Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7299 |
| ensemblid | ENSG00000077498.9 |
| hgncid | 12442 |
| symbol | TYR |
| name | tyrosinase |
| refseq_nuc | NM_000372.5 |
| refseq_prot | NP_000363.1 |
| ensembl_nuc | ENST00000263321.6 |
| ensembl_prot | ENSP00000263321.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 89177875 |
| end | 89295759 |
| strand | + |
| ver | v1.2 |
| region | chr11:89177875-89295759 |
| region5000 | chr11:89172875-89300759 |
| regionname0 | TYR_chr11_89177875_89295759 |
| regionname5000 | TYR_chr11_89172875_89300759 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 529 | 275 | 84 | 29 | 125 | 7 | 29 | 100 | TYR_chr11_89172875_89300759 | TYR | MLLAV others(524): Show |
chr11 | 89172875 | 89300759 |
| a0002 | 0/1 | 529 | 16 | 4 | 8 | 1 | 1 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | MLLAV others(524): Show |
chr11 | 89172875 | 89300759 |
| a0003 | 0/0 | 529 | 12 | 0 | 5 | 0 | 3 | 4 | 0 | TYR_chr11_89172875_89300759 | TYR | MLLAV others(524): Show |
chr11 | 89172875 | 89300759 |
| a0004 | 0/0 | 529 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | MLLAV others(524): Show |
chr11 | 89172875 | 89300759 |
| a0005 | 0/0 | 529 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | MLLAV others(524): Show |
chr11 | 89172875 | 89300759 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1587 | 266 | 76 | 29 | 124 | 7 | 29 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 | ||
| a0001c0004 | 0/0 | 1587 | 6 | 6 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 | ||
| a0001c0006 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 | ||
| a0001c0008 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 | ||
| a0002c0002 | 0/1 | 1587 | 16 | 4 | 8 | 1 | 1 | 1 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 | ||
| a0003c0003 | 0/0 | 1587 | 12 | 0 | 5 | 0 | 3 | 4 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 | ||
| a0004c0005 | 0/0 | 1587 | 2 | 0 | 1 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 | ||
| a0005c0007 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ATGCT others(1582): Show |
chr11 | 89172875 | 89300759 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2062 | 265 | 76 | 29 | 123 | 7 | 29 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0001c0001t0002 | 0/0 | 2062 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0001c0004t0001 | 0/0 | 2062 | 6 | 6 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0001c0006t0001 | 0/0 | 2062 | 2 | 2 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0001c0008t0001 | 0/0 | 2062 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0002c0002t0001 | 0/1 | 2062 | 16 | 4 | 8 | 1 | 1 | 1 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0003c0003t0001 | 0/0 | 2062 | 12 | 0 | 5 | 0 | 3 | 4 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0004c0005t0001 | 0/0 | 2062 | 2 | 0 | 1 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| a0005c0007t0001 | 0/0 | 2062 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | ACTGT others(2057): Show |
chr11 | 89172875 | 89300759 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0006t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0006t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0001c0008t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0003c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0004c0005t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0004c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| a0005c0007t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0020 | EUR | GBR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0190 | EUR | FIN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0023 | EUR | FIN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | CHS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01106 | hp1 | a0004 | c0005 | t0001 | g0175 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0017 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0019 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01257 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01515 | hp1 | a0004 | c0005 | t0001 | g0189 | EUR | IBS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0018 | EUR | IBS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01975 | hp1 | a0005 | c0007 | t0001 | g0048 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0022 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0287 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0083 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0185 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0283 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0284 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0021 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0285 | AFR | YRI | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18968 | hp1 | a0001 | c0008 | t0001 | g0008 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ASW | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0139 | AFR | ASW | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02486 | hp1 | a0001 | c0004 | t0001 | g0288 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0082 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | USA | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | USA | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0286 | AFR | USA | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0140 | REF | REF | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0167 | REF | REF | TYR_chr11_89172875_89300759 | TYR | chr11 | 89172875 | 89300759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89178483 | T | C | 1 | a0005 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.530T>C | p.Val177Ala | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/5 | 609/2062 | 530/1590 | 177/529 | chr11 | 89178483 | |||
| chr11:89178528 | C | A | 2 | a0002 a0004 |
17 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(14): Show |
missense_variant | MODERATE | c.575C>A | p.Ser192Tyr | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/5 | 654/2062 | 575/1590 | 192/529 | chr11 | 89178528 | |||
| chr11:89284793 | G | A | 2 | a0003 a0004 |
14 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(11): Show |
missense_variant | MODERATE | c.1205G>A | p.Arg402Gln | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/5 | 1284/2062 | 1205/1590 | 402/529 | chr11 | 89284793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89178001 | C | T | 1 | a0001c0008 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.48C>T | p.Ser16Ser | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/5 | 127/2062 | 48/1590 | 16/529 | chr11 | 89178001 | |||
| chr11:89178067 | G | A | 1 | a0001c0004 | 6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
synonymous_variant | LOW | c.114G>A | p.Pro38Pro | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/5 | 193/2062 | 114/1590 | 38/529 | chr11 | 89178067 | |||
| chr11:89178131 | C | T | 1 | a0001c0004 | 6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
synonymous_variant | LOW | c.178C>T | p.Leu60Leu | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/5 | 257/2062 | 178/1590 | 60/529 | chr11 | 89178131 | |||
| chr11:89191217 | T | C | 1 | a0001c0006 | 2 | HG02630.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.835T>C | p.Leu279Leu | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/5 | 914/2062 | 835/1590 | 279/529 | chr11 | 89191217 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89295556 | C | G | 1 | a0001c0001t0002 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*190C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 5/5 | 190 | chr11 | 89295556 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89178875 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.819+103C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89178875 | |||||||
| chr11:89179022 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
63 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.819+250T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89179022 | |||||||
| chr11:89179040 | A | T | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+268A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89179040 | |||||||
| chr11:89179260 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.819+488G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89179260 | |||||||
| chr11:89179488 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.819+716T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89179488 | |||||||
| chr11:89179523 | T | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0070 others(46): Show |
50 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(47): Show |
intron_variant | MODIFIER | c.819+751T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89179523 | |||||||
| chr11:89179552 | CA | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(59): Show |
65 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.819+790delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 89179552 | ||||||
| chr11:89179985 | A | G | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+1213A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89179985 | |||||||
| chr11:89179995 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.819+1223T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89179995 | |||||||
| chr11:89180101 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.819+1329T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180101 | |||||||
| chr11:89180111 | T | A | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0118 others(7): Show |
10 | HG01243.hp2 HG02615.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.819+1339T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180111 | |||||||
| chr11:89180277 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.819+1505A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180277 | |||||||
| chr11:89180477 | A | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+1705A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180477 | |||||||
| chr11:89180495 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.819+1723A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180495 | |||||||
| chr11:89180553 | G | GA | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0004t0001g0283 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.819+1793dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 89180553 | ||||||
| chr11:89180567 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.819+1795T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180567 | |||||||
| chr11:89180569 | T | G | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+1797T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180569 | |||||||
| chr11:89180710 | G | A | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG01243.hp1 HG02486.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+1938G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180710 | |||||||
| chr11:89180734 | A | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+1962A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89180734 | |||||||
| chr11:89181087 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.819+2315A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181087 | |||||||
| chr11:89181100 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.819+2328C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181100 | |||||||
| chr11:89181163 | T | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(157): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.819+2391T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181163 | |||||||
| chr11:89181247 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(56): Show |
62 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.819+2475C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181247 | |||||||
| chr11:89181364 | G | T | 1 | a0002c0002t0001g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.819+2592G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181364 | |||||||
| chr11:89181399 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.819+2627T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181399 | |||||||
| chr11:89181445 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.819+2673A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181445 | |||||||
| chr11:89181501 | C | G | 1 | a0001c0001t0001g0065 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.819+2729C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181501 | |||||||
| chr11:89181858 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.819+3086G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89181858 | |||||||
| chr11:89182060 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.819+3288G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182060 | |||||||
| chr11:89182182 | A | G | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+3410A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182182 | |||||||
| chr11:89182280 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+3508G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182280 | |||||||
| chr11:89182323 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+3551G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182323 | |||||||
| chr11:89182402 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(155): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.819+3630A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182402 | |||||||
| chr11:89182443 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.819+3671G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182443 | |||||||
| chr11:89182563 | A | G | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | HG02615.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.819+3791A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182563 | |||||||
| chr11:89182564 | T | C | 1 | a0001c0004t0001g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.819+3792T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182564 | |||||||
| chr11:89182696 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.819+3924T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182696 | |||||||
| chr11:89182730 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02165.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.819+3958G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182730 | |||||||
| chr11:89182872 | GA | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(153): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.819+4106delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 89182872 | ||||||
| chr11:89182895 | C | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(79): Show |
84 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.819+4123C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182895 | |||||||
| chr11:89182917 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.819+4145G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89182917 | |||||||
| chr11:89183015 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.819+4243C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183015 | |||||||
| chr11:89183090 | T | C | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+4318T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183090 | |||||||
| chr11:89183094 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+4322T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183094 | |||||||
| chr11:89183325 | C | T | 8 | a0001c0001t0001g0233 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.819+4553C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183325 | |||||||
| chr11:89183355 | C | A | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.819+4583C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183355 | |||||||
| chr11:89183455 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.819+4683A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183455 | |||||||
| chr11:89183478 | G | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(72): Show |
77 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(74): Show |
intron_variant | MODIFIER | c.819+4706G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183478 | |||||||
| chr11:89183884 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.819+5112C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183884 | |||||||
| chr11:89183942 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01243.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+5170C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183942 | |||||||
| chr11:89183943 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.819+5171G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183943 | |||||||
| chr11:89183962 | A | G | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+5190A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89183962 | |||||||
| chr11:89184027 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.819+5255G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184027 | |||||||
| chr11:89184206 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.819+5434C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184206 | |||||||
| chr11:89184246 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.819+5474T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184246 | |||||||
| chr11:89184293 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.819+5521C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184293 | |||||||
| chr11:89184443 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.819+5671T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184443 | |||||||
| chr11:89184454 | C | T | 8 | a0001c0001t0001g0233 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.819+5682C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184454 | |||||||
| chr11:89184468 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.819+5696C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184468 | |||||||
| chr11:89184492 | T | C | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+5720T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184492 | |||||||
| chr11:89184616 | C | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(79): Show |
84 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.819+5844C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184616 | |||||||
| chr11:89184802 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.819+6030C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184802 | |||||||
| chr11:89184884 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.819+6112T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184884 | |||||||
| chr11:89184916 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.819+6144T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89184916 | |||||||
| chr11:89185032 | T | C | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-6170T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185032 | |||||||
| chr11:89185243 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.820-5959T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185243 | |||||||
| chr11:89185346 | A | G | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.820-5856A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185346 | |||||||
| chr11:89185521 | G | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.820-5681G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185521 | |||||||
| chr11:89185533 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-5669G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185533 | |||||||
| chr11:89185575 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.820-5627T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185575 | |||||||
| chr11:89185655 | C | T | 7 | a0001c0001t0001g0276 a0001c0004t0001g0283 a0001c0004t0001g0284 others(4): Show |
7 | HG01346.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-5547C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185655 | |||||||
| chr11:89185721 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.820-5481G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185721 | |||||||
| chr11:89185785 | T | C | 1 | a0002c0002t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.820-5417T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185785 | |||||||
| chr11:89185860 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.820-5342C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185860 | |||||||
| chr11:89185886 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.820-5316T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185886 | |||||||
| chr11:89185899 | C | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(86): Show |
91 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(88): Show |
intron_variant | MODIFIER | c.820-5303C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185899 | |||||||
| chr11:89185946 | A | T | 1 | a0001c0001t0001g0275 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.820-5256A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185946 | |||||||
| chr11:89185980 | G | C | 1 | a0001c0001t0001g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.820-5222G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89185980 | |||||||
| chr11:89186157 | A | G | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0118 others(12): Show |
15 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.820-5045A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186157 | |||||||
| chr11:89186184 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-5018T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186184 | |||||||
| chr11:89186194 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.820-5008T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186194 | |||||||
| chr11:89186252 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-4950G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186252 | |||||||
| chr11:89186460 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.820-4742T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186460 | |||||||
| chr11:89186648 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0015 others(53): Show |
59 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.820-4554C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186648 | |||||||
| chr11:89186660 | C | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-4542C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186660 | |||||||
| chr11:89186671 | G | A | 3 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 |
3 | HG02886.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.820-4531G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186671 | |||||||
| chr11:89186688 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.820-4514A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186688 | |||||||
| chr11:89186702 | G | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(83): Show |
88 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.820-4500G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186702 | |||||||
| chr11:89186737 | T | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(157): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.820-4465T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186737 | |||||||
| chr11:89186784 | T | G | 87 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(84): Show |
89 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(86): Show |
intron_variant | MODIFIER | c.820-4418T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186784 | |||||||
| chr11:89186801 | G | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.820-4401G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186801 | |||||||
| chr11:89186804 | G | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(67): Show |
72 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.820-4398G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186804 | |||||||
| chr11:89186848 | G | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(67): Show |
72 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.820-4354G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186848 | |||||||
| chr11:89186901 | C | T | 1 | a0001c0001t0001g0005 | 2 | NA18961.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.820-4301C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186901 | |||||||
| chr11:89186909 | A | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.820-4293A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186909 | |||||||
| chr11:89186911 | C | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(34): Show |
38 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.820-4291C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186911 | |||||||
| chr11:89186943 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.820-4259T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89186943 | |||||||
| chr11:89187292 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.820-3910C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89187292 | |||||||
| chr11:89187453 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820-3749G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89187453 | |||||||
| chr11:89187507 | C | T | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.820-3695C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89187507 | |||||||
| chr11:89187639 | C | G | 1 | a0001c0001t0001g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.820-3563C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89187639 | |||||||
| chr11:89187644 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820-3558C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89187644 | |||||||
| chr11:89187797 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.820-3405T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89187797 | |||||||
| chr11:89187891 | T | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(35): Show |
39 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.820-3311T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89187891 | |||||||
| chr11:89188069 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3133A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188069 | |||||||
| chr11:89188070 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3132G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188070 | |||||||
| chr11:89188073 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3129A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188073 | |||||||
| chr11:89188074 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3128A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188074 | |||||||
| chr11:89188081 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3121T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188081 | |||||||
| chr11:89188097 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3105T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188097 | |||||||
| chr11:89188109 | C | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(34): Show |
38 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.820-3093C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188109 | |||||||
| chr11:89188190 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3012A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188190 | |||||||
| chr11:89188195 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3007A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188195 | |||||||
| chr11:89188199 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-3003G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188199 | |||||||
| chr11:89188231 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-2971G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188231 | |||||||
| chr11:89188231 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-2971G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188231 | |||||||
| chr11:89188237 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-2965A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188237 | |||||||
| chr11:89188247 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-2955G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188247 | |||||||
| chr11:89188255 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.820-2947T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188255 | |||||||
| chr11:89188256 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.820-2946T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188256 | |||||||
| chr11:89188257 | A | G | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-2945A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188257 | |||||||
| chr11:89188269 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.820-2933A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188269 | |||||||
| chr11:89188270 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.820-2932C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188270 | |||||||
| chr11:89188347 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.820-2855A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188347 | |||||||
| chr11:89188356 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0015 others(53): Show |
59 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.820-2846C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188356 | |||||||
| chr11:89188389 | C | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(197): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.820-2813C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188389 | |||||||
| chr11:89188404 | C | A | 10 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0017 others(7): Show |
12 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.820-2798C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188404 | |||||||
| chr11:89188507 | G | A | 13 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(10): Show |
13 | HG01074.hp2 HG01099.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.820-2695G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188507 | |||||||
| chr11:89188679 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820-2523G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188679 | |||||||
| chr11:89188707 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.820-2495G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188707 | |||||||
| chr11:89188728 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0073 others(36): Show |
40 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.820-2474G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188728 | |||||||
| chr11:89188748 | C | A | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-2454C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188748 | |||||||
| chr11:89188840 | G | T | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.820-2362G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188840 | |||||||
| chr11:89188900 | G | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.820-2302G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188900 | |||||||
| chr11:89188913 | A | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(67): Show |
72 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.820-2289A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89188913 | |||||||
| chr11:89189030 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.820-2172C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189030 | |||||||
| chr11:89189295 | G | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(67): Show |
72 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.820-1907G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189295 | |||||||
| chr11:89189336 | T | A | 17 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0118 others(14): Show |
17 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.820-1866T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189336 | |||||||
| chr11:89189350 | C | T | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-1852C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189350 | |||||||
| chr11:89189353 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.820-1849T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189353 | |||||||
| chr11:89189387 | A | G | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.820-1815A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189387 | |||||||
| chr11:89189405 | C | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | NA18949.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.820-1797C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189405 | |||||||
| chr11:89189448 | CA | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.820-1744delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 89189448 | ||||||
| chr11:89189455 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820-1747A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189455 | |||||||
| chr11:89189541 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.820-1661T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189541 | |||||||
| chr11:89189720 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.820-1482G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189720 | |||||||
| chr11:89189764 | TA | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.820-1435delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 89189764 | ||||||
| chr11:89189885 | G | A | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-1317G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189885 | |||||||
| chr11:89189963 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0213 a0001c0001t0001g0214 others(15): Show |
19 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.820-1239C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89189963 | |||||||
| chr11:89190013 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.820-1189T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190013 | |||||||
| chr11:89190073 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820-1129G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190073 | |||||||
| chr11:89190119 | T | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.820-1083T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190119 | |||||||
| chr11:89190247 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820-955C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190247 | |||||||
| chr11:89190255 | T | C | 1 | a0002c0002t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.820-947T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190255 | |||||||
| chr11:89190293 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.820-909T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190293 | |||||||
| chr11:89190361 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.820-841C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190361 | |||||||
| chr11:89190361 | C | CT | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG01884.hp1 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.820-838dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 89190361 | ||||||
| chr11:89190450 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.820-752T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190450 | |||||||
| chr11:89190510 | T | A | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.820-692T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190510 | |||||||
| chr11:89190510 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820-692T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190510 | |||||||
| chr11:89190690 | G | C | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-512G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190690 | |||||||
| chr11:89190725 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.820-477T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190725 | |||||||
| chr11:89190732 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.820-470T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190732 | |||||||
| chr11:89190805 | T | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(67): Show |
72 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.820-397T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89190805 | |||||||
| chr11:89191078 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0119 others(3): Show |
6 | HG02615.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-124C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89191078 | |||||||
| chr11:89191172 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.820-30A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 1/4 | chr11 | 89191172 | |||||||
| chr11:89191651 | T | G | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02572.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1036+233T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89191651 | |||||||
| chr11:89191773 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+355G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89191773 | |||||||
| chr11:89191786 | A | C | 9 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0277 others(6): Show |
9 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1036+368A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89191786 | |||||||
| chr11:89191908 | C | T | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG02165.hp1 NA18944.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+490C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89191908 | |||||||
| chr11:89191927 | A | G | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | NA18992.hp1 NA19002.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036+509A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89191927 | |||||||
| chr11:89191971 | C | G | 1 | a0001c0001t0001g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1036+553C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89191971 | |||||||
| chr11:89191974 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1036+556C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89191974 | |||||||
| chr11:89192074 | G | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(54): Show |
60 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1036+656G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192074 | |||||||
| chr11:89192152 | A | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0193 a0001c0001t0001g0194 others(7): Show |
10 | HG01981.hp2 NA18612.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+734A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192152 | |||||||
| chr11:89192160 | A | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1036+742A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192160 | |||||||
| chr11:89192249 | A | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+831A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192249 | |||||||
| chr11:89192316 | C | CA | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+907dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89192316 | ||||||
| chr11:89192632 | T | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+1214T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192632 | |||||||
| chr11:89192787 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(158): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1036+1369T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192787 | |||||||
| chr11:89192895 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1036+1477T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192895 | |||||||
| chr11:89192973 | T | C | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0118 others(4): Show |
7 | HG01243.hp2 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+1555T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89192973 | |||||||
| chr11:89193006 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1036+1588C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193006 | |||||||
| chr11:89193012 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1036+1594C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193012 | |||||||
| chr11:89193223 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1036+1805G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193223 | |||||||
| chr11:89193275 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+1857T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193275 | |||||||
| chr11:89193312 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1036+1894C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193312 | |||||||
| chr11:89193313 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(83): Show |
88 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.1036+1895G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193313 | |||||||
| chr11:89193375 | TC | T | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+1958delC | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193375 | |||||||
| chr11:89193408 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1036+1990G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193408 | |||||||
| chr11:89193439 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1036+2021A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193439 | |||||||
| chr11:89193569 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+2151G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193569 | |||||||
| chr11:89193652 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+2234C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193652 | |||||||
| chr11:89193801 | G | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+2383G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193801 | |||||||
| chr11:89193870 | TTC | T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(159): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1036+2467_1036+246 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89193870 | ||||||
| chr11:89193993 | A | C | 18 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(15): Show |
18 | HG01074.hp2 HG01099.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1036+2575A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89193993 | |||||||
| chr11:89194056 | C | A | 1 | a0001c0001t0002g0208 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1036+2638C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194056 | |||||||
| chr11:89194092 | T | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0213 a0001c0001t0001g0214 others(15): Show |
19 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1036+2674T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194092 | |||||||
| chr11:89194174 | A | C | 1 | a0002c0002t0001g0192 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1036+2756A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194174 | |||||||
| chr11:89194240 | C | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(83): Show |
88 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.1036+2822C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194240 | |||||||
| chr11:89194241 | AT | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02572.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1036+2830delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89194241 | ||||||
| chr11:89194283 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1036+2865T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194283 | |||||||
| chr11:89194331 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+2913A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194331 | |||||||
| chr11:89194389 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1036+2971C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194389 | |||||||
| chr11:89194447 | T | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18940.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1036+3029T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194447 | |||||||
| chr11:89194485 | A | G | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+3067A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194485 | |||||||
| chr11:89194498 | AAGAC | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 others(36): Show |
40 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.1036+3081_1036+308 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194498 | |||||||
| chr11:89194531 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1036+3113T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194531 | |||||||
| chr11:89194550 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1036+3132C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194550 | |||||||
| chr11:89194565 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+3147A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194565 | |||||||
| chr11:89194650 | T | TTCTA | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0026 others(40): Show |
45 | HG00639.hp2 HG00741.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1036+3263_1036+326 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89194650 | ||||||
| chr11:89194650 | T | TTCTATCT others(1): Show |
55 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0071 others(52): Show |
57 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1036+3259_1036+326 others(12): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89194650 | ||||||
| chr11:89194650 | T | TTCTATCT others(5): Show |
27 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0074 others(24): Show |
27 | HG01099.hp1 HG01358.hp2 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.1036+3255_1036+326 others(16): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89194650 | ||||||
| chr11:89194650 | T | TTCTATCT others(9): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0219 |
3 | HG03130.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1036+3251_1036+326 others(20): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89194650 | ||||||
| chr11:89194650 | TTCTA | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(56): Show |
61 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1036+3263_1036+326 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89194650 | ||||||
| chr11:89194650 | TTCTATCT others(1): Show |
T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+3259_1036+326 others(12): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89194650 | ||||||
| chr11:89194932 | A | G | 1 | a0001c0001t0001g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1036+3514A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194932 | |||||||
| chr11:89194964 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(89): Show |
intron_variant | MODIFIER | c.1036+3546C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194964 | |||||||
| chr11:89194979 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0295 |
2 | HG01346.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1036+3561C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194979 | |||||||
| chr11:89194980 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
7 | HG00639.hp1 HG00642.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+3562G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89194980 | |||||||
| chr11:89195021 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1036+3603C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195021 | |||||||
| chr11:89195035 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+3617C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195035 | |||||||
| chr11:89195075 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1036+3657T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195075 | |||||||
| chr11:89195186 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+3768C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195186 | |||||||
| chr11:89195222 | A | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1036+3804A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195222 | |||||||
| chr11:89195238 | C | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 others(36): Show |
40 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.1036+3820C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195238 | |||||||
| chr11:89195343 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1036+3925A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195343 | |||||||
| chr11:89195416 | C | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+3998C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195416 | |||||||
| chr11:89195508 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036+4090G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195508 | |||||||
| chr11:89195598 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+4180G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195598 | |||||||
| chr11:89195667 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(89): Show |
intron_variant | MODIFIER | c.1036+4249C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195667 | |||||||
| chr11:89195669 | C | CATAA | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4273_1036+427 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89195669 | ||||||
| chr11:89195669 | CATAA | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.1036+4273_1036+427 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89195669 | ||||||
| chr11:89195737 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0235 a0001c0001t0001g0236 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1036+4319A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195737 | |||||||
| chr11:89195746 | T | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG01081.hp1 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1036+4328T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195746 | |||||||
| chr11:89195750 | A | T | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+4332A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195750 | |||||||
| chr11:89195799 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1036+4381T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195799 | |||||||
| chr11:89195894 | TTTTA | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG00099.hp2 HG01978.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+4484_1036+448 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89195894 | ||||||
| chr11:89195985 | A | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+4567A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89195985 | |||||||
| chr11:89196049 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1036+4631T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196049 | |||||||
| chr11:89196110 | G | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+4692G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196110 | |||||||
| chr11:89196182 | A | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+4764A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196182 | |||||||
| chr11:89196241 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1036+4823C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196241 | |||||||
| chr11:89196317 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1036+4899A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196317 | |||||||
| chr11:89196317 | A | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(68): Show |
73 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.1036+4899A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196317 | |||||||
| chr11:89196363 | A | G | 18 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(15): Show |
18 | HG01074.hp2 HG01099.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1036+4945A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196363 | |||||||
| chr11:89196456 | C | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(82): Show |
intron_variant | MODIFIER | c.1036+5038C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196456 | |||||||
| chr11:89196463 | T | C | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG00099.hp2 HG01978.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+5045T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196463 | |||||||
| chr11:89196516 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+5098G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196516 | |||||||
| chr11:89196703 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+5285A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196703 | |||||||
| chr11:89196903 | G | C | 1 | a0002c0002t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1036+5485G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196903 | |||||||
| chr11:89196938 | C | T | 91 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(88): Show |
93 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(90): Show |
intron_variant | MODIFIER | c.1036+5520C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196938 | |||||||
| chr11:89196980 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0233 a0001c0001t0001g0277 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+5562C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89196980 | |||||||
| chr11:89197018 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1036+5600A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197018 | |||||||
| chr11:89197209 | A | G | 60 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
63 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1036+5791A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197209 | |||||||
| chr11:89197228 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1036+5810G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197228 | |||||||
| chr11:89197323 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1036+5905G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197323 | |||||||
| chr11:89197413 | A | G | 44 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
46 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1036+5995A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197413 | |||||||
| chr11:89197415 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1036+5997T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197415 | |||||||
| chr11:89197416 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0213 a0001c0001t0001g0214 others(15): Show |
19 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1036+5998C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197416 | |||||||
| chr11:89197483 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1036+6065T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197483 | |||||||
| chr11:89197619 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+6201T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197619 | |||||||
| chr11:89197732 | G | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+6314G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197732 | |||||||
| chr11:89197739 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(42): Show |
47 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1036+6321G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197739 | |||||||
| chr11:89197765 | A | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0213 a0001c0001t0001g0223 others(9): Show |
13 | HG00280.hp2 HG01358.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1036+6347A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89197765 | |||||||
| chr11:89197898 | GCTTC | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(89): Show |
intron_variant | MODIFIER | c.1036+6485_1036+648 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89197898 | ||||||
| chr11:89198093 | A | T | 1 | a0001c0001t0001g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1036+6675A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198093 | |||||||
| chr11:89198118 | T | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+6700T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198118 | |||||||
| chr11:89198135 | C | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+6717C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198135 | |||||||
| chr11:89198227 | C | CA | 20 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(17): Show |
20 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1036+6818dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198227 | ||||||
| chr11:89198319 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0015 others(53): Show |
59 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1036+6901C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198319 | |||||||
| chr11:89198320 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(90): Show |
95 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(92): Show |
intron_variant | MODIFIER | c.1036+6902G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198320 | |||||||
| chr11:89198346 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1036+6928T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198346 | |||||||
| chr11:89198388 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1036+6970A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198388 | |||||||
| chr11:89198416 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1036+6998C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198416 | |||||||
| chr11:89198468 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(89): Show |
intron_variant | MODIFIER | c.1036+7050C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198468 | |||||||
| chr11:89198754 | C | CAT | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+7351_1036+735 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATAT | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(6): Show |
9 | HG00099.hp2 HG01978.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1036+7347_1036+735 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATATA others(1): Show |
37 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0072 others(34): Show |
37 | HG01516.hp1 HG01884.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1036+7345_1036+735 others(12): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATATA others(3): Show |
31 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0070 others(28): Show |
33 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.1036+7343_1036+735 others(14): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1036+7339_1036+735 others(18): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATATA others(19): Show |
3 | a0001c0004t0001g0283 a0001c0004t0001g0287 a0001c0004t0001g0288 |
3 | HG02451.hp2 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1036+7352_1036+735 others(30): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATATA others(21): Show |
1 | a0001c0004t0001g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1036+7352_1036+735 others(32): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATATA others(23): Show |
1 | a0001c0004t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1036+7352_1036+735 others(34): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198754 | C | CATATATA others(25): Show |
1 | a0001c0004t0001g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1036+7352_1036+735 others(36): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198754 | ||||||
| chr11:89198769 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG01099.hp1 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+7352_1036+735 others(21): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198769 | ||||||
| chr11:89198769 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01074.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1036+7352_1036+735 others(19): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89198769 | ||||||
| chr11:89198771 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1036+7353T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198771 | |||||||
| chr11:89198816 | T | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+7398T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198816 | |||||||
| chr11:89198882 | G | A | 11 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(8): Show |
11 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036+7464G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198882 | |||||||
| chr11:89198936 | G | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+7518G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89198936 | |||||||
| chr11:89199047 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1036+7629G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199047 | |||||||
| chr11:89199088 | A | T | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+7670A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199088 | |||||||
| chr11:89199169 | A | T | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+7751A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199169 | |||||||
| chr11:89199212 | A | G | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+7794A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199212 | |||||||
| chr11:89199220 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1036+7802T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199220 | |||||||
| chr11:89199222 | T | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.1036+7804T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199222 | |||||||
| chr11:89199449 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02622.hp2 HG02818.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1036+8031T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199449 | |||||||
| chr11:89199595 | C | T | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+8177C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199595 | |||||||
| chr11:89199872 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1036+8454T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199872 | |||||||
| chr11:89199937 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1036+8519C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89199937 | |||||||
| chr11:89200044 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1036+8626A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89200044 | |||||||
| chr11:89200082 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1036+8664C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89200082 | |||||||
| chr11:89200237 | C | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | NA18983.hp2 NA18995.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1036+8819C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89200237 | |||||||
| chr11:89200242 | A | AT | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+8831dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89200242 | ||||||
| chr11:89200243 | T | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG01081.hp1 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1036+8825T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89200243 | |||||||
| chr11:89200461 | C | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1036+9043C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89200461 | |||||||
| chr11:89200490 | T | C | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1036+9072T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89200490 | |||||||
| chr11:89200549 | ACTT | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+9134_1036+913 others(7): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89200549 | ||||||
| chr11:89200616 | TTTG | T | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+9201_1036+920 others(7): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89200616 | ||||||
| chr11:89200687 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1036+9269T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89200687 | |||||||
| chr11:89201057 | T | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02683.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1036+9639T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201057 | |||||||
| chr11:89201110 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+9692C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201110 | |||||||
| chr11:89201166 | T | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+9748T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201166 | |||||||
| chr11:89201227 | GA | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(3): Show |
6 | HG01346.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+9817delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89201227 | ||||||
| chr11:89201227 | GAA | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+9816_1036+981 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89201227 | ||||||
| chr11:89201339 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1036+9921A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201339 | |||||||
| chr11:89201518 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1036+10100A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201518 | |||||||
| chr11:89201588 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1036+10170C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201588 | |||||||
| chr11:89201742 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1036+10324T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201742 | |||||||
| chr11:89201828 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+10410G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201828 | |||||||
| chr11:89201863 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(35): Show |
39 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.1036+10445C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201863 | |||||||
| chr11:89201864 | A | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+10446A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201864 | |||||||
| chr11:89201900 | G | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1036+10482G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201900 | |||||||
| chr11:89201920 | C | T | 16 | a0002c0002t0001g0007 a0002c0002t0001g0132 a0002c0002t0001g0136 others(13): Show |
17 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1036+10502C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201920 | |||||||
| chr11:89201928 | G | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+10510G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89201928 | |||||||
| chr11:89202020 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG00323.hp1 HG01081.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+10602G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202020 | |||||||
| chr11:89202190 | C | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+10772C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202190 | |||||||
| chr11:89202192 | T | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1036+10774T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202192 | |||||||
| chr11:89202237 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1036+10819A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202237 | |||||||
| chr11:89202268 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1036+10850G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202268 | |||||||
| chr11:89202315 | A | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+10897A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202315 | |||||||
| chr11:89202417 | G | GT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(8): Show |
11 | HG02615.hp1 HG02896.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1036+11009dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202417 | ||||||
| chr11:89202551 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+11133G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202551 | |||||||
| chr11:89202622 | T | TAC | 16 | a0002c0002t0001g0007 a0002c0002t0001g0132 a0002c0002t0001g0136 others(13): Show |
17 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1036+11231_1036+11 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1036+11223_1036+11 others(16): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(5): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0276 |
2 | HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1036+11221_1036+11 others(18): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(9): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01943.hp2 HG01975.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+11217_1036+11 others(22): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(11): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+11217_1036+11 others(24): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(13): Show |
51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
53 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1036+11217_1036+11 others(26): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(7): Show |
11 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0158 others(8): Show |
11 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1036+11219_1036+11 others(20): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(9): Show |
24 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(21): Show |
24 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1036+11217_1036+11 others(22): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(13): Show |
37 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0097 others(34): Show |
37 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1036+11213_1036+11 others(26): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(15): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0096 others(32): Show |
37 | HG00639.hp1 HG01255.hp2 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.1036+11211_1036+11 others(28): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(17): Show |
28 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0084 others(25): Show |
29 | HG00140.hp2 HG00642.hp1 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.1036+11209_1036+11 others(30): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACACACA others(19): Show |
6 | a0001c0001t0001g0092 a0001c0001t0001g0103 a0001c0001t0001g0115 others(3): Show |
6 | HG03491.hp2 NA18940.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+11207_1036+11 others(32): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202622 | T | TACATACA others(13): Show |
1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+11207_1036+11 others(26): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89202622 | ||||||
| chr11:89202652 | G | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(86): Show |
91 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(88): Show |
intron_variant | MODIFIER | c.1036+11234G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202652 | |||||||
| chr11:89202677 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1036+11259A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202677 | |||||||
| chr11:89202692 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+11274C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202692 | |||||||
| chr11:89202732 | C | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01243.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+11314C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202732 | |||||||
| chr11:89202773 | T | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(160): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1036+11355T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202773 | |||||||
| chr11:89202839 | T | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(160): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1036+11421T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202839 | |||||||
| chr11:89202965 | G | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.1036+11547G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202965 | |||||||
| chr11:89202979 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1036+11561A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89202979 | |||||||
| chr11:89203129 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+11711C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203129 | |||||||
| chr11:89203177 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1036+11759T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203177 | |||||||
| chr11:89203344 | G | A | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(162): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1036+11926G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203344 | |||||||
| chr11:89203405 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG02970.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1036+11987C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203405 | |||||||
| chr11:89203498 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG00558.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1036+12080C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203498 | |||||||
| chr11:89203543 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1036+12125T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203543 | |||||||
| chr11:89203641 | T | C | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+12223T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203641 | |||||||
| chr11:89203654 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1036+12236C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203654 | |||||||
| chr11:89203655 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02572.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1036+12237G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203655 | |||||||
| chr11:89203760 | A | G | 9 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 others(6): Show |
9 | HG01346.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1036+12342A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89203760 | |||||||
| chr11:89204048 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1036+12630A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204048 | |||||||
| chr11:89204131 | T | C | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+12713T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204131 | |||||||
| chr11:89204244 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1036+12826G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204244 | |||||||
| chr11:89204348 | G | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+12930G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204348 | |||||||
| chr11:89204397 | A | AT | 13 | a0001c0001t0001g0012 a0001c0001t0001g0068 a0001c0001t0001g0069 others(10): Show |
13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1036+12992dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89204397 | ||||||
| chr11:89204397 | AT | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(71): Show |
76 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(73): Show |
intron_variant | MODIFIER | c.1036+12992delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89204397 | ||||||
| chr11:89204398 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG01884.hp1 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1036+12980T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204398 | |||||||
| chr11:89204434 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1036+13016T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204434 | |||||||
| chr11:89204447 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1036+13029A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204447 | |||||||
| chr11:89204468 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+13050A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204468 | |||||||
| chr11:89204542 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+13124C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204542 | |||||||
| chr11:89204555 | C | T | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+13137C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204555 | |||||||
| chr11:89204561 | AT | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+13151delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89204561 | ||||||
| chr11:89204569 | T | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0213 others(16): Show |
20 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1036+13151T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204569 | |||||||
| chr11:89204573 | T | G | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+13155T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204573 | |||||||
| chr11:89204588 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1036+13170G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204588 | |||||||
| chr11:89204765 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1036+13347T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204765 | |||||||
| chr11:89204824 | T | TAA | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+13419_1036+13 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89204824 | ||||||
| chr11:89204824 | TA | T | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0095 others(7): Show |
10 | HG01167.hp2 HG02615.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1036+13420delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89204824 | ||||||
| chr11:89204850 | T | G | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.1036+13432T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89204850 | |||||||
| chr11:89205053 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1036+13635C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205053 | |||||||
| chr11:89205054 | G | A | 7 | a0001c0001t0001g0073 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+13636G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205054 | |||||||
| chr11:89205123 | A | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0213 others(16): Show |
20 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1036+13705A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205123 | |||||||
| chr11:89205188 | A | G | 60 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
63 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1036+13770A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205188 | |||||||
| chr11:89205193 | A | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01243.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+13775A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205193 | |||||||
| chr11:89205197 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+13779T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205197 | |||||||
| chr11:89205245 | A | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+13827A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205245 | |||||||
| chr11:89205249 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1036+13831A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205249 | |||||||
| chr11:89205299 | T | C | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+13881T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205299 | |||||||
| chr11:89205303 | T | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(78): Show |
intron_variant | MODIFIER | c.1036+13885T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205303 | |||||||
| chr11:89205403 | A | T | 91 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(88): Show |
93 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(90): Show |
intron_variant | MODIFIER | c.1036+13985A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205403 | |||||||
| chr11:89205567 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+14149G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205567 | |||||||
| chr11:89205573 | A | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+14155A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205573 | |||||||
| chr11:89205598 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1036+14180T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205598 | |||||||
| chr11:89205765 | G | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(54): Show |
60 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1036+14347G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205765 | |||||||
| chr11:89205811 | C | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(79): Show |
84 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.1036+14393C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205811 | |||||||
| chr11:89205840 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(160): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1036+14422A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205840 | |||||||
| chr11:89205879 | A | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+14461A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205879 | |||||||
| chr11:89205989 | C | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+14571C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89205989 | |||||||
| chr11:89206322 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1036+14904T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206322 | |||||||
| chr11:89206397 | A | T | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1036+14979A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206397 | |||||||
| chr11:89206554 | A | G | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+15136A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206554 | |||||||
| chr11:89206661 | T | TAAC | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(160): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1036+15252_1036+15 others(9): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89206661 | ||||||
| chr11:89206676 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1036+15258A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206676 | |||||||
| chr11:89206810 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG01884.hp1 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1036+15392G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206810 | |||||||
| chr11:89206885 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1036+15467A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206885 | |||||||
| chr11:89206983 | G | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036+15565G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206983 | |||||||
| chr11:89206999 | A | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036+15581A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89206999 | |||||||
| chr11:89207058 | C | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(67): Show |
72 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.1036+15640C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207058 | |||||||
| chr11:89207147 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1036+15729A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207147 | |||||||
| chr11:89207166 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+15748G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207166 | |||||||
| chr11:89207283 | G | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01243.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+15865G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207283 | |||||||
| chr11:89207292 | A | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(90): Show |
95 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(92): Show |
intron_variant | MODIFIER | c.1036+15874A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207292 | |||||||
| chr11:89207329 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1036+15911G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207329 | |||||||
| chr11:89207458 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG02970.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1036+16040G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207458 | |||||||
| chr11:89207588 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1036+16170G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207588 | |||||||
| chr11:89207671 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1036+16253C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207671 | |||||||
| chr11:89207716 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1036+16298C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207716 | |||||||
| chr11:89207717 | GAATAT | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+16303_1036+16 others(11): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89207717 | ||||||
| chr11:89207735 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1036+16317T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207735 | |||||||
| chr11:89207996 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00609.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1036+16578C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207996 | |||||||
| chr11:89207997 | G | C | 7 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036+16579G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207997 | |||||||
| chr11:89207997 | G | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+16579G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89207997 | |||||||
| chr11:89208006 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0067 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+16588C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208006 | |||||||
| chr11:89208037 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1036+16619G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208037 | |||||||
| chr11:89208040 | G | A | 37 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(34): Show |
38 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.1036+16622G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208040 | |||||||
| chr11:89208054 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+16636G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208054 | |||||||
| chr11:89208096 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.1036+16678G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208096 | |||||||
| chr11:89208112 | C | CA | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+16702dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89208112 | ||||||
| chr11:89208209 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+16791G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208209 | |||||||
| chr11:89208259 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1036+16841G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208259 | |||||||
| chr11:89208302 | G | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+16884G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208302 | |||||||
| chr11:89208359 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+16941G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208359 | |||||||
| chr11:89208371 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1036+16953C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208371 | |||||||
| chr11:89208460 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1036+17042T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208460 | |||||||
| chr11:89208618 | A | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+17200A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208618 | |||||||
| chr11:89208631 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1036+17213G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208631 | |||||||
| chr11:89208668 | G | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1036+17250G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208668 | |||||||
| chr11:89208742 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0228 |
3 | HG00280.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1036+17324A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208742 | |||||||
| chr11:89208782 | G | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1036+17364G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208782 | |||||||
| chr11:89208813 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1036+17395A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208813 | |||||||
| chr11:89208850 | G | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.1036+17432G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89208850 | |||||||
| chr11:89209145 | T | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(160): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1036+17727T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209145 | |||||||
| chr11:89209472 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1036+18054G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209472 | |||||||
| chr11:89209624 | G | A | 1 | a0003c0003t0001g0017 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1037-18199G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209624 | |||||||
| chr11:89209634 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-18189C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209634 | |||||||
| chr11:89209635 | G | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1037-18188G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209635 | |||||||
| chr11:89209771 | G | A | 1 | a0003c0003t0001g0018 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1037-18052G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209771 | |||||||
| chr11:89209788 | G | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-18035G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209788 | |||||||
| chr11:89209852 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1037-17971C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209852 | |||||||
| chr11:89209867 | T | C | 9 | a0003c0003t0001g0002 a0003c0003t0001g0003 a0003c0003t0001g0017 others(6): Show |
11 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1037-17956T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209867 | |||||||
| chr11:89209871 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-17952G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209871 | |||||||
| chr11:89209956 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1037-17867T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209956 | |||||||
| chr11:89209985 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-17838G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89209985 | |||||||
| chr11:89210014 | A | G | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-17809A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210014 | |||||||
| chr11:89210124 | A | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-17699A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210124 | |||||||
| chr11:89210149 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1037-17674G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210149 | |||||||
| chr11:89210182 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | NA18946.hp1 NA18947.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1037-17641G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210182 | |||||||
| chr11:89210253 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1037-17570A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210253 | |||||||
| chr11:89210316 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-17507G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210316 | |||||||
| chr11:89210339 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-17484C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210339 | |||||||
| chr11:89210346 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037-17477A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210346 | |||||||
| chr11:89210362 | G | GGATATCA others(2): Show |
162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(159): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1037-17458_1037-17 others(15): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89210362 | ||||||
| chr11:89210366 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.1037-17457T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210366 | |||||||
| chr11:89210381 | TGAAATAA others(5): Show |
T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(159): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1037-17426_1037-17 others(18): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89210381 | ||||||
| chr11:89210462 | G | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0026 others(38): Show |
43 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.1037-17361G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210462 | |||||||
| chr11:89210504 | G | A | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1037-17319G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210504 | |||||||
| chr11:89210515 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1037-17308C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210515 | |||||||
| chr11:89210585 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1037-17238G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210585 | |||||||
| chr11:89210586 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-17237G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210586 | |||||||
| chr11:89210650 | C | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1037-17173C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210650 | |||||||
| chr11:89210988 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-16835G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89210988 | |||||||
| chr11:89211023 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037-16800G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211023 | |||||||
| chr11:89211031 | A | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-16792A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211031 | |||||||
| chr11:89211199 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(90): Show |
95 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(92): Show |
intron_variant | MODIFIER | c.1037-16624A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211199 | |||||||
| chr11:89211330 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-16493T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211330 | |||||||
| chr11:89211338 | A | T | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037-16485A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211338 | |||||||
| chr11:89211494 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-16329A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211494 | |||||||
| chr11:89211570 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | NA18992.hp1 NA19002.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-16253G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211570 | |||||||
| chr11:89211577 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1037-16246G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211577 | |||||||
| chr11:89211583 | G | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.1037-16240G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211583 | |||||||
| chr11:89211698 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1037-16125G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211698 | |||||||
| chr11:89211759 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-16064A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211759 | |||||||
| chr11:89211793 | T | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1037-16030T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211793 | |||||||
| chr11:89211950 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.1037-15873G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89211950 | |||||||
| chr11:89212017 | C | A | 11 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(8): Show |
11 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1037-15806C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212017 | |||||||
| chr11:89212118 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1037-15705C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212118 | |||||||
| chr11:89212152 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-15671C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212152 | |||||||
| chr11:89212169 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-15654A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212169 | |||||||
| chr11:89212188 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1037-15635G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212188 | |||||||
| chr11:89212243 | G | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-15580G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212243 | |||||||
| chr11:89212355 | TCAA | T | 6 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-15465_1037-15 others(9): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89212355 | ||||||
| chr11:89212418 | C | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.1037-15405C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212418 | |||||||
| chr11:89212491 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1037-15332C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212491 | |||||||
| chr11:89212569 | CCTT | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
74 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(71): Show |
intron_variant | MODIFIER | c.1037-15250_1037-15 others(9): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89212569 | ||||||
| chr11:89212590 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-15233G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212590 | |||||||
| chr11:89212752 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.1037-15071G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212752 | |||||||
| chr11:89212762 | C | T | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1037-15061C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212762 | |||||||
| chr11:89212888 | A | C | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-14935A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212888 | |||||||
| chr11:89212910 | C | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0213 others(16): Show |
20 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1037-14913C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212910 | |||||||
| chr11:89212971 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-14852G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212971 | |||||||
| chr11:89212982 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-14841T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89212982 | |||||||
| chr11:89213068 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-14755A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89213068 | |||||||
| chr11:89213431 | T | C | 7 | a0001c0001t0001g0118 a0001c0004t0001g0283 a0001c0004t0001g0284 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-14392T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89213431 | |||||||
| chr11:89213574 | T | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(82): Show |
87 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(84): Show |
intron_variant | MODIFIER | c.1037-14249T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89213574 | |||||||
| chr11:89213743 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-14080T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89213743 | |||||||
| chr11:89213787 | A | G | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-14036A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89213787 | |||||||
| chr11:89213898 | T | A | 80 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1037-13925T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89213898 | |||||||
| chr11:89213964 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1037-13859T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89213964 | |||||||
| chr11:89214113 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-13710T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214113 | |||||||
| chr11:89214409 | T | C | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-13414T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214409 | |||||||
| chr11:89214467 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-13356A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214467 | |||||||
| chr11:89214486 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-13337G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214486 | |||||||
| chr11:89214578 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-13245C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214578 | |||||||
| chr11:89214595 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0213 others(16): Show |
20 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1037-13228G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214595 | |||||||
| chr11:89214697 | G | C | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-13126G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214697 | |||||||
| chr11:89214756 | G | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1037-13067G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214756 | |||||||
| chr11:89214838 | A | T | 92 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(89): Show |
94 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1037-12985A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89214838 | |||||||
| chr11:89215109 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1037-12714G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215109 | |||||||
| chr11:89215151 | A | T | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1037-12672A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215151 | |||||||
| chr11:89215171 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0076 others(17): Show |
21 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1037-12652T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215171 | |||||||
| chr11:89215184 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1037-12639G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215184 | |||||||
| chr11:89215205 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-12618C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215205 | |||||||
| chr11:89215379 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1037-12444G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215379 | |||||||
| chr11:89215428 | G | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-12395G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215428 | |||||||
| chr11:89215453 | G | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
76 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(73): Show |
intron_variant | MODIFIER | c.1037-12370G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215453 | |||||||
| chr11:89215516 | T | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-12307T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215516 | |||||||
| chr11:89215525 | T | TAATAA | 95 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(92): Show |
97 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(94): Show |
intron_variant | MODIFIER | c.1037-12285_1037-12 others(11): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89215525 | ||||||
| chr11:89215567 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-12256T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215567 | |||||||
| chr11:89215637 | A | AT | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-12180dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89215637 | ||||||
| chr11:89215772 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18971.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1037-12051T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215772 | |||||||
| chr11:89215829 | A | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-11994A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215829 | |||||||
| chr11:89215896 | T | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-11927T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215896 | |||||||
| chr11:89215936 | C | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(82): Show |
87 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(84): Show |
intron_variant | MODIFIER | c.1037-11887C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89215936 | |||||||
| chr11:89216112 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-11711T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216112 | |||||||
| chr11:89216131 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-11692T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216131 | |||||||
| chr11:89216154 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-11669C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216154 | |||||||
| chr11:89216328 | C | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-11495C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216328 | |||||||
| chr11:89216381 | A | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(89): Show |
94 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1037-11442A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216381 | |||||||
| chr11:89216433 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1037-11390C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216433 | |||||||
| chr11:89216550 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-11273G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216550 | |||||||
| chr11:89216561 | G | C | 74 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
76 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(73): Show |
intron_variant | MODIFIER | c.1037-11262G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216561 | |||||||
| chr11:89216647 | C | CA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(100): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1037-11154dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAA | 14 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0036 others(11): Show |
14 | HG00558.hp1 HG01243.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1037-11155_1037-11 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAAA | 10 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0293 others(7): Show |
10 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-11156_1037-11 others(9): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAAAAA | 14 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0214 others(11): Show |
15 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1037-11158_1037-11 others(11): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAAAAAA | 10 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0225 others(7): Show |
10 | HG01074.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037-11159_1037-11 others(12): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0079 others(2): Show |
5 | HG02818.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-11164_1037-11 others(17): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0080 |
3 | HG02109.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1037-11165_1037-11 others(18): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1037-11168_1037-11 others(21): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1037-11172_1037-11 others(25): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | CAAA | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 others(35): Show |
39 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.1037-11156_1037-11 others(9): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216647 | CAAAA | C | 7 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0097 others(4): Show |
7 | HG02622.hp2 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-11157_1037-11 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216647 | ||||||
| chr11:89216702 | AAAG | A | 80 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1037-11117_1037-11 others(9): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89216702 | ||||||
| chr11:89216744 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1037-11079T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216744 | |||||||
| chr11:89216767 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1037-11056T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216767 | |||||||
| chr11:89216790 | T | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG00558.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1037-11033T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216790 | |||||||
| chr11:89216958 | T | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-10865T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89216958 | |||||||
| chr11:89217275 | T | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-10548T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217275 | |||||||
| chr11:89217307 | G | A | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-10516G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217307 | |||||||
| chr11:89217503 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1037-10320T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217503 | |||||||
| chr11:89217665 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1037-10158G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217665 | |||||||
| chr11:89217714 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-10109T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217714 | |||||||
| chr11:89217819 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0154 others(1): Show |
4 | NA18973.hp2 NA18995.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-10004G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217819 | |||||||
| chr11:89217825 | GTTTCCCA others(3): Show |
G | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1037-9996_1037-998 others(14): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89217825 | ||||||
| chr11:89217917 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1037-9906T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217917 | |||||||
| chr11:89217947 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1037-9876T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89217947 | |||||||
| chr11:89218079 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-9744C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218079 | |||||||
| chr11:89218164 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
76 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(73): Show |
intron_variant | MODIFIER | c.1037-9659C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218164 | |||||||
| chr11:89218263 | T | G | 7 | a0001c0001t0001g0118 a0001c0004t0001g0283 a0001c0004t0001g0284 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-9560T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218263 | |||||||
| chr11:89218441 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1037-9382C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218441 | |||||||
| chr11:89218469 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1037-9354G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218469 | |||||||
| chr11:89218503 | T | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0076 others(17): Show |
21 | HG00280.hp2 HG01243.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1037-9320T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218503 | |||||||
| chr11:89218710 | T | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(82): Show |
87 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(84): Show |
intron_variant | MODIFIER | c.1037-9113T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218710 | |||||||
| chr11:89218749 | T | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-9074T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218749 | |||||||
| chr11:89218864 | A | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
76 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(73): Show |
intron_variant | MODIFIER | c.1037-8959A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218864 | |||||||
| chr11:89218958 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1037-8865T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89218958 | |||||||
| chr11:89219033 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1037-8790C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219033 | |||||||
| chr11:89219085 | C | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(82): Show |
87 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(84): Show |
intron_variant | MODIFIER | c.1037-8738C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219085 | |||||||
| chr11:89219132 | A | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-8691A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219132 | |||||||
| chr11:89219179 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0235 a0001c0001t0001g0236 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1037-8644T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219179 | |||||||
| chr11:89219189 | T | C | 7 | a0001c0001t0001g0118 a0001c0004t0001g0283 a0001c0004t0001g0284 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-8634T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219189 | |||||||
| chr11:89219245 | C | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-8578C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219245 | |||||||
| chr11:89219251 | T | C | 74 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
76 | HG00099.hp2 HG00280.hp2 HG01243.hp1 others(73): Show |
intron_variant | MODIFIER | c.1037-8572T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219251 | |||||||
| chr11:89219288 | C | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1037-8535C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219288 | |||||||
| chr11:89219296 | C | CT | 15 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0068 others(12): Show |
15 | HG01081.hp1 HG02155.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1037-8510dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89219296 | ||||||
| chr11:89219296 | CT | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.1037-8510delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89219296 | ||||||
| chr11:89219356 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1037-8467G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219356 | |||||||
| chr11:89219421 | C | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-8402C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219421 | |||||||
| chr11:89219693 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-8130A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219693 | |||||||
| chr11:89219697 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-8126G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219697 | |||||||
| chr11:89219711 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-8112G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219711 | |||||||
| chr11:89219748 | C | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1037-8075C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219748 | |||||||
| chr11:89219845 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1037-7978C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219845 | |||||||
| chr11:89219862 | G | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-7961G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219862 | |||||||
| chr11:89219993 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1037-7830G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89219993 | |||||||
| chr11:89220078 | C | T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG00597.hp2 HG00609.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-7745C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220078 | |||||||
| chr11:89220088 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-7735T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220088 | |||||||
| chr11:89220137 | A | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(92): Show |
97 | HG00099.hp2 HG00280.hp2 HG01074.hp2 others(94): Show |
intron_variant | MODIFIER | c.1037-7686A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220137 | |||||||
| chr11:89220144 | T | TA | 52 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0070 others(49): Show |
53 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(50): Show |
intron_variant | MODIFIER | c.1037-7669dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89220144 | ||||||
| chr11:89220267 | A | G | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-7556A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220267 | |||||||
| chr11:89220268 | C | A | 1 | a0001c0006t0001g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1037-7555C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220268 | |||||||
| chr11:89220336 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1037-7487C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220336 | |||||||
| chr11:89220383 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1037-7440T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220383 | |||||||
| chr11:89220450 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1037-7373G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220450 | |||||||
| chr11:89220516 | G | A | 11 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(8): Show |
11 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1037-7307G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220516 | |||||||
| chr11:89220603 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1037-7220C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220603 | |||||||
| chr11:89220617 | C | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-7206C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220617 | |||||||
| chr11:89220651 | C | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1037-7172C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220651 | |||||||
| chr11:89220678 | T | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(40): Show |
45 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1037-7145T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220678 | |||||||
| chr11:89220822 | T | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(80): Show |
84 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1037-7001T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220822 | |||||||
| chr11:89220871 | A | C | 1 | a0001c0006t0001g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1037-6952A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220871 | |||||||
| chr11:89220992 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1037-6831C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89220992 | |||||||
| chr11:89221029 | A | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(82): Show |
86 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.1037-6794A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221029 | |||||||
| chr11:89221161 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-6662T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221161 | |||||||
| chr11:89221171 | C | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(90): Show |
94 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1037-6652C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221171 | |||||||
| chr11:89221336 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1037-6487T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221336 | |||||||
| chr11:89221338 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1037-6485C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221338 | |||||||
| chr11:89221460 | A | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-6363A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221460 | |||||||
| chr11:89221497 | A | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-6326A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221497 | |||||||
| chr11:89221580 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1037-6243T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221580 | |||||||
| chr11:89221623 | C | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-6200C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221623 | |||||||
| chr11:89221796 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1037-6027A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221796 | |||||||
| chr11:89221837 | G | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(75): Show |
79 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(76): Show |
intron_variant | MODIFIER | c.1037-5986G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221837 | |||||||
| chr11:89221947 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-5876C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221947 | |||||||
| chr11:89221979 | T | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(90): Show |
94 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1037-5844T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89221979 | |||||||
| chr11:89222066 | C | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(75): Show |
79 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(76): Show |
intron_variant | MODIFIER | c.1037-5757C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222066 | |||||||
| chr11:89222456 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1037-5367G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222456 | |||||||
| chr11:89222466 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1037-5357C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222466 | |||||||
| chr11:89222476 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-5347C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222476 | |||||||
| chr11:89222508 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(75): Show |
79 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(76): Show |
intron_variant | MODIFIER | c.1037-5315G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222508 | |||||||
| chr11:89222693 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
8 | HG01943.hp2 HG01975.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1037-5130C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222693 | |||||||
| chr11:89222738 | TA | T | 11 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0077 others(8): Show |
11 | HG02615.hp1 HG02922.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.1037-5073delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89222738 | ||||||
| chr11:89222796 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-5027T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222796 | |||||||
| chr11:89222926 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1037-4897C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222926 | |||||||
| chr11:89222987 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-4836G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89222987 | |||||||
| chr11:89223303 | G | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-4520G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89223303 | |||||||
| chr11:89223325 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.1037-4498A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89223325 | |||||||
| chr11:89223552 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1037-4271G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89223552 | |||||||
| chr11:89223653 | G | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-4170G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89223653 | |||||||
| chr11:89223879 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1037-3944G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89223879 | |||||||
| chr11:89223908 | G | GTT | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0220 others(3): Show |
6 | HG00099.hp2 HG01978.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-3903_1037-390 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89223908 | ||||||
| chr11:89223908 | G | GTTT | 55 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0070 others(52): Show |
56 | HG01074.hp2 HG01099.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1037-3904_1037-390 others(7): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89223908 | ||||||
| chr11:89223908 | G | GTTTT | 17 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0115 others(14): Show |
17 | HG01358.hp2 HG01978.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1037-3905_1037-390 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89223908 | ||||||
| chr11:89223908 | GT | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1037-3902delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89223908 | ||||||
| chr11:89223908 | GTT | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0003c0003t0001g0003 others(2): Show |
6 | HG01192.hp1 HG01515.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-3903_1037-390 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89223908 | ||||||
| chr11:89224022 | G | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(90): Show |
94 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1037-3801G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224022 | |||||||
| chr11:89224023 | G | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0179 |
3 | NA18973.hp2 NA19088.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1037-3800G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224023 | |||||||
| chr11:89224126 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1037-3697C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224126 | |||||||
| chr11:89224217 | C | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(80): Show |
84 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1037-3606C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224217 | |||||||
| chr11:89224318 | T | A | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1037-3505T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224318 | |||||||
| chr11:89224376 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1037-3447A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224376 | |||||||
| chr11:89224522 | A | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1037-3301A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224522 | |||||||
| chr11:89224523 | A | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1037-3300A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224523 | |||||||
| chr11:89224793 | A | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(82): Show |
86 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.1037-3030A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224793 | |||||||
| chr11:89224840 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-2983G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224840 | |||||||
| chr11:89224845 | T | C | 7 | a0001c0001t0001g0118 a0001c0004t0001g0283 a0001c0004t0001g0284 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-2978T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224845 | |||||||
| chr11:89224929 | A | AAT | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-2894_1037-289 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224929 | |||||||
| chr11:89224929 | A | AT | 62 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
65 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1037-2883dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89224929 | ||||||
| chr11:89224929 | AT | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(75): Show |
79 | HG00099.hp2 HG01243.hp1 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.1037-2883delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89224929 | ||||||
| chr11:89224929 | ATT | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-2884_1037-288 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89224929 | ||||||
| chr11:89224938 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0001g0235 others(35): Show |
40 | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1037-2885T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89224938 | |||||||
| chr11:89225373 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1037-2450C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89225373 | |||||||
| chr11:89225717 | G | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-2106G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89225717 | |||||||
| chr11:89225774 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1037-2049G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89225774 | |||||||
| chr11:89225780 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.1037-2043A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89225780 | |||||||
| chr11:89225787 | GA | G | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037-2032delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89225787 | ||||||
| chr11:89225795 | T | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0070 others(46): Show |
50 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(47): Show |
intron_variant | MODIFIER | c.1037-2028T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89225795 | |||||||
| chr11:89226042 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1037-1781T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226042 | |||||||
| chr11:89226049 | T | TACTTTAA others(17): Show |
1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-1753_1037-173 others(28): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89226049 | ||||||
| chr11:89226121 | G | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(80): Show |
84 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(81): Show |
intron_variant | MODIFIER | c.1037-1702G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226121 | |||||||
| chr11:89226169 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-1654A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226169 | |||||||
| chr11:89226189 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-1634G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226189 | |||||||
| chr11:89226260 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(90): Show |
94 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1037-1563T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226260 | |||||||
| chr11:89226264 | T | C | 90 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(87): Show |
91 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.1037-1559T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226264 | |||||||
| chr11:89226365 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-1458T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226365 | |||||||
| chr11:89226458 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1037-1365T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226458 | |||||||
| chr11:89226503 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-1320G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226503 | |||||||
| chr11:89226612 | T | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-1211T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226612 | |||||||
| chr11:89226754 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-1069G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226754 | |||||||
| chr11:89226979 | G | A | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1037-844G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226979 | |||||||
| chr11:89226997 | T | C | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1037-826T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89226997 | |||||||
| chr11:89227028 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1037-795C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227028 | |||||||
| chr11:89227055 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1037-768T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227055 | |||||||
| chr11:89227377 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037-446C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227377 | |||||||
| chr11:89227548 | C | T | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG01243.hp1 HG02486.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-275C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227548 | |||||||
| chr11:89227622 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(87): Show |
91 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.1037-201G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227622 | |||||||
| chr11:89227648 | T | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1037-175T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227648 | |||||||
| chr11:89227664 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1037-159T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227664 | |||||||
| chr11:89227746 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-77T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227746 | |||||||
| chr11:89227795 | A | AT | 9 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
9 | HG00558.hp1 HG02698.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.1037-21dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | 89227795 | ||||||
| chr11:89227816 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG01978.hp2 | splice_region_variant&intron_variant | LOW | c.1037-7T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 2/4 | chr11 | 89227816 | |||||||
| chr11:89227997 | C | T | 2 | a0002c0002t0001g0188 a0002c0002t0001g0190 |
2 | HG00280.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1184+27C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89227997 | |||||||
| chr11:89228003 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+33C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228003 | |||||||
| chr11:89228020 | G | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.1184+50G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228020 | |||||||
| chr11:89228131 | T | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+161T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228131 | |||||||
| chr11:89228281 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1184+311T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228281 | |||||||
| chr11:89228353 | A | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(87): Show |
91 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.1184+383A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228353 | |||||||
| chr11:89228513 | T | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+543T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228513 | |||||||
| chr11:89228619 | T | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1184+649T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228619 | |||||||
| chr11:89228651 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1184+681A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228651 | |||||||
| chr11:89228759 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1184+789C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228759 | |||||||
| chr11:89228922 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0001g0235 others(39): Show |
44 | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1184+952C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228922 | |||||||
| chr11:89228940 | C | A | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1184+970C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228940 | |||||||
| chr11:89228948 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1184+978C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89228948 | |||||||
| chr11:89229180 | G | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+1210G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229180 | |||||||
| chr11:89229274 | TG | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+1305delG | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229274 | |||||||
| chr11:89229335 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1184+1365T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229335 | |||||||
| chr11:89229350 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+1380G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229350 | |||||||
| chr11:89229411 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1184+1441G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229411 | |||||||
| chr11:89229411 | G | T | 84 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0070 others(81): Show |
85 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(82): Show |
intron_variant | MODIFIER | c.1184+1441G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229411 | |||||||
| chr11:89229437 | G | A | 5 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00099.hp2 HG01978.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+1467G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229437 | |||||||
| chr11:89229471 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+1501C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229471 | |||||||
| chr11:89229479 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1184+1509A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229479 | |||||||
| chr11:89229562 | A | AAC | 7 | a0001c0001t0001g0222 a0001c0004t0001g0283 a0001c0004t0001g0284 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184+1593_1184+159 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89229562 | ||||||
| chr11:89229563 | A | AC | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(75): Show |
79 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(76): Show |
intron_variant | MODIFIER | c.1184+1593_1184+159 others(5): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229563 | |||||||
| chr11:89229569 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(87): Show |
91 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.1184+1599G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229569 | |||||||
| chr11:89229657 | A | G | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1184+1687A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229657 | |||||||
| chr11:89229763 | C | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(90): Show |
94 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1184+1793C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229763 | |||||||
| chr11:89229773 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1184+1803C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229773 | |||||||
| chr11:89229786 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.1184+1816C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229786 | |||||||
| chr11:89229794 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0001g0235 others(39): Show |
44 | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1184+1824C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229794 | |||||||
| chr11:89229949 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1184+1979G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229949 | |||||||
| chr11:89229964 | C | G | 50 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0070 others(47): Show |
51 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(48): Show |
intron_variant | MODIFIER | c.1184+1994C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89229964 | |||||||
| chr11:89230023 | C | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+2053C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230023 | |||||||
| chr11:89230054 | C | T | 7 | a0001c0001t0001g0118 a0001c0004t0001g0283 a0001c0004t0001g0284 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2084C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230054 | |||||||
| chr11:89230185 | T | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(82): Show |
86 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.1184+2215T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230185 | |||||||
| chr11:89230189 | T | C | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+2219T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230189 | |||||||
| chr11:89230318 | G | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0276 |
3 | HG01346.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+2348G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230318 | |||||||
| chr11:89230430 | G | T | 1 | a0003c0003t0001g0023 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1184+2460G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230430 | |||||||
| chr11:89230451 | T | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.1184+2481T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230451 | |||||||
| chr11:89230464 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+2494G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230464 | |||||||
| chr11:89230491 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0146 |
2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1184+2521A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230491 | |||||||
| chr11:89230607 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+2637G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230607 | |||||||
| chr11:89230610 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1184+2640A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230610 | |||||||
| chr11:89230657 | A | T | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1184+2687A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230657 | |||||||
| chr11:89230669 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1184+2699C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230669 | |||||||
| chr11:89230750 | T | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+2780T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230750 | |||||||
| chr11:89230906 | T | TA | 12 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0077 others(9): Show |
12 | HG01243.hp2 HG02109.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1184+2950dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89230906 | ||||||
| chr11:89230906 | T | TAA | 66 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0070 others(63): Show |
67 | HG00099.hp2 HG01074.hp2 HG01358.hp2 others(64): Show |
intron_variant | MODIFIER | c.1184+2949_1184+295 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89230906 | ||||||
| chr11:89230906 | T | TAAA | 11 | a0001c0001t0001g0067 a0001c0001t0001g0214 a0001c0001t0001g0215 others(8): Show |
11 | HG01099.hp1 HG01243.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1184+2948_1184+295 others(7): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89230906 | ||||||
| chr11:89230944 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1184+2974G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89230944 | |||||||
| chr11:89231031 | G | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(90): Show |
94 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1184+3061G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231031 | |||||||
| chr11:89231032 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1184+3062G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231032 | |||||||
| chr11:89231038 | G | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+3068G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231038 | |||||||
| chr11:89231079 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+3109G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231079 | |||||||
| chr11:89231094 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(90): Show |
94 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.1184+3124T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231094 | |||||||
| chr11:89231165 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1184+3195C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231165 | |||||||
| chr11:89231167 | T | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG00597.hp1 NA18983.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+3197T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231167 | |||||||
| chr11:89231170 | C | CA | 93 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0015 others(90): Show |
94 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1184+3221dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89231170 | ||||||
| chr11:89231170 | C | CAA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0290 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+3220_1184+322 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89231170 | ||||||
| chr11:89231170 | CA | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0068 a0001c0001t0001g0069 others(8): Show |
11 | HG00639.hp1 HG01167.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+3221delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89231170 | ||||||
| chr11:89231206 | T | TGC | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(159): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1184+3236_1184+323 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231206 | |||||||
| chr11:89231314 | ATGTATCG others(3441): Show |
A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG01243.hp1 HG01358.hp2 others(70): Show |
intron_variant | MODIFIER | c.1184+3348_1184+679 others(4): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89231314 | ||||||
| chr11:89231336 | C | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+3366C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231336 | |||||||
| chr11:89231406 | C | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+3436C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231406 | |||||||
| chr11:89231509 | G | C | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG01074.hp2 HG01099.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184+3539G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231509 | |||||||
| chr11:89231512 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+3542T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231512 | |||||||
| chr11:89231702 | G | A | 6 | a0001c0001t0001g0177 a0001c0001t0001g0254 a0001c0001t0001g0270 others(3): Show |
6 | HG00597.hp1 HG03688.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+3732G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231702 | |||||||
| chr11:89231710 | G | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00609.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1184+3740G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231710 | |||||||
| chr11:89231838 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1184+3868C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231838 | |||||||
| chr11:89231943 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1184+3973C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89231943 | |||||||
| chr11:89231984 | C | CA | 6 | a0001c0001t0001g0122 a0001c0001t0001g0202 a0001c0001t0001g0203 others(3): Show |
6 | HG01346.hp2 HG02040.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+4031dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89231984 | ||||||
| chr11:89231984 | CA | C | 8 | a0001c0001t0001g0174 a0001c0001t0001g0277 a0001c0001t0001g0278 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+4031delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89231984 | ||||||
| chr11:89232028 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1184+4058G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89232028 | |||||||
| chr11:89232392 | C | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1184+4422C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89232392 | |||||||
| chr11:89232463 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+4493G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89232463 | |||||||
| chr11:89232490 | A | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0068 a0001c0001t0001g0069 others(14): Show |
17 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184+4520A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89232490 | |||||||
| chr11:89232758 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
85 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1184+4788T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89232758 | |||||||
| chr11:89232890 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1184+4920G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89232890 | |||||||
| chr11:89233108 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1184+5138G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233108 | |||||||
| chr11:89233254 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+5284G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233254 | |||||||
| chr11:89233271 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+5301C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233271 | |||||||
| chr11:89233414 | C | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+5444C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233414 | |||||||
| chr11:89233416 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1184+5446A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233416 | |||||||
| chr11:89233480 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1184+5510C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233480 | |||||||
| chr11:89233587 | A | G | 11 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(8): Show |
11 | HG01074.hp2 HG01099.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+5617A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233587 | |||||||
| chr11:89233601 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1184+5631T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233601 | |||||||
| chr11:89233630 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1184+5660C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233630 | |||||||
| chr11:89233653 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1184+5683T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233653 | |||||||
| chr11:89233683 | A | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1184+5713A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89233683 | |||||||
| chr11:89233870 | A | ATGGCCC | 89 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
92 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1184+5903_1184+590 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89233870 | ||||||
| chr11:89234071 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1184+6101A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234071 | |||||||
| chr11:89234374 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1184+6404A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234374 | |||||||
| chr11:89234494 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1184+6524A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234494 | |||||||
| chr11:89234748 | T | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+6778T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234748 | |||||||
| chr11:89234822 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(151): Show |
158 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1184+6852T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234822 | |||||||
| chr11:89234824 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1184+6854T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234824 | |||||||
| chr11:89234848 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1184+6878A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234848 | |||||||
| chr11:89234892 | CAT | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+6923_1184+692 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234892 | |||||||
| chr11:89234915 | A | G | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+6945A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89234915 | |||||||
| chr11:89234974 | T | TA | 17 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
17 | HG00423.hp1 HG00423.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184+7018dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89234974 | ||||||
| chr11:89234974 | TA | T | 6 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+7018delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89234974 | ||||||
| chr11:89235094 | T | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+7124T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89235094 | |||||||
| chr11:89235604 | C | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+7634C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89235604 | |||||||
| chr11:89235692 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+7722G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89235692 | |||||||
| chr11:89235719 | TA | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+7750delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89235719 | |||||||
| chr11:89235804 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+7834T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89235804 | |||||||
| chr11:89235898 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1184+7928C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89235898 | |||||||
| chr11:89235911 | A | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+7941A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89235911 | |||||||
| chr11:89236083 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+8113T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236083 | |||||||
| chr11:89236095 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+8125G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236095 | |||||||
| chr11:89236149 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+8179G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236149 | |||||||
| chr11:89236151 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1184+8181A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236151 | |||||||
| chr11:89236176 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1184+8206C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236176 | |||||||
| chr11:89236219 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1184+8249C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236219 | |||||||
| chr11:89236235 | T | TAC | 61 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
62 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(59): Show |
intron_variant | MODIFIER | c.1184+8286_1184+828 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89236235 | ||||||
| chr11:89236235 | T | TACAC | 55 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(52): Show |
58 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1184+8284_1184+828 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89236235 | ||||||
| chr11:89236361 | C | G | 1 | a0001c0001t0001g0113 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1184+8391C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236361 | |||||||
| chr11:89236458 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1184+8488T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236458 | |||||||
| chr11:89236542 | TG | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+8573delG | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236542 | |||||||
| chr11:89236606 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
85 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1184+8636T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236606 | |||||||
| chr11:89236659 | T | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1184+8689T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236659 | |||||||
| chr11:89236838 | A | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1184+8868A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236838 | |||||||
| chr11:89236906 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+8936T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236906 | |||||||
| chr11:89236970 | T | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
103 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1184+9000T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236970 | |||||||
| chr11:89236974 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+9004G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89236974 | |||||||
| chr11:89237296 | C | A | 1 | a0001c0001t0001g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1184+9326C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237296 | |||||||
| chr11:89237305 | C | A | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1184+9335C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237305 | |||||||
| chr11:89237388 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG00558.hp1 NA18992.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1184+9418A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237388 | |||||||
| chr11:89237733 | G | C | 1 | a0001c0001t0001g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1184+9763G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237733 | |||||||
| chr11:89237828 | T | TTTTA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+9878_1184+988 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89237828 | ||||||
| chr11:89237828 | TTTTA | T | 19 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0118 others(16): Show |
19 | HG01243.hp1 HG01243.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+9878_1184+988 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89237828 | ||||||
| chr11:89237867 | A | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
103 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1184+9897A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237867 | |||||||
| chr11:89237938 | C | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+9968C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237938 | |||||||
| chr11:89237966 | G | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(51): Show |
57 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1184+9996G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237966 | |||||||
| chr11:89237989 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG00558.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1184+10019C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89237989 | |||||||
| chr11:89238083 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+10113G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238083 | |||||||
| chr11:89238101 | C | T | 54 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(51): Show |
57 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1184+10131C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238101 | |||||||
| chr11:89238126 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+10156C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238126 | |||||||
| chr11:89238133 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+10163C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238133 | |||||||
| chr11:89238205 | A | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
102 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1184+10235A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238205 | |||||||
| chr11:89238258 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1184+10288T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238258 | |||||||
| chr11:89238310 | G | C | 5 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00099.hp2 HG01978.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+10340G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238310 | |||||||
| chr11:89238452 | C | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0213 others(15): Show |
18 | HG01243.hp1 HG01358.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184+10482C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238452 | |||||||
| chr11:89238470 | T | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
102 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1184+10500T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238470 | |||||||
| chr11:89238516 | C | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
102 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1184+10546C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238516 | |||||||
| chr11:89238536 | G | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
96 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1184+10566G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238536 | |||||||
| chr11:89238609 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1184+10639G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238609 | |||||||
| chr11:89238617 | G | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+10647G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238617 | |||||||
| chr11:89238652 | C | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1184+10682C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238652 | |||||||
| chr11:89238696 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1184+10726C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238696 | |||||||
| chr11:89238950 | C | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(51): Show |
57 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1184+10980C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238950 | |||||||
| chr11:89238964 | C | A | 1 | a0001c0001t0001g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1184+10994C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89238964 | |||||||
| chr11:89239119 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1184+11149G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239119 | |||||||
| chr11:89239178 | C | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
96 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1184+11208C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239178 | |||||||
| chr11:89239218 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1184+11248C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239218 | |||||||
| chr11:89239292 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+11322T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239292 | |||||||
| chr11:89239374 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1184+11404C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239374 | |||||||
| chr11:89239394 | G | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
96 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1184+11424G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239394 | |||||||
| chr11:89239482 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+11512A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239482 | |||||||
| chr11:89239515 | G | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+11545G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239515 | |||||||
| chr11:89239665 | T | G | 18 | a0001c0001t0001g0015 a0001c0001t0001g0118 a0001c0001t0001g0213 others(15): Show |
18 | HG01243.hp1 HG01243.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1184+11695T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239665 | |||||||
| chr11:89239682 | A | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+11712A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239682 | |||||||
| chr11:89239705 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+11735T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239705 | |||||||
| chr11:89239753 | T | C | 8 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0004t0001g0283 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184+11783T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239753 | |||||||
| chr11:89239788 | A | C | 153 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(150): Show |
157 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1184+11818A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239788 | |||||||
| chr11:89239849 | G | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0289 others(6): Show |
9 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+11879G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239849 | |||||||
| chr11:89239874 | A | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0163 |
2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1184+11904A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239874 | |||||||
| chr11:89239938 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+11968C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239938 | |||||||
| chr11:89239999 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1184+12029C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89239999 | |||||||
| chr11:89240033 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
101 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1184+12063C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240033 | |||||||
| chr11:89240040 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+12070C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240040 | |||||||
| chr11:89240041 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+12071G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240041 | |||||||
| chr11:89240076 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1184+12106T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240076 | |||||||
| chr11:89240193 | G | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(51): Show |
57 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1184+12223G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240193 | |||||||
| chr11:89240338 | AT | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+12369delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240338 | |||||||
| chr11:89240387 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1184+12417A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240387 | |||||||
| chr11:89240442 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0070 others(52): Show |
56 | HG00099.hp2 HG01516.hp1 HG01884.hp2 others(53): Show |
intron_variant | MODIFIER | c.1184+12472A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240442 | |||||||
| chr11:89240537 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1184+12567C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240537 | |||||||
| chr11:89240730 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+12760T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240730 | |||||||
| chr11:89240906 | C | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+12936C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240906 | |||||||
| chr11:89240967 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1184+12997G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89240967 | |||||||
| chr11:89241046 | C | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1184+13076C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241046 | |||||||
| chr11:89241155 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0064 |
2 | NA18946.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1184+13185T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241155 | |||||||
| chr11:89241311 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1184+13341G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241311 | |||||||
| chr11:89241467 | G | T | 1 | a0001c0001t0001g0294 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1184+13497G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241467 | |||||||
| chr11:89241539 | A | G | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(121): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1184+13569A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241539 | |||||||
| chr11:89241708 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0265 |
2 | NA18990.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1184+13738G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241708 | |||||||
| chr11:89241712 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1184+13742T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241712 | |||||||
| chr11:89241828 | CAT | C | 3 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0178 |
3 | HG00423.hp1 NA19001.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1184+13867_1184+13 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89241828 | ||||||
| chr11:89241842 | A | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+13872A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241842 | |||||||
| chr11:89241930 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+13960A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241930 | |||||||
| chr11:89241939 | C | T | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+13969C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241939 | |||||||
| chr11:89241951 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1184+13981A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89241951 | |||||||
| chr11:89242248 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1184+14278T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242248 | |||||||
| chr11:89242283 | C | T | 29 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0118 others(26): Show |
29 | HG01074.hp2 HG01099.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1184+14313C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242283 | |||||||
| chr11:89242307 | A | C | 5 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00099.hp2 HG01978.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+14337A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242307 | |||||||
| chr11:89242382 | AT | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+14421delT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89242382 | ||||||
| chr11:89242384 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1184+14414T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242384 | |||||||
| chr11:89242499 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1184+14529T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242499 | |||||||
| chr11:89242508 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1184+14538C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242508 | |||||||
| chr11:89242574 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1184+14604T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242574 | |||||||
| chr11:89242601 | C | A | 29 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0118 others(26): Show |
29 | HG01074.hp2 HG01099.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1184+14631C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242601 | |||||||
| chr11:89242747 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+14777T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242747 | |||||||
| chr11:89242945 | T | C | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(146): Show |
153 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1184+14975T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242945 | |||||||
| chr11:89242989 | T | C | 16 | a0002c0002t0001g0007 a0002c0002t0001g0132 a0002c0002t0001g0136 others(13): Show |
17 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184+15019T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242989 | |||||||
| chr11:89242995 | C | G | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+15025C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89242995 | |||||||
| chr11:89243036 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+15066T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243036 | |||||||
| chr11:89243106 | C | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(9): Show |
12 | HG01074.hp2 HG01099.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1184+15136C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243106 | |||||||
| chr11:89243115 | G | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(146): Show |
153 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1184+15145G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243115 | |||||||
| chr11:89243141 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0178 |
3 | HG00423.hp1 NA19001.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1184+15171G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243141 | |||||||
| chr11:89243308 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+15338G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243308 | |||||||
| chr11:89243449 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1184+15479C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243449 | |||||||
| chr11:89243546 | T | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(8): Show |
11 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1184+15576T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243546 | |||||||
| chr11:89243601 | A | ATCACATC others(28): Show |
1 | a0001c0001t0001g0169 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1184+15632_1184+15 others(41): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89243601 | ||||||
| chr11:89243765 | T | C | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+15795T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243765 | |||||||
| chr11:89243795 | T | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0118 others(16): Show |
19 | HG01243.hp1 HG01243.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+15825T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89243795 | |||||||
| chr11:89244001 | C | T | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+16031C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244001 | |||||||
| chr11:89244035 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1184+16065C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244035 | |||||||
| chr11:89244144 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+16174A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244144 | |||||||
| chr11:89244196 | G | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(51): Show |
57 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1184+16226G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244196 | |||||||
| chr11:89244265 | A | C | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+16295A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244265 | |||||||
| chr11:89244293 | C | G | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+16323C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244293 | |||||||
| chr11:89244301 | A | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1184+16331A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244301 | |||||||
| chr11:89244305 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1184+16335C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244305 | |||||||
| chr11:89244329 | C | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1184+16359C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244329 | |||||||
| chr11:89244347 | T | C | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(146): Show |
153 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1184+16377T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244347 | |||||||
| chr11:89244404 | C | T | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+16434C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244404 | |||||||
| chr11:89244418 | C | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1184+16448C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244418 | |||||||
| chr11:89244439 | C | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(115): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1184+16469C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244439 | |||||||
| chr11:89244508 | A | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG00099.hp2 HG01978.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1184+16538A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244508 | |||||||
| chr11:89244635 | G | A | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+16665G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244635 | |||||||
| chr11:89244739 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1184+16769C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244739 | |||||||
| chr11:89244806 | A | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+16836A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244806 | |||||||
| chr11:89244872 | C | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+16902C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244872 | |||||||
| chr11:89244884 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1184+16914T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244884 | |||||||
| chr11:89244964 | A | G | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+16994A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89244964 | |||||||
| chr11:89245097 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+17127A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245097 | |||||||
| chr11:89245103 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1184+17133G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245103 | |||||||
| chr11:89245140 | G | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(116): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1184+17170G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245140 | |||||||
| chr11:89245199 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1184+17229T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245199 | |||||||
| chr11:89245368 | T | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(2): Show |
5 | HG02615.hp1 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+17398T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245368 | |||||||
| chr11:89245377 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1184+17407A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245377 | |||||||
| chr11:89245430 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1184+17460G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245430 | |||||||
| chr11:89245444 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1184+17474T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245444 | |||||||
| chr11:89245459 | T | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
52 | HG01516.hp1 HG01884.hp2 HG02055.hp2 others(49): Show |
intron_variant | MODIFIER | c.1184+17489T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245459 | |||||||
| chr11:89245577 | T | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+17607T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245577 | |||||||
| chr11:89245696 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1184+17726G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245696 | |||||||
| chr11:89245754 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1184+17784C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245754 | |||||||
| chr11:89245774 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+17804T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245774 | |||||||
| chr11:89245823 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0163 |
2 | HG02683.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1184+17853G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245823 | |||||||
| chr11:89245918 | C | T | 1 | a0003c0003t0001g0024 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1184+17948C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245918 | |||||||
| chr11:89245920 | C | CA | 6 | a0001c0001t0001g0045 a0001c0001t0001g0063 a0001c0001t0001g0144 others(3): Show |
6 | HG00140.hp2 HG02083.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+17962dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89245920 | ||||||
| chr11:89245920 | CA | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
98 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.1184+17962delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89245920 | ||||||
| chr11:89245928 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1184+17958A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245928 | |||||||
| chr11:89245929 | A | C | 99 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(96): Show |
101 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1184+17959A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89245929 | |||||||
| chr11:89246078 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1184+18108G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246078 | |||||||
| chr11:89246163 | A | AG | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(137): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1184+18193_1184+18 others(7): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246163 | |||||||
| chr11:89246164 | A | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(137): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1184+18194A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246164 | |||||||
| chr11:89246166 | A | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(137): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1184+18196A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246166 | |||||||
| chr11:89246323 | T | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
77 | HG00621.hp1 HG01243.hp1 HG01243.hp2 others(74): Show |
intron_variant | MODIFIER | c.1184+18353T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246323 | |||||||
| chr11:89246441 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1184+18471G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246441 | |||||||
| chr11:89246482 | T | C | 18 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0096 others(15): Show |
18 | HG01243.hp1 HG01358.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184+18512T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246482 | |||||||
| chr11:89246563 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1184+18593A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246563 | |||||||
| chr11:89246678 | T | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(153): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1184+18708T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246678 | |||||||
| chr11:89246719 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1184+18749T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246719 | |||||||
| chr11:89246724 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1184+18754A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246724 | |||||||
| chr11:89246749 | A | C | 2 | a0001c0006t0001g0082 a0001c0006t0001g0083 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1184+18779A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246749 | |||||||
| chr11:89246757 | C | A | 11 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0123 others(8): Show |
11 | HG01074.hp2 HG01099.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+18787C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246757 | |||||||
| chr11:89246787 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0071 others(30): Show |
34 | HG00621.hp1 HG01978.hp2 HG02165.hp1 others(31): Show |
intron_variant | MODIFIER | c.1184+18817T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246787 | |||||||
| chr11:89246862 | A | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+18892A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89246862 | |||||||
| chr11:89247092 | G | A | 101 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
102 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1184+19122G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89247092 | |||||||
| chr11:89247291 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0180 |
2 | NA18978.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1184+19321A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89247291 | |||||||
| chr11:89247419 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1184+19449T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89247419 | |||||||
| chr11:89247483 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02165.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1184+19513C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89247483 | |||||||
| chr11:89247526 | G | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+19556G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89247526 | |||||||
| chr11:89247639 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184+19669C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89247639 | |||||||
| chr11:89247741 | A | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
6 | HG01346.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+19771A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89247741 | |||||||
| chr11:89248148 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1184+20178G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248148 | |||||||
| chr11:89248335 | T | C | 26 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0096 others(23): Show |
26 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1184+20365T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248335 | |||||||
| chr11:89248438 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1184+20468G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248438 | |||||||
| chr11:89248517 | T | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01346.hp2 HG02615.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+20547T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248517 | |||||||
| chr11:89248571 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1184+20601G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248571 | |||||||
| chr11:89248590 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1184+20620G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248590 | |||||||
| chr11:89248618 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1184+20648G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248618 | |||||||
| chr11:89248645 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1184+20675T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248645 | |||||||
| chr11:89248668 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1184+20698T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89248668 | |||||||
| chr11:89249027 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0114 |
2 | NA18944.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1184+21057T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249027 | |||||||
| chr11:89249364 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1184+21394A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249364 | |||||||
| chr11:89249374 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1184+21404C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249374 | |||||||
| chr11:89249411 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1184+21441G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249411 | |||||||
| chr11:89249471 | C | CA | 103 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1184+21520dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89249471 | ||||||
| chr11:89249471 | C | CAA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(14): Show |
18 | HG00140.hp1 HG00741.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1184+21519_1184+21 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89249471 | ||||||
| chr11:89249471 | C | CAAAA | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+21517_1184+21 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89249471 | ||||||
| chr11:89249550 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1184+21580T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249550 | |||||||
| chr11:89249552 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(9): Show |
12 | HG01346.hp2 HG01884.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1184+21582G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249552 | |||||||
| chr11:89249566 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(1): Show |
4 | HG01346.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+21596C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249566 | |||||||
| chr11:89249652 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(1): Show |
4 | HG01346.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+21682A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249652 | |||||||
| chr11:89249725 | G | A | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+21755G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249725 | |||||||
| chr11:89249835 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(48): Show |
51 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1184+21865T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249835 | |||||||
| chr11:89249924 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1184+21954C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89249924 | |||||||
| chr11:89250026 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1184+22056G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250026 | |||||||
| chr11:89250299 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1184+22329C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250299 | |||||||
| chr11:89250346 | G | A | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+22376G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250346 | |||||||
| chr11:89250464 | C | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0096 others(23): Show |
26 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1184+22494C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250464 | |||||||
| chr11:89250683 | C | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(1): Show |
4 | HG01346.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+22713C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250683 | |||||||
| chr11:89250740 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1184+22770C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250740 | |||||||
| chr11:89250806 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+22836C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250806 | |||||||
| chr11:89250867 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+22897G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250867 | |||||||
| chr11:89250911 | C | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(1): Show |
4 | HG01346.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+22941C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89250911 | |||||||
| chr11:89251207 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+23237T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251207 | |||||||
| chr11:89251272 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(1): Show |
4 | HG01346.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+23302G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251272 | |||||||
| chr11:89251459 | C | A | 1 | a0001c0006t0001g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1184+23489C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251459 | |||||||
| chr11:89251544 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1184+23574A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251544 | |||||||
| chr11:89251658 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1184+23688C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251658 | |||||||
| chr11:89251696 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+23726G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251696 | |||||||
| chr11:89251706 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+23736A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251706 | |||||||
| chr11:89251816 | C | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0096 others(23): Show |
26 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1184+23846C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251816 | |||||||
| chr11:89251853 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+23883C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251853 | |||||||
| chr11:89251889 | T | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+23919T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251889 | |||||||
| chr11:89251967 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+23997T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89251967 | |||||||
| chr11:89252029 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1184+24059A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89252029 | |||||||
| chr11:89252186 | G | T | 33 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0070 others(30): Show |
33 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1184+24216G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89252186 | |||||||
| chr11:89252198 | TCCCTTGA others(11): Show |
T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+24231_1184+24 others(24): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89252198 | ||||||
| chr11:89252526 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1184+24556T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89252526 | |||||||
| chr11:89252680 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1184+24710T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89252680 | |||||||
| chr11:89252772 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
108 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1184+24802C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89252772 | |||||||
| chr11:89252796 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1184+24826G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89252796 | |||||||
| chr11:89252906 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+24936T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89252906 | |||||||
| chr11:89253115 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1184+25145C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253115 | |||||||
| chr11:89253274 | T | G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(6): Show |
9 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+25304T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253274 | |||||||
| chr11:89253292 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1184+25322A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253292 | |||||||
| chr11:89253537 | G | A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1184+25567G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253537 | |||||||
| chr11:89253620 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1184+25650T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253620 | |||||||
| chr11:89253643 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0177 a0001c0001t0001g0204 others(1): Show |
4 | HG00558.hp2 HG00597.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+25673T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253643 | |||||||
| chr11:89253699 | CATTT | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(68): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1184+25732_1184+25 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89253699 | ||||||
| chr11:89253781 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+25811T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253781 | |||||||
| chr11:89253876 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1184+25906C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253876 | |||||||
| chr11:89253994 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1184+26024G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89253994 | |||||||
| chr11:89254036 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1184+26066G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254036 | |||||||
| chr11:89254257 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1184+26287G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254257 | |||||||
| chr11:89254325 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1184+26355G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254325 | |||||||
| chr11:89254330 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1184+26360A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254330 | |||||||
| chr11:89254373 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0067 others(43): Show |
47 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(44): Show |
intron_variant | MODIFIER | c.1184+26403C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254373 | |||||||
| chr11:89254412 | G | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0071 others(28): Show |
32 | HG00621.hp1 HG01978.hp2 HG02165.hp1 others(29): Show |
intron_variant | MODIFIER | c.1184+26442G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254412 | |||||||
| chr11:89254419 | G | A | 2 | a0001c0001t0001g0008 a0001c0008t0001g0008 |
2 | NA18968.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1184+26449G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254419 | |||||||
| chr11:89254498 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1184+26528G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254498 | |||||||
| chr11:89254505 | T | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(175): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1184+26535T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254505 | |||||||
| chr11:89254571 | A | T | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1184+26601A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254571 | |||||||
| chr11:89254585 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1184+26615C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254585 | |||||||
| chr11:89254625 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184+26655T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254625 | |||||||
| chr11:89254791 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1184+26821T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89254791 | |||||||
| chr11:89255007 | G | A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1184+27037G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255007 | |||||||
| chr11:89255049 | C | T | 1 | a0001c0006t0001g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1184+27079C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255049 | |||||||
| chr11:89255069 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1184+27099T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255069 | |||||||
| chr11:89255255 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1184+27285G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255255 | |||||||
| chr11:89255359 | G | T | 2 | a0001c0004t0001g0284 a0001c0004t0001g0285 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1184+27389G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255359 | |||||||
| chr11:89255367 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(5): Show |
8 | HG01346.hp2 HG01884.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184+27397A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255367 | |||||||
| chr11:89255396 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(5): Show |
8 | HG01346.hp2 HG01884.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184+27426A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255396 | |||||||
| chr11:89255768 | T | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(6): Show |
9 | HG01346.hp2 HG01884.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+27798T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255768 | |||||||
| chr11:89255817 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+27847A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255817 | |||||||
| chr11:89255834 | T | A | 1 | a0002c0002t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1184+27864T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255834 | |||||||
| chr11:89255910 | T | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0144 a0001c0001t0001g0151 |
3 | HG02083.hp2 NA18945.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1184+27940T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89255910 | |||||||
| chr11:89256060 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(5): Show |
8 | HG01346.hp2 HG01884.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184+28090T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256060 | |||||||
| chr11:89256082 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1184+28112G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256082 | |||||||
| chr11:89256162 | A | C | 1 | a0002c0002t0001g0184 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1184+28192A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256162 | |||||||
| chr11:89256231 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1184+28261C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256231 | |||||||
| chr11:89256245 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1184+28275C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256245 | |||||||
| chr11:89256267 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1184+28297G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256267 | |||||||
| chr11:89256288 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG04184.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+28318G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256288 | |||||||
| chr11:89256467 | ATG | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(163): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1185-28288_1185-28 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89256467 | ||||||
| chr11:89256467 | ATGTG | A | 6 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-28290_1185-28 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89256467 | ||||||
| chr11:89256563 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-28210T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256563 | |||||||
| chr11:89256881 | T | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0103 others(41): Show |
46 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1185-27892T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256881 | |||||||
| chr11:89256973 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1185-27800G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89256973 | |||||||
| chr11:89257063 | C | A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-27710C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257063 | |||||||
| chr11:89257099 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(1): Show |
4 | HG01346.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-27674G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257099 | |||||||
| chr11:89257212 | G | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(46): Show |
49 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1185-27561G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257212 | |||||||
| chr11:89257361 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-27412C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257361 | |||||||
| chr11:89257471 | GTTATATA others(11): Show |
G | 1 | a0001c0001t0001g0183 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1185-27299_1185-27 others(24): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89257471 | ||||||
| chr11:89257475 | T | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0067 others(45): Show |
49 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(46): Show |
intron_variant | MODIFIER | c.1185-27298T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257475 | |||||||
| chr11:89257548 | C | T | 1 | a0002c0002t0001g0211 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1185-27225C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257548 | |||||||
| chr11:89257618 | C | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0096 others(23): Show |
26 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1185-27155C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257618 | |||||||
| chr11:89257641 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-27132A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257641 | |||||||
| chr11:89257678 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1185-27095G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257678 | |||||||
| chr11:89257776 | T | A | 1 | a0001c0006t0001g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1185-26997T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257776 | |||||||
| chr11:89257806 | C | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(46): Show |
49 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1185-26967C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257806 | |||||||
| chr11:89257905 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1185-26868G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257905 | |||||||
| chr11:89257986 | T | A | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(7): Show |
10 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1185-26787T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257986 | |||||||
| chr11:89257987 | A | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(4): Show |
7 | HG01884.hp1 HG02922.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-26786A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89257987 | |||||||
| chr11:89258034 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1185-26739T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258034 | |||||||
| chr11:89258064 | T | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-26709T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258064 | |||||||
| chr11:89258066 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-26707A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258066 | |||||||
| chr11:89258155 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1185-26618G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258155 | |||||||
| chr11:89258237 | A | T | 1 | a0001c0006t0001g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1185-26536A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258237 | |||||||
| chr11:89258339 | A | AT | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-26424dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89258339 | ||||||
| chr11:89258447 | C | CA | 12 | a0001c0001t0001g0063 a0001c0001t0001g0076 a0001c0001t0001g0119 others(9): Show |
12 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-26313dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89258447 | ||||||
| chr11:89258584 | CAT | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-26187_1185-26 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89258584 | ||||||
| chr11:89258658 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1185-26115A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258658 | |||||||
| chr11:89258706 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1185-26067G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258706 | |||||||
| chr11:89258805 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-25968T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258805 | |||||||
| chr11:89258830 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1185-25943A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89258830 | |||||||
| chr11:89259183 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-25590G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89259183 | |||||||
| chr11:89259207 | G | A | 11 | a0001c0001t0001g0242 a0001c0001t0001g0251 a0001c0001t0001g0255 others(8): Show |
11 | HG01256.hp1 HG01346.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1185-25566G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89259207 | |||||||
| chr11:89259478 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0218 others(1): Show |
4 | HG01243.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-25295C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89259478 | |||||||
| chr11:89259532 | G | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(9): Show |
12 | HG01346.hp2 HG01884.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1185-25241G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89259532 | |||||||
| chr11:89259612 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1185-25161C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89259612 | |||||||
| chr11:89259806 | T | C | 1 | a0001c0004t0001g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1185-24967T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89259806 | |||||||
| chr11:89259935 | A | G | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-24838A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89259935 | |||||||
| chr11:89260226 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-24547G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89260226 | |||||||
| chr11:89260248 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1185-24525T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89260248 | |||||||
| chr11:89260250 | C | CA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0092 a0001c0001t0001g0120 others(5): Show |
9 | HG00639.hp1 HG01192.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1185-24508dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89260250 | ||||||
| chr11:89260250 | CA | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(3): Show |
6 | HG01346.hp2 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-24508delA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89260250 | ||||||
| chr11:89260384 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1185-24389G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89260384 | |||||||
| chr11:89260430 | T | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-24343T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89260430 | |||||||
| chr11:89260480 | G | A | 26 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0096 others(23): Show |
26 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1185-24293G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89260480 | |||||||
| chr11:89261132 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(4): Show |
7 | HG01884.hp1 HG02922.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-23641A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89261132 | |||||||
| chr11:89261174 | G | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-23599G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89261174 | |||||||
| chr11:89261197 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0168 a0001c0001t0001g0207 |
3 | HG00544.hp1 HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1185-23576A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89261197 | |||||||
| chr11:89261364 | G | GA | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-23404dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89261364 | ||||||
| chr11:89261579 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0099 |
3 | NA18961.hp2 NA18971.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1185-23194A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89261579 | |||||||
| chr11:89261787 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-22986A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89261787 | |||||||
| chr11:89261811 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1185-22962G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89261811 | |||||||
| chr11:89262066 | A | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-22707A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262066 | |||||||
| chr11:89262093 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0088 a0001c0001t0001g0098 |
3 | HG02055.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1185-22680T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262093 | |||||||
| chr11:89262116 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1185-22657C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262116 | |||||||
| chr11:89262175 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-22598C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262175 | |||||||
| chr11:89262233 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18992.hp1 NA19002.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1185-22540A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262233 | |||||||
| chr11:89262277 | T | C | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG01074.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-22496T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262277 | |||||||
| chr11:89262428 | C | G | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-22345C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262428 | |||||||
| chr11:89262548 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1185-22225A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262548 | |||||||
| chr11:89262570 | A | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0290 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1185-22203A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262570 | |||||||
| chr11:89262595 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1185-22178C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262595 | |||||||
| chr11:89262846 | C | CT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
7 | HG00639.hp1 HG00642.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-21927_1185-21 others(7): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262846 | |||||||
| chr11:89262847 | C | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
7 | HG00639.hp1 HG00642.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-21926C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262847 | |||||||
| chr11:89262847 | C | CA | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(114): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.1185-21901dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89262847 | ||||||
| chr11:89262847 | C | CAA | 21 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0040 others(18): Show |
21 | HG00741.hp2 HG02145.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1185-21902_1185-21 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89262847 | ||||||
| chr11:89262847 | C | CAAA | 43 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0061 others(40): Show |
44 | HG00621.hp1 HG01243.hp2 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.1185-21903_1185-21 others(9): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89262847 | ||||||
| chr11:89262847 | C | CAAAA | 8 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0097 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-21904_1185-21 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89262847 | ||||||
| chr11:89262860 | A | ACAAAC | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-21913_1185-21 others(11): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262860 | |||||||
| chr11:89262860 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1185-21913A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262860 | |||||||
| chr11:89262864 | A | ACAAAC | 3 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02622.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1185-21909_1185-21 others(11): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262864 | |||||||
| chr11:89262864 | A | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-21909A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262864 | |||||||
| chr11:89262871 | AAC | A | 24 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0070 others(21): Show |
24 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1185-21900_1185-21 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89262871 | ||||||
| chr11:89262872 | AC | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0146 a0001c0001t0001g0165 others(4): Show |
7 | HG01978.hp1 HG02683.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-21900delC | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262872 | |||||||
| chr11:89262873 | C | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1185-21900C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262873 | |||||||
| chr11:89262876 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-21897C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262876 | |||||||
| chr11:89262952 | A | G | 1 | a0002c0002t0001g0186 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1185-21821A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262952 | |||||||
| chr11:89262984 | G | C | 28 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0077 others(25): Show |
28 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1185-21789G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89262984 | |||||||
| chr11:89263091 | T | C | 1 | a0001c0006t0001g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1185-21682T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263091 | |||||||
| chr11:89263164 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1185-21609T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263164 | |||||||
| chr11:89263297 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-21476T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263297 | |||||||
| chr11:89263493 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0231 |
2 | HG02040.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1185-21280T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263493 | |||||||
| chr11:89263551 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1185-21222A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263551 | |||||||
| chr11:89263573 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1185-21200T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263573 | |||||||
| chr11:89263714 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1185-21059A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263714 | |||||||
| chr11:89263889 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-20884C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263889 | |||||||
| chr11:89263893 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1185-20880A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263893 | |||||||
| chr11:89263922 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1185-20851G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263922 | |||||||
| chr11:89263930 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1185-20843A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89263930 | |||||||
| chr11:89264049 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1185-20724T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264049 | |||||||
| chr11:89264058 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-20715C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264058 | |||||||
| chr11:89264149 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1185-20624C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264149 | |||||||
| chr11:89264172 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1185-20601T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264172 | |||||||
| chr11:89264243 | A | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-20530A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264243 | |||||||
| chr11:89264352 | A | C | 46 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(43): Show |
46 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1185-20421A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264352 | |||||||
| chr11:89264425 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1185-20348T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264425 | |||||||
| chr11:89264465 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1185-20308G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264465 | |||||||
| chr11:89264728 | A | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0067 others(45): Show |
49 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(46): Show |
intron_variant | MODIFIER | c.1185-20045A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264728 | |||||||
| chr11:89264735 | C | CA | 92 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
93 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1185-20026dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89264735 | ||||||
| chr11:89264735 | C | CAA | 12 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
12 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-20027_1185-20 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89264735 | ||||||
| chr11:89264744 | A | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0101 others(38): Show |
44 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1185-20029A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264744 | |||||||
| chr11:89264748 | C | A | 46 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(43): Show |
46 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1185-20025C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264748 | |||||||
| chr11:89264752 | C | A | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG01243.hp1 HG02486.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-20021C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264752 | |||||||
| chr11:89264834 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-19939T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264834 | |||||||
| chr11:89264962 | C | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(2): Show |
5 | HG01346.hp2 HG01884.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-19811C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89264962 | |||||||
| chr11:89265071 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02622.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1185-19702A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265071 | |||||||
| chr11:89265116 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-19657A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265116 | |||||||
| chr11:89265196 | A | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(5): Show |
8 | HG01346.hp2 HG01884.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-19577A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265196 | |||||||
| chr11:89265214 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1185-19559A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265214 | |||||||
| chr11:89265232 | T | G | 38 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0070 others(35): Show |
38 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1185-19541T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265232 | |||||||
| chr11:89265321 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1185-19452C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265321 | |||||||
| chr11:89265549 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1185-19224T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265549 | |||||||
| chr11:89265703 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1185-19070A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265703 | |||||||
| chr11:89265740 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-19033T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265740 | |||||||
| chr11:89265754 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1185-19019T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89265754 | |||||||
| chr11:89265906 | G | GA | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(4): Show |
7 | HG01884.hp1 HG02922.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-18860dupA | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89265906 | ||||||
| chr11:89266008 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(2): Show |
5 | HG00597.hp2 HG02615.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-18765G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266008 | |||||||
| chr11:89266301 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(5): Show |
8 | HG01346.hp2 HG01884.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-18472A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266301 | |||||||
| chr11:89266336 | G | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
12 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-18437G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266336 | |||||||
| chr11:89266467 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1185-18306G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266467 | |||||||
| chr11:89266520 | C | CCAACAA | 3 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02622.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1185-18237_1185-18 others(12): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89266520 | ||||||
| chr11:89266576 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1185-18197T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266576 | |||||||
| chr11:89266694 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-18079A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266694 | |||||||
| chr11:89266736 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 |
3 | HG02615.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1185-18037A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266736 | |||||||
| chr11:89266786 | GAAAC | G | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-17982_1185-17 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89266786 | ||||||
| chr11:89266828 | A | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(46): Show |
49 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1185-17945A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266828 | |||||||
| chr11:89266945 | T | G | 5 | a0001c0001t0001g0166 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG02129.hp2 NA18940.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-17828T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89266945 | |||||||
| chr11:89267044 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1185-17729C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89267044 | |||||||
| chr11:89267592 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1185-17181G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89267592 | |||||||
| chr11:89267812 | A | ATG | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0027 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-16944_1185-16 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89267812 | ||||||
| chr11:89267873 | A | T | 1 | a0003c0003t0001g0024 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1185-16900A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89267873 | |||||||
| chr11:89267905 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-16868C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89267905 | |||||||
| chr11:89267958 | G | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(63): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1185-16815G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89267958 | |||||||
| chr11:89268031 | T | C | 2 | a0001c0004t0001g0286 a0001c0004t0001g0287 |
2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1185-16742T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89268031 | |||||||
| chr11:89268139 | G | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-16634G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89268139 | |||||||
| chr11:89268453 | G | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(46): Show |
49 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1185-16320G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89268453 | |||||||
| chr11:89268597 | T | C | 5 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG01346.hp2 HG02922.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-16176T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89268597 | |||||||
| chr11:89268877 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1185-15896C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89268877 | |||||||
| chr11:89268889 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-15884C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89268889 | |||||||
| chr11:89268909 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-15864T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89268909 | |||||||
| chr11:89269009 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-15764G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269009 | |||||||
| chr11:89269011 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1185-15762A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269011 | |||||||
| chr11:89269206 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-15567A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269206 | |||||||
| chr11:89269249 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-15524C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269249 | |||||||
| chr11:89269257 | C | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1185-15516C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269257 | |||||||
| chr11:89269261 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1185-15512T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269261 | |||||||
| chr11:89269366 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0296 |
2 | HG00597.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1185-15407T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269366 | |||||||
| chr11:89269398 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1185-15375A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269398 | |||||||
| chr11:89269440 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1185-15333C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269440 | |||||||
| chr11:89269463 | G | GT | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-15304dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89269463 | ||||||
| chr11:89269591 | T | C | 6 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
6 | HG00544.hp1 HG02129.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-15182T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269591 | |||||||
| chr11:89269913 | T | G | 1 | a0001c0001t0002g0208 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1185-14860T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269913 | |||||||
| chr11:89269920 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1185-14853C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269920 | |||||||
| chr11:89269957 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-14816C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269957 | |||||||
| chr11:89269959 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0153 a0001c0001t0001g0296 |
3 | HG00597.hp2 NA18960.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1185-14814T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89269959 | |||||||
| chr11:89270049 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1185-14724C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270049 | |||||||
| chr11:89270108 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1185-14665C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270108 | |||||||
| chr11:89270202 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-14571C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270202 | |||||||
| chr11:89270266 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 |
3 | NA18943.hp2 NA19001.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1185-14507C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270266 | |||||||
| chr11:89270320 | A | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-14453A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270320 | |||||||
| chr11:89270411 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1185-14362C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270411 | |||||||
| chr11:89270436 | C | A | 33 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0070 others(30): Show |
33 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1185-14337C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270436 | |||||||
| chr11:89270528 | A | G | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-14245A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270528 | |||||||
| chr11:89270688 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-14085T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89270688 | |||||||
| chr11:89271366 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1185-13407T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271366 | |||||||
| chr11:89271413 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1185-13360A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271413 | |||||||
| chr11:89271455 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0290 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1185-13318C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271455 | |||||||
| chr11:89271531 | TTCTGGTA others(9): Show |
T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(4): Show |
7 | NA18943.hp2 NA18983.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-13230_1185-13 others(22): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89271531 | ||||||
| chr11:89271588 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-13185G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271588 | |||||||
| chr11:89271646 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1185-13127A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271646 | |||||||
| chr11:89271654 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0289 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1185-13119C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271654 | |||||||
| chr11:89271662 | A | G | 11 | a0001c0001t0001g0063 a0001c0001t0001g0076 a0001c0001t0001g0119 others(8): Show |
11 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1185-13111A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271662 | |||||||
| chr11:89271726 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1185-13047T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271726 | |||||||
| chr11:89271729 | A | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0089 |
2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1185-13044A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271729 | |||||||
| chr11:89271747 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18971.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1185-13026T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271747 | |||||||
| chr11:89271757 | A | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0289 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1185-13016A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271757 | |||||||
| chr11:89271917 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
12 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-12856T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271917 | |||||||
| chr11:89271921 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1185-12852A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89271921 | |||||||
| chr11:89272085 | A | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(63): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1185-12688A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272085 | |||||||
| chr11:89272099 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1185-12674G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272099 | |||||||
| chr11:89272150 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG01081.hp1 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1185-12623C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272150 | |||||||
| chr11:89272167 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1185-12606T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272167 | |||||||
| chr11:89272316 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1185-12457C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272316 | |||||||
| chr11:89272326 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-12447C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272326 | |||||||
| chr11:89272394 | C | CT | 8 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | HG02109.hp2 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-12366dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89272394 | ||||||
| chr11:89272418 | G | T | 32 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0070 others(29): Show |
32 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1185-12355G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272418 | |||||||
| chr11:89272618 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0108 |
2 | NA18992.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1185-12155T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272618 | |||||||
| chr11:89272643 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-12130G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272643 | |||||||
| chr11:89272705 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0108 |
2 | NA18992.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1185-12068T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272705 | |||||||
| chr11:89272749 | C | T | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-12024C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89272749 | |||||||
| chr11:89273024 | C | A | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-11749C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273024 | |||||||
| chr11:89273025 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-11748G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273025 | |||||||
| chr11:89273064 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1185-11709C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273064 | |||||||
| chr11:89273144 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1185-11629A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273144 | |||||||
| chr11:89273167 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0221 |
2 | HG00099.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1185-11606T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273167 | |||||||
| chr11:89273362 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1185-11411A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273362 | |||||||
| chr11:89273411 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-11362C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273411 | |||||||
| chr11:89273597 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1185-11176C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273597 | |||||||
| chr11:89273598 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-11175T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273598 | |||||||
| chr11:89273633 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1185-11140G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273633 | |||||||
| chr11:89273749 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0105 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1185-11024A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273749 | |||||||
| chr11:89273827 | TC | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02622.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1185-10943delC | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89273827 | ||||||
| chr11:89273851 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0105 others(38): Show |
43 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1185-10922T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273851 | |||||||
| chr11:89273895 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-10878G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89273895 | |||||||
| chr11:89274017 | A | AT | 64 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(61): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1185-10754dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 89274017 | ||||||
| chr11:89274076 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-10697G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274076 | |||||||
| chr11:89274344 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-10429C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274344 | |||||||
| chr11:89274411 | C | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
101 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1185-10362C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274411 | |||||||
| chr11:89274431 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1185-10342G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274431 | |||||||
| chr11:89274472 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-10301C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274472 | |||||||
| chr11:89274483 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1185-10290T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274483 | |||||||
| chr11:89274532 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-10241T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274532 | |||||||
| chr11:89274754 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(68): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1185-10019C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274754 | |||||||
| chr11:89274784 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1185-9989C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274784 | |||||||
| chr11:89274792 | T | C | 5 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
5 | HG00423.hp2 HG00558.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-9981T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274792 | |||||||
| chr11:89274840 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0070 others(29): Show |
32 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1185-9933G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274840 | |||||||
| chr11:89274908 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18992.hp1 NA19002.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1185-9865C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89274908 | |||||||
| chr11:89275222 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1185-9551G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275222 | |||||||
| chr11:89275388 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
12 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-9385C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275388 | |||||||
| chr11:89275443 | T | A | 1 | a0001c0001t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1185-9330T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275443 | |||||||
| chr11:89275469 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1185-9304C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275469 | |||||||
| chr11:89275514 | A | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
7 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-9259A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275514 | |||||||
| chr11:89275648 | C | G | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
101 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1185-9125C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275648 | |||||||
| chr11:89275665 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1185-9108G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275665 | |||||||
| chr11:89275858 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1185-8915T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89275858 | |||||||
| chr11:89276008 | C | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-8765C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276008 | |||||||
| chr11:89276187 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1185-8586T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276187 | |||||||
| chr11:89276254 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1185-8519G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276254 | |||||||
| chr11:89276263 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-8510T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276263 | |||||||
| chr11:89276405 | T | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0089 |
2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1185-8368T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276405 | |||||||
| chr11:89276709 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0260 |
2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1185-8064G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276709 | |||||||
| chr11:89276717 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1185-8056T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276717 | |||||||
| chr11:89276886 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02922.hp2 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-7887G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276886 | |||||||
| chr11:89276957 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
12 | HG00741.hp2 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-7816A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89276957 | |||||||
| chr11:89277032 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0070 others(29): Show |
32 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1185-7741G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277032 | |||||||
| chr11:89277059 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0062 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185-7714T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277059 | |||||||
| chr11:89277263 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1185-7510T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277263 | |||||||
| chr11:89277322 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1185-7451A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277322 | |||||||
| chr11:89277330 | G | A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG02145.hp2 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1185-7443G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277330 | |||||||
| chr11:89277441 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1185-7332T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277441 | |||||||
| chr11:89277459 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1185-7314A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277459 | |||||||
| chr11:89277500 | C | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0067 others(49): Show |
53 | HG00621.hp1 HG01243.hp2 HG01346.hp2 others(50): Show |
intron_variant | MODIFIER | c.1185-7273C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277500 | |||||||
| chr11:89277563 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1185-7210C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277563 | |||||||
| chr11:89277848 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0219 |
2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1185-6925C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277848 | |||||||
| chr11:89277878 | G | A | 11 | a0001c0001t0001g0166 a0003c0003t0001g0002 a0003c0003t0001g0003 others(8): Show |
13 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1185-6895G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89277878 | |||||||
| chr11:89278087 | A | G | 10 | a0001c0001t0001g0063 a0001c0001t0001g0119 a0001c0001t0001g0120 others(7): Show |
10 | HG01346.hp2 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1185-6686A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278087 | |||||||
| chr11:89278127 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0273 |
2 | NA18940.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1185-6646T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278127 | |||||||
| chr11:89278343 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0220 |
3 | HG01978.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1185-6430A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278343 | |||||||
| chr11:89278470 | G | T | 1 | a0001c0001t0001g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1185-6303G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278470 | |||||||
| chr11:89278504 | T | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(4): Show |
7 | HG01884.hp1 HG02615.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-6269T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278504 | |||||||
| chr11:89278565 | A | G | 2 | a0004c0005t0001g0175 a0004c0005t0001g0189 |
2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1185-6208A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278565 | |||||||
| chr11:89278647 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1185-6126C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278647 | |||||||
| chr11:89278653 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1185-6120G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278653 | |||||||
| chr11:89278767 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1185-6006C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278767 | |||||||
| chr11:89278819 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1185-5954G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278819 | |||||||
| chr11:89278894 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1185-5879T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278894 | |||||||
| chr11:89278917 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(44): Show |
48 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(45): Show |
intron_variant | MODIFIER | c.1185-5856C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89278917 | |||||||
| chr11:89279047 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0070 a0001c0001t0001g0073 others(5): Show |
8 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-5726A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89279047 | |||||||
| chr11:89279189 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0122 |
2 | HG01243.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1185-5584G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89279189 | |||||||
| chr11:89279230 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(38): Show |
42 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(39): Show |
intron_variant | MODIFIER | c.1185-5543C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89279230 | |||||||
| chr11:89279382 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1185-5391C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89279382 | |||||||
| chr11:89279522 | C | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0260 |
2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1185-5251C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89279522 | |||||||
| chr11:89279554 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-5219T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89279554 | |||||||
| chr11:89279711 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-5062T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89279711 | |||||||
| chr11:89280164 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-4609A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280164 | |||||||
| chr11:89280218 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0116 a0001c0001t0001g0166 others(32): Show |
37 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1185-4555G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280218 | |||||||
| chr11:89280295 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-4478A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280295 | |||||||
| chr11:89280529 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-4244C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280529 | |||||||
| chr11:89280629 | T | C | 68 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(65): Show |
69 | HG00621.hp1 HG01243.hp2 HG01346.hp2 others(66): Show |
intron_variant | MODIFIER | c.1185-4144T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280629 | |||||||
| chr11:89280708 | T | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-4065T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280708 | |||||||
| chr11:89280818 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-3955T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280818 | |||||||
| chr11:89280936 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-3837C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280936 | |||||||
| chr11:89280981 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-3792A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89280981 | |||||||
| chr11:89281066 | A | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0004t0001g0283 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-3707A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281066 | |||||||
| chr11:89281096 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1185-3677G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281096 | |||||||
| chr11:89281187 | T | C | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(139): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1185-3586T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281187 | |||||||
| chr11:89281349 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1185-3424G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281349 | |||||||
| chr11:89281414 | C | A | 1 | a0003c0003t0001g0022 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1185-3359C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281414 | |||||||
| chr11:89281529 | C | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02886.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-3244C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281529 | |||||||
| chr11:89281577 | C | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0004t0001g0283 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185-3196C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281577 | |||||||
| chr11:89281603 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-3170A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281603 | |||||||
| chr11:89281613 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1185-3160G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281613 | |||||||
| chr11:89281807 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-2966C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281807 | |||||||
| chr11:89281918 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1185-2855C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281918 | |||||||
| chr11:89281935 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1185-2838C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281935 | |||||||
| chr11:89281945 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1185-2828C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89281945 | |||||||
| chr11:89282029 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1185-2744T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282029 | |||||||
| chr11:89282136 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-2637T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282136 | |||||||
| chr11:89282156 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1185-2617C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282156 | |||||||
| chr11:89282487 | A | C | 1 | a0003c0003t0001g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1185-2286A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282487 | |||||||
| chr11:89282611 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1185-2162A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282611 | |||||||
| chr11:89282630 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-2143G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282630 | |||||||
| chr11:89282871 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1185-1902A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282871 | |||||||
| chr11:89282882 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1185-1891G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282882 | |||||||
| chr11:89282997 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-1776A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89282997 | |||||||
| chr11:89283405 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1185-1368T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89283405 | |||||||
| chr11:89283452 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1185-1321C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89283452 | |||||||
| chr11:89283457 | C | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0116 a0001c0001t0001g0166 others(32): Show |
37 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1185-1316C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89283457 | |||||||
| chr11:89283494 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-1279G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89283494 | |||||||
| chr11:89283510 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-1263G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89283510 | |||||||
| chr11:89283982 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-791G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89283982 | |||||||
| chr11:89284001 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1185-772T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89284001 | |||||||
| chr11:89284029 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1185-744G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89284029 | |||||||
| chr11:89284034 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1185-739C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89284034 | |||||||
| chr11:89284203 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1185-570G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89284203 | |||||||
| chr11:89284351 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1185-422C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89284351 | |||||||
| chr11:89284520 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1185-253G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 3/4 | chr11 | 89284520 | |||||||
| chr11:89285103 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1366+149A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285103 | |||||||
| chr11:89285113 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1366+159G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285113 | |||||||
| chr11:89285132 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1366+178T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285132 | |||||||
| chr11:89285272 | A | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(139): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1366+318A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285272 | |||||||
| chr11:89285290 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
8 | HG00639.hp1 HG00642.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+336T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285290 | |||||||
| chr11:89285405 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1366+451C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285405 | |||||||
| chr11:89285543 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+589T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285543 | |||||||
| chr11:89285617 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0260 |
2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1366+663T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285617 | |||||||
| chr11:89285678 | A | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG00558.hp1 NA18992.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+724A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285678 | |||||||
| chr11:89285829 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1366+875A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89285829 | |||||||
| chr11:89286011 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 |
3 | HG02615.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366+1057A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89286011 | |||||||
| chr11:89286166 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1366+1212G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89286166 | |||||||
| chr11:89286206 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(7): Show |
10 | HG01346.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1366+1252A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89286206 | |||||||
| chr11:89286551 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(40): Show |
44 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(41): Show |
intron_variant | MODIFIER | c.1366+1597C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89286551 | |||||||
| chr11:89286569 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1366+1615C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89286569 | |||||||
| chr11:89286635 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1366+1681G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89286635 | |||||||
| chr11:89286984 | A | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1366+2030A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89286984 | |||||||
| chr11:89287103 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1366+2149C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287103 | |||||||
| chr11:89287317 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1366+2363C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287317 | |||||||
| chr11:89287330 | T | C | 43 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(40): Show |
44 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(41): Show |
intron_variant | MODIFIER | c.1366+2376T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287330 | |||||||
| chr11:89287353 | A | G | 8 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+2399A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287353 | |||||||
| chr11:89287422 | T | C | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(138): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1366+2468T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287422 | |||||||
| chr11:89287588 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1366+2634T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287588 | |||||||
| chr11:89287602 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1366+2648C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287602 | |||||||
| chr11:89287647 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0193 a0001c0001t0001g0194 others(6): Show |
9 | HG01981.hp2 NA18941.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366+2693G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287647 | |||||||
| chr11:89287897 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1366+2943T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287897 | |||||||
| chr11:89287938 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1366+2984T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89287938 | |||||||
| chr11:89288103 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1366+3149C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288103 | |||||||
| chr11:89288129 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1366+3175T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288129 | |||||||
| chr11:89288166 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1366+3212C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288166 | |||||||
| chr11:89288244 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1366+3290T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288244 | |||||||
| chr11:89288375 | G | T | 1 | a0001c0001t0001g0258 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1366+3421G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288375 | |||||||
| chr11:89288406 | G | A | 61 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(58): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1366+3452G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288406 | |||||||
| chr11:89288523 | A | G | 12 | a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0001g0122 others(9): Show |
12 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366+3569A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288523 | |||||||
| chr11:89288568 | C | T | 12 | a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0001g0122 others(9): Show |
12 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366+3614C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288568 | |||||||
| chr11:89288596 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1366+3642C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288596 | |||||||
| chr11:89288614 | G | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG02622.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366+3660G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288614 | |||||||
| chr11:89288780 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1366+3826T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288780 | |||||||
| chr11:89288815 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1366+3861G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288815 | |||||||
| chr11:89288879 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1366+3925T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288879 | |||||||
| chr11:89288887 | AATT | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG02622.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366+3937_1366+393 others(7): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89288887 | ||||||
| chr11:89288902 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1366+3948C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288902 | |||||||
| chr11:89288948 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1366+3994C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89288948 | |||||||
| chr11:89289210 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1366+4256A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289210 | |||||||
| chr11:89289259 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1366+4305T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289259 | |||||||
| chr11:89289278 | G | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(40): Show |
46 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1366+4324G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289278 | |||||||
| chr11:89289346 | G | T | 1 | a0001c0001t0001g0015 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1366+4392G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289346 | |||||||
| chr11:89289505 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1366+4551G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289505 | |||||||
| chr11:89289511 | C | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(138): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1366+4557C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289511 | |||||||
| chr11:89289539 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 |
3 | HG02615.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366+4585G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289539 | |||||||
| chr11:89289547 | T | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG02922.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1366+4593T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289547 | |||||||
| chr11:89289892 | T | C | 43 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(40): Show |
44 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(41): Show |
intron_variant | MODIFIER | c.1366+4938T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289892 | |||||||
| chr11:89289977 | T | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0070 a0001c0001t0001g0073 others(5): Show |
8 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1366+5023T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289977 | |||||||
| chr11:89289995 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1366+5041T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89289995 | |||||||
| chr11:89290066 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1367-5077A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290066 | |||||||
| chr11:89290119 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1367-5024T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290119 | |||||||
| chr11:89290177 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1367-4966G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290177 | |||||||
| chr11:89290275 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1367-4868T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290275 | |||||||
| chr11:89290365 | G | A | 28 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0096 others(25): Show |
28 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1367-4778G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290365 | |||||||
| chr11:89290399 | T | A | 8 | a0001c0001t0001g0063 a0001c0001t0001g0070 a0001c0001t0001g0073 others(5): Show |
8 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-4744T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290399 | |||||||
| chr11:89290405 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1367-4738A>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290405 | |||||||
| chr11:89290508 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1367-4635A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290508 | |||||||
| chr11:89290528 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1367-4615T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290528 | |||||||
| chr11:89290557 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1367-4586A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290557 | |||||||
| chr11:89290672 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0116 a0001c0001t0001g0166 others(32): Show |
37 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1367-4471G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290672 | |||||||
| chr11:89290709 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1367-4434T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290709 | |||||||
| chr11:89290724 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(40): Show |
44 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(41): Show |
intron_variant | MODIFIER | c.1367-4419C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290724 | |||||||
| chr11:89290763 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 |
3 | HG02615.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1367-4380C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290763 | |||||||
| chr11:89290781 | C | A | 1 | a0003c0003t0001g0020 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1367-4362C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89290781 | |||||||
| chr11:89291021 | A | T | 8 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0004t0001g0283 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-4122A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291021 | |||||||
| chr11:89291153 | A | ACATATCT others(2): Show |
62 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(59): Show |
66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1367-3989_1367-398 others(13): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89291153 | ||||||
| chr11:89291183 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1367-3960G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291183 | |||||||
| chr11:89291233 | C | G | 8 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0004t0001g0283 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-3910C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291233 | |||||||
| chr11:89291287 | A | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(58): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1367-3856A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291287 | |||||||
| chr11:89291318 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1367-3825T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291318 | |||||||
| chr11:89291347 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1367-3796T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291347 | |||||||
| chr11:89291357 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1367-3786G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291357 | |||||||
| chr11:89291358 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18971.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1367-3785T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291358 | |||||||
| chr11:89291449 | C | T | 6 | a0001c0004t0001g0283 a0001c0004t0001g0284 a0001c0004t0001g0285 others(3): Show |
6 | HG02451.hp2 HG02886.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367-3694C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291449 | |||||||
| chr11:89291461 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1367-3682T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291461 | |||||||
| chr11:89291486 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1367-3657T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291486 | |||||||
| chr11:89291690 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1367-3453T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291690 | |||||||
| chr11:89291902 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1367-3241G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291902 | |||||||
| chr11:89291956 | C | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1367-3187C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89291956 | |||||||
| chr11:89292014 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1367-3129C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292014 | |||||||
| chr11:89292064 | A | G | 1 | a0005c0007t0001g0048 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1367-3079A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292064 | |||||||
| chr11:89292094 | C | T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0001g0122 others(6): Show |
9 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367-3049C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292094 | |||||||
| chr11:89292125 | A | G | 8 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0157 others(5): Show |
8 | HG01081.hp2 NA18944.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-3018A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292125 | |||||||
| chr11:89292126 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1367-3017T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292126 | |||||||
| chr11:89292550 | G | A | 8 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0004t0001g0283 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-2593G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292550 | |||||||
| chr11:89292670 | T | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(48): Show |
52 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(49): Show |
intron_variant | MODIFIER | c.1367-2473T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292670 | |||||||
| chr11:89292701 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1367-2442G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292701 | |||||||
| chr11:89292898 | C | G | 8 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367-2245C>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292898 | |||||||
| chr11:89292966 | CTT | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0004t0001g0283 others(5): Show |
8 | HG01243.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-2176_1367-217 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89292966 | |||||||
| chr11:89293178 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0076 |
2 | HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1367-1965T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293178 | |||||||
| chr11:89293239 | T | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(138): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1367-1904T>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293239 | |||||||
| chr11:89293286 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1367-1857T>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293286 | |||||||
| chr11:89293336 | T | TAC | 18 | a0001c0001t0001g0045 a0001c0001t0001g0101 a0001c0001t0001g0128 others(15): Show |
19 | HG00423.hp1 HG00639.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1367-1773_1367-177 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89293336 | ||||||
| chr11:89293336 | TAC | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(93): Show |
99 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1367-1773_1367-177 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89293336 | ||||||
| chr11:89293336 | TACAC | T | 47 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0051 others(44): Show |
47 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1367-1775_1367-177 others(8): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89293336 | ||||||
| chr11:89293336 | TACACAC | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(63): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1367-1777_1367-177 others(10): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89293336 | ||||||
| chr11:89293336 | TACACACA others(1): Show |
T | 9 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(6): Show |
9 | HG01074.hp2 HG01099.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367-1779_1367-177 others(12): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89293336 | ||||||
| chr11:89293354 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367-1789C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293354 | |||||||
| chr11:89293412 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1367-1731G>C | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293412 | |||||||
| chr11:89293436 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1367-1707G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293436 | |||||||
| chr11:89293449 | G | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(49): Show |
53 | HG00621.hp1 HG01346.hp2 HG01884.hp2 others(50): Show |
intron_variant | MODIFIER | c.1367-1694G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293449 | |||||||
| chr11:89293648 | A | AT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0116 others(36): Show |
41 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1367-1494dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89293648 | ||||||
| chr11:89293832 | G | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0108 |
2 | NA18992.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1367-1311G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89293832 | |||||||
| chr11:89294014 | T | G | 1 | a0001c0001t0001g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1367-1129T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294014 | |||||||
| chr11:89294028 | A | AT | 8 | a0001c0001t0001g0063 a0001c0001t0001g0070 a0001c0001t0001g0073 others(5): Show |
8 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-1106dupT | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89294028 | ||||||
| chr11:89294028 | A | ATT | 43 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0038 others(40): Show |
44 | HG00621.hp1 HG01884.hp2 HG01978.hp2 others(41): Show |
intron_variant | MODIFIER | c.1367-1107_1367-110 others(6): Show |
TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 89294028 | ||||||
| chr11:89294128 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1367-1015C>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294128 | |||||||
| chr11:89294204 | G | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG02622.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367-939G>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294204 | |||||||
| chr11:89294633 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1367-510A>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294633 | |||||||
| chr11:89294664 | A | T | 1 | a0003c0003t0001g0018 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1367-479A>T | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294664 | |||||||
| chr11:89294875 | T | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(71): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1367-268T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294875 | |||||||
| chr11:89294896 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1367-247C>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294896 | |||||||
| chr11:89294981 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1367-162G>A | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89294981 | |||||||
| chr11:89295000 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1367-143T>G | TYR | ENSG00000077498.9 | transcript | ENST00000263321.6 | protein_coding | 4/4 | chr11 | 89295000 |