||||
| chr8:123429369 | T | G | 1 | a0002c0002t0002g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184-614T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429369 | |||||||
| chr8:123429578 | G | C | 1 | a0002c0002t0002g0190 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.184-405G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429578 | |||||||
| chr8:123429593 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.184-390G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429593 | |||||||
| chr8:123429602 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(6): Show |
9 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-381C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429602 | |||||||
| chr8:123429690 | C | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.184-293C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429690 | |||||||
| chr8:123429696 | G | A | 1 | a0002c0002t0002g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.184-287G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429696 | |||||||
| chr8:123429708 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.184-275C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429708 | |||||||
| chr8:123429724 | T | A | 1 | a0004c0006t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.184-259T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429724 | |||||||
| chr8:123429725 | A | T | 1 | a0004c0006t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.184-258A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429725 | |||||||
| chr8:123429768 | T | A | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.184-215T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429768 | |||||||
| chr8:123429769 | A | T | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.184-214A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429769 | |||||||
| chr8:123429792 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.184-191A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429792 | |||||||
| chr8:123429874 | TGTCTCAA others(20): Show |
T | 42 | a0002c0002t0002g0004 a0002c0002t0002g0009 a0002c0002t0002g0010 others(39): Show |
59 | HG00280.hp2 HG00642.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.184-90_184-64delAA others(25): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429874 | ||||||
| chr8:123429879 | C | CA | 76 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0077 others(73): Show |
104 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.184-86dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429879 | ||||||
| chr8:123429879 | C | CAA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(91): Show |
119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.184-87_184-86dupAA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429879 | ||||||
| chr8:123429879 | C | CAAA | 12 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0201 others(9): Show |
12 | HG01109.hp1 HG01433.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-88_184-86dupAA others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 123429879 | ||||||
| chr8:123429941 | T | G | 11 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0103 others(8): Show |
20 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.184-42T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429941 | |||||||
| chr8:123429947 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.184-36A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 2/5 | chr8 | 123429947 | |||||||
| chr8:123430360 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+327G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430360 | |||||||
| chr8:123430362 | C | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+329C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430362 | |||||||
| chr8:123430369 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.234+336C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430369 | |||||||
| chr8:123430412 | T | G | 1 | a0004c0006t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.234+379T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430412 | |||||||
| chr8:123430413 | G | T | 1 | a0004c0006t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.234+380G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430413 | |||||||
| chr8:123430462 | C | T | 1 | a0002c0002t0002g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.234+429C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430462 | |||||||
| chr8:123430594 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.234+561A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430594 | |||||||
| chr8:123430738 | T | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+705T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430738 | |||||||
| chr8:123430787 | T | C | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+754T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430787 | |||||||
| chr8:123430809 | T | C | 1 | a0002c0002t0002g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.234+776T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123430809 | |||||||
| chr8:123431024 | C | A | 1 | a0002c0002t0002g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.234+991C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431024 | |||||||
| chr8:123431053 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+1020T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431053 | |||||||
| chr8:123431066 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+1033G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431066 | |||||||
| chr8:123431179 | G | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.234+1146G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431179 | |||||||
| chr8:123431195 | G | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+1162G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431195 | |||||||
| chr8:123431241 | G | A | 9 | a0001c0001t0001g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(6): Show |
9 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+1208G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431241 | |||||||
| chr8:123431268 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(6): Show |
9 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.234+1235C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431268 | |||||||
| chr8:123431293 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0077 others(22): Show |
29 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+1260C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431293 | |||||||
| chr8:123431325 | G | A | 4 | a0002c0002t0002g0124 a0002c0002t0002g0125 a0002c0002t0002g0154 others(1): Show |
4 | HG02071.hp2 NA18971.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+1292G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431325 | |||||||
| chr8:123431337 | CA | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0079 others(3): Show |
6 | HG01099.hp2 HG01175.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+1324delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | ||||||
| chr8:123431337 | CAA | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0037 others(31): Show |
38 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.234+1323_234+1324d others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | ||||||
| chr8:123431337 | CAAA | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(84): Show |
115 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.234+1322_234+1324d others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | ||||||
| chr8:123431337 | CAAAA | C | 135 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0064 others(132): Show |
185 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.234+1321_234+1324d others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123431337 | ||||||
| chr8:123431364 | T | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+1331T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431364 | |||||||
| chr8:123431381 | C | T | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+1348C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431381 | |||||||
| chr8:123431419 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+1386G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431419 | |||||||
| chr8:123431429 | C | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+1396C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431429 | |||||||
| chr8:123431439 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.234+1406G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431439 | |||||||
| chr8:123431574 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.234+1541C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431574 | |||||||
| chr8:123431593 | T | C | 1 | a0002c0002t0002g0143 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.234+1560T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431593 | |||||||
| chr8:123431773 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+1740G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431773 | |||||||
| chr8:123431774 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+1741C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431774 | |||||||
| chr8:123431784 | G | A | 1 | a0002c0002t0002g0164 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234+1751G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431784 | |||||||
| chr8:123431794 | G | C | 1 | a0004c0006t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.234+1761G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431794 | |||||||
| chr8:123431881 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.234+1848G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431881 | |||||||
| chr8:123431937 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.234+1904G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123431937 | |||||||
| chr8:123432237 | T | G | 4 | a0001c0001t0001g0211 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG00673.hp1 NA18981.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+2204T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432237 | |||||||
| chr8:123432256 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2223A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432256 | |||||||
| chr8:123432344 | C | G | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+2311C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432344 | |||||||
| chr8:123432375 | C | T | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+2342C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432375 | |||||||
| chr8:123432496 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2463G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432496 | |||||||
| chr8:123432512 | G | A | 120 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(117): Show |
168 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.234+2479G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432512 | |||||||
| chr8:123432599 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2566T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432599 | |||||||
| chr8:123432630 | A | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.234+2597A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432630 | |||||||
| chr8:123432678 | T | C | 1 | a0002c0002t0002g0127 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.234+2645T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432678 | |||||||
| chr8:123432687 | A | AT | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.234+2664dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123432687 | ||||||
| chr8:123432719 | G | A | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+2686G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432719 | |||||||
| chr8:123432776 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2743G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432776 | |||||||
| chr8:123432834 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2801C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432834 | |||||||
| chr8:123432876 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.234+2843T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432876 | |||||||
| chr8:123432895 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2862A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432895 | |||||||
| chr8:123432905 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234+2872C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123432905 | |||||||
| chr8:123433029 | C | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.234+2996C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433029 | |||||||
| chr8:123433241 | G | T | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+3208G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433241 | |||||||
| chr8:123433493 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.235-2960G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433493 | |||||||
| chr8:123433519 | C | T | 27 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0014 others(24): Show |
47 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.235-2934C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433519 | |||||||
| chr8:123433557 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0259 |
3 | HG02055.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235-2896C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433557 | |||||||
| chr8:123433604 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.235-2849T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433604 | |||||||
| chr8:123433609 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(90): Show |
120 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.235-2844G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123433609 | |||||||
| chr8:123433925 | A | AT | 23 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0078 others(20): Show |
27 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.235-2514dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123433925 | ||||||
| chr8:123433925 | A | ATT | 119 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0002c0002t0002g0002 others(116): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.235-2515_235-2514d others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123433925 | ||||||
| chr8:123433925 | AT | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(108): Show |
141 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.235-2514delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123433925 | ||||||
| chr8:123434038 | G | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.235-2415G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434038 | |||||||
| chr8:123434129 | G | GCTCCTGC others(10): Show |
1 | a0001c0001t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.235-2297_235-2281d others(19): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123434129 | ||||||
| chr8:123434129 | GCTCCTGC others(10): Show |
G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0273 |
3 | HG03942.hp1 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.235-2297_235-2281d others(19): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123434129 | ||||||
| chr8:123434205 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.235-2248G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434205 | |||||||
| chr8:123434316 | T | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-2137T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434316 | |||||||
| chr8:123434352 | C | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0237 |
2 | HG01123.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.235-2101C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434352 | |||||||
| chr8:123434556 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-1897T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434556 | |||||||
| chr8:123434557 | G | A | 1 | a0002c0002t0002g0150 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.235-1896G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434557 | |||||||
| chr8:123434573 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-1880T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434573 | |||||||
| chr8:123434579 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.235-1874T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434579 | |||||||
| chr8:123434632 | C | G | 1 | a0002c0002t0002g0152 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.235-1821C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434632 | |||||||
| chr8:123434661 | G | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-1792G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434661 | |||||||
| chr8:123434690 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-1763A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434690 | |||||||
| chr8:123434697 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-1756G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434697 | |||||||
| chr8:123434714 | G | A | 1 | a0002c0002t0002g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235-1739G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434714 | |||||||
| chr8:123434829 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-1624T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123434829 | |||||||
| chr8:123435016 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.235-1437A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435016 | |||||||
| chr8:123435068 | A | G | 1 | a0001c0001t0003g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235-1385A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435068 | |||||||
| chr8:123435092 | T | C | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-1361T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435092 | |||||||
| chr8:123435122 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-1331T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435122 | |||||||
| chr8:123435224 | C | T | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.235-1229C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435224 | |||||||
| chr8:123435243 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.235-1210C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435243 | |||||||
| chr8:123435357 | CT | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0215 a0001c0001t0001g0219 others(2): Show |
5 | HG00323.hp1 HG00323.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-1089delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123435357 | ||||||
| chr8:123435449 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235-1004C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435449 | |||||||
| chr8:123435546 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.235-907T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435546 | |||||||
| chr8:123435559 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-894A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435559 | |||||||
| chr8:123435749 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0245 a0001c0001t0001g0276 |
3 | NA18747.hp1 NA18974.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.235-704C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435749 | |||||||
| chr8:123435782 | G | A | 52 | a0002c0002t0002g0004 a0002c0002t0002g0009 a0002c0002t0002g0010 others(49): Show |
69 | HG00280.hp2 HG00642.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.235-671G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435782 | |||||||
| chr8:123435870 | T | A | 1 | a0004c0006t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.235-583T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435870 | |||||||
| chr8:123435881 | T | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-572T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435881 | |||||||
| chr8:123435948 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-505G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435948 | |||||||
| chr8:123435948 | G | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.235-505G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123435948 | |||||||
| chr8:123436102 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-351G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436102 | |||||||
| chr8:123436123 | C | T | 1 | a0001c0001t0003g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235-330C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436123 | |||||||
| chr8:123436169 | C | CA | 45 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(42): Show |
50 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.235-263dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123436169 | ||||||
| chr8:123436169 | CA | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(58): Show |
80 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.235-263delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123436169 | ||||||
| chr8:123436169 | CAA | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(31): Show |
42 | HG00408.hp1 HG00609.hp1 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.235-264_235-263del others(2): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 123436169 | ||||||
| chr8:123436190 | A | T | 1 | a0001c0001t0001g0278 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.235-263A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436190 | |||||||
| chr8:123436212 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-241A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436212 | |||||||
| chr8:123436273 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.235-180C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436273 | |||||||
| chr8:123436285 | A | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-168A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436285 | |||||||
| chr8:123436307 | G | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(87): Show |
117 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.235-146G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436307 | |||||||
| chr8:123436436 | G | T | 1 | a0002c0002t0002g0101 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.235-17G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436436 | |||||||
| chr8:123436449 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
splice_region_variant&intron_variant | LOW | c.235-4T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 3/5 | chr8 | 123436449 | |||||||
| chr8:123436667 | CTT | C | 120 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(117): Show |
168 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.383+76_383+77delTT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 123436667 | ||||||
| chr8:123436707 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
350 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.383+106A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123436707 | |||||||
| chr8:123436840 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(272): Show |
358 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.383+239G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123436840 | |||||||
| chr8:123436953 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.384-257C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123436953 | |||||||
| chr8:123437028 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.384-182G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437028 | |||||||
| chr8:123437031 | G | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.384-179G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437031 | |||||||
| chr8:123437095 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.384-115C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437095 | |||||||
| chr8:123437103 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-107C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437103 | |||||||
| chr8:123437168 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.384-42A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 4/5 | chr8 | 123437168 | |||||||
| chr8:123437432 | T | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+98T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437432 | |||||||
| chr8:123437472 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+138G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437472 | |||||||
| chr8:123437478 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.508+144C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437478 | |||||||
| chr8:123437502 | C | G | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+168C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437502 | |||||||
| chr8:123437594 | T | C | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.508+260T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437594 | |||||||
| chr8:123437595 | A | C | 1 | a0002c0002t0002g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.508+261A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437595 | |||||||
| chr8:123437696 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.508+362C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437696 | |||||||
| chr8:123437702 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(102): Show |
135 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.508+383delA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123437702 | ||||||
| chr8:123437707 | AAAAAAAA others(4): Show |
A | 117 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(114): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.508+380_508+390del others(11): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123437707 | ||||||
| chr8:123437708 | AAAAAAAA others(3): Show |
A | 4 | a0002c0002t0002g0140 a0002c0002t0002g0153 a0002c0002t0002g0154 others(1): Show |
4 | HG02071.hp2 HG02738.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+381_508+390del others(10): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123437708 | ||||||
| chr8:123437711 | A | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(36): Show |
46 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.508+377A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437711 | |||||||
| chr8:123437859 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.508+525A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437859 | |||||||
| chr8:123437876 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+542C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437876 | |||||||
| chr8:123437938 | C | T | 4 | a0002c0002t0002g0021 a0002c0002t0002g0114 a0002c0002t0002g0138 others(1): Show |
5 | HG01071.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+604C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437938 | |||||||
| chr8:123437945 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+611T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123437945 | |||||||
| chr8:123438023 | A | T | 1 | a0002c0002t0002g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508+689A>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438023 | |||||||
| chr8:123438087 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.508+753C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438087 | |||||||
| chr8:123438124 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+790G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438124 | |||||||
| chr8:123438163 | T | C | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.508+829T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438163 | |||||||
| chr8:123438191 | A | G | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.508+857A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438191 | |||||||
| chr8:123438391 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+1057T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438391 | |||||||
| chr8:123438448 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.508+1114G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438448 | |||||||
| chr8:123438477 | G | A | 6 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(3): Show |
6 | HG01099.hp2 HG03041.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+1143G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438477 | |||||||
| chr8:123438485 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+1151G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438485 | |||||||
| chr8:123438603 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.508+1269C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438603 | |||||||
| chr8:123438672 | C | CA | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(212): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.508+1351dupA | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123438672 | ||||||
| chr8:123438723 | T | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.508+1389T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438723 | |||||||
| chr8:123438764 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+1430G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438764 | |||||||
| chr8:123438789 | C | G | 1 | a0001c0001t0006g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.508+1455C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438789 | |||||||
| chr8:123438842 | A | C | 1 | a0002c0002t0002g0154 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.508+1508A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438842 | |||||||
| chr8:123438905 | C | T | 4 | a0002c0002t0002g0021 a0002c0002t0002g0114 a0002c0002t0002g0138 others(1): Show |
5 | HG01071.hp2 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+1571C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123438905 | |||||||
| chr8:123439028 | C | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.508+1694C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439028 | |||||||
| chr8:123439113 | G | A | 1 | a0002c0002t0002g0127 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.508+1779G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439113 | |||||||
| chr8:123439158 | G | T | 32 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(29): Show |
40 | HG00408.hp1 HG00609.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.508+1824G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439158 | |||||||
| chr8:123439271 | T | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.508+1937T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439271 | |||||||
| chr8:123439345 | G | GT | 109 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0098 others(106): Show |
156 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.509-1946dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439345 | ||||||
| chr8:123439345 | G | GTT | 10 | a0002c0002t0002g0116 a0002c0002t0002g0129 a0002c0002t0002g0134 others(7): Show |
10 | HG01952.hp1 HG02015.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.509-1947_509-1946d others(4): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439345 | ||||||
| chr8:123439345 | GT | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(106): Show |
139 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.509-1946delT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439345 | ||||||
| chr8:123439359 | T | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
14 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-1947T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439359 | |||||||
| chr8:123439361 | G | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-1945G>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439361 | |||||||
| chr8:123439365 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(91): Show |
123 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.509-1941C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439365 | |||||||
| chr8:123439428 | C | T | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.509-1878C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439428 | |||||||
| chr8:123439435 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(91): Show |
123 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.509-1871C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439435 | |||||||
| chr8:123439536 | T | TG | 3 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0052 |
4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-1766dupG | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123439536 | ||||||
| chr8:123439547 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-1759C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439547 | |||||||
| chr8:123439621 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509-1685C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439621 | |||||||
| chr8:123439635 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-1671C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439635 | |||||||
| chr8:123439636 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-1670G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439636 | |||||||
| chr8:123439698 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
315 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.509-1608T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439698 | |||||||
| chr8:123439707 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0163 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509-1599C>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439707 | |||||||
| chr8:123439748 | C | G | 1 | a0002c0007t0002g0126 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.509-1558C>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123439748 | |||||||
| chr8:123440106 | G | C | 1 | a0002c0002t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509-1200G>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440106 | |||||||
| chr8:123440127 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509-1179C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440127 | |||||||
| chr8:123440146 | C | CT | 14 | a0001c0001t0001g0017 a0001c0001t0001g0054 a0001c0001t0001g0057 others(11): Show |
15 | HG00639.hp2 HG00735.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.509-1133dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440146 | C | CTTT | 15 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0070 others(12): Show |
18 | HG00323.hp2 HG01099.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.509-1135_509-1133d others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440146 | C | CTTTT | 10 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
11 | HG00140.hp1 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-1136_509-1133d others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440146 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0003g0097 a0001c0001t0006g0075 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509-1143_509-1133d others(13): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440146 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0041 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.509-1148_509-1133d others(18): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440146 | CTTT | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0230 a0001c0001t0001g0256 others(5): Show |
11 | HG02015.hp1 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-1135_509-1133d others(5): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440146 | CTTTT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0028 others(85): Show |
112 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.509-1136_509-1133d others(6): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440146 | CTTTTT | C | 114 | a0001c0001t0001g0015 a0001c0001t0001g0200 a0001c0001t0001g0209 others(111): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.509-1137_509-1133d others(7): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440146 | ||||||
| chr8:123440190 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-1116C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440190 | |||||||
| chr8:123440258 | C | T | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.509-1048C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440258 | |||||||
| chr8:123440338 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.509-968T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440338 | |||||||
| chr8:123440392 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.509-914G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440392 | |||||||
| chr8:123440463 | G | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-843G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440463 | |||||||
| chr8:123440466 | T | C | 2 | a0001c0001t0006g0075 a0001c0001t0007g0074 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.509-840T>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440466 | |||||||
| chr8:123440481 | T | G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0273 |
3 | HG03942.hp1 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.509-825T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440481 | |||||||
| chr8:123440502 | C | CT | 117 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0094 others(114): Show |
165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.509-788dupT | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440502 | ||||||
| chr8:123440504 | T | TC | 6 | a0002c0002t0002g0049 a0002c0002t0002g0055 a0002c0002t0002g0110 others(3): Show |
6 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.509-802_509-801ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440504 | |||||||
| chr8:123440647 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.509-659G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440647 | |||||||
| chr8:123440743 | T | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
14 | HG00639.hp2 HG00735.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-563T>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440743 | |||||||
| chr8:123440783 | G | A | 3 | a0002c0002t0002g0134 a0002c0002t0002g0135 a0002c0002t0002g0139 |
3 | NA18997.hp1 NA19054.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.509-523G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440783 | |||||||
| chr8:123440789 | A | C | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-517A>C | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440789 | |||||||
| chr8:123440836 | C | T | 8 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(5): Show |
8 | HG01099.hp2 HG02451.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.509-470C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440836 | |||||||
| chr8:123440963 | C | T | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-343C>T | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123440963 | |||||||
| chr8:123440990 | TCATGAAG others(8): Show |
T | 1 | a0001c0001t0007g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.509-312_509-298del others(15): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 123440990 | ||||||
| chr8:123441040 | C | CA | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.509-266_509-265ins others(1): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441040 | |||||||
| chr8:123441067 | G | A | 1 | a0002c0002t0002g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.509-239G>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441067 | |||||||
| chr8:123441160 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509-146A>G | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441160 | |||||||
| chr8:123441303 | T | A | 121 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(118): Show |
169 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
splice_region_variant&intron_variant | LOW | c.509-3T>A | NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 5/5 | chr8 | 123441303 |