Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7982 |
| ensemblid | ENSG00000004866.22 |
| hgncid | 11351 |
| symbol | ST7 |
| name | suppression of tumorigenicity 7 |
| refseq_nuc | NM_001369598.1 |
| refseq_prot | NP_001356527.1 |
| ensembl_nuc | ENST00000323984.8 |
| ensembl_prot | ENSP00000325673.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 116953501 |
| end | 117230176 |
| strand | + |
| ver | v1.2 |
| region | chr7:116953501-117230176 |
| region5000 | chr7:116948501-117235176 |
| regionname0 | ST7_chr7_116953501_117230176 |
| regionname5000 | ST7_chr7_116948501_117235176 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1731 | 187 | 69 | 36 | 58 | 10 | 12 | ST7_chr7_116948501_117235176 | ST7 | ATGGC others(1726): Show |
chr7 | 116948501 | 117235176 | ||
| a0001c0002 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | ATGGC others(1726): Show |
chr7 | 116948501 | 117235176 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2093 | 187 | 69 | 36 | 58 | 10 | 12 | ST7_chr7_116948501_117235176 | ST7 | AGACA others(2088): Show |
chr7 | 116948501 | 117235176 |
| a0001c0002t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | AGACA others(2088): Show |
chr7 | 116948501 | 117235176 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0119 | REF | REF | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0060 | REF | REF | ST7_chr7_116948501_117235176 | ST7 | chr7 | 116948501 | 117235176 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117099823 | A | G | 1 | a0001c0002 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.213A>G | p.Ser71Ser | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/16 | 253/2093 | 213/1734 | 71/577 | chr7 | 117099823 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116953749 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 |
3 | HG02717.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+58T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116953749 | |||||||
| chr7:116953758 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.151+67C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116953758 | |||||||
| chr7:116953887 | G | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(38): Show |
41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+196G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116953887 | |||||||
| chr7:116954326 | G | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+635G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116954326 | |||||||
| chr7:116954344 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+653T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116954344 | |||||||
| chr7:116954699 | GTTTTAAA | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01943.hp1 HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.151+1015_151+1021d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116954699 | ||||||
| chr7:116954768 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.151+1077A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116954768 | |||||||
| chr7:116955076 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG02040.hp2 HG02273.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+1385G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116955076 | |||||||
| chr7:116955383 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+1692C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116955383 | |||||||
| chr7:116956643 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+2952A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956643 | |||||||
| chr7:116956751 | T | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3060T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956751 | |||||||
| chr7:116956758 | G | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02486.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.151+3067G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956758 | |||||||
| chr7:116956825 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151+3134T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956825 | |||||||
| chr7:116956857 | C | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0148 others(39): Show |
42 | HG00323.hp1 HG00438.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.151+3166C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116956857 | |||||||
| chr7:116957069 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+3378C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957069 | |||||||
| chr7:116957087 | C | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(14): Show |
17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+3396C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957087 | |||||||
| chr7:116957175 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3484C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957175 | |||||||
| chr7:116957369 | T | G | 15 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(12): Show |
15 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.151+3678T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957369 | |||||||
| chr7:116957644 | A | G | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+3953A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116957644 | |||||||
| chr7:116958021 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
10 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+4330C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958021 | |||||||
| chr7:116958162 | A | AT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.151+4495dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116958162 | ||||||
| chr7:116958162 | A | ATT | 19 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0043 others(16): Show |
19 | HG00673.hp2 HG01358.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+4494_151+4495d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116958162 | ||||||
| chr7:116958670 | C | T | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+4979C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958670 | |||||||
| chr7:116958681 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.151+4990A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958681 | |||||||
| chr7:116958730 | A | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+5039A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958730 | |||||||
| chr7:116958789 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.151+5098T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116958789 | |||||||
| chr7:116959010 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.151+5319A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959010 | |||||||
| chr7:116959089 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+5398C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959089 | |||||||
| chr7:116959097 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+5406C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959097 | |||||||
| chr7:116959359 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.151+5668T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959359 | |||||||
| chr7:116959995 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+6304A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116959995 | |||||||
| chr7:116960169 | G | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+6478G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960169 | |||||||
| chr7:116960184 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.151+6493T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960184 | |||||||
| chr7:116960309 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.151+6618C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960309 | |||||||
| chr7:116960490 | A | C | 1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.151+6799A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960490 | |||||||
| chr7:116960509 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+6818C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116960509 | |||||||
| chr7:116961256 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.151+7565C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961256 | |||||||
| chr7:116961395 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0187 |
3 | NA19000.hp1 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.151+7704A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961395 | |||||||
| chr7:116961428 | T | C | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+7737T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961428 | |||||||
| chr7:116961555 | C | CGT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0022 others(12): Show |
15 | HG00408.hp1 HG01192.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+7902_151+7903d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(20): Show |
23 | HG00673.hp1 HG00673.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.151+7900_151+7903d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGTGT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(7): Show |
10 | HG00642.hp1 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+7898_151+7903d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGTGTG others(1): Show |
6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG00408.hp2 HG01358.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+7896_151+7903d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGTGTG others(3): Show |
4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG00438.hp2 HG02040.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+7894_151+7903d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGTGTG others(5): Show |
3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG00738.hp2 NA18951.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.151+7892_151+7903d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGTGTG others(7): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG02717.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.151+7890_151+7903d others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.151+7888_151+7903d others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | C | CGTGTGTG others(11): Show |
1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.151+7886_151+7903d others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | CGT | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0043 others(67): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.151+7902_151+7903d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | CGTGT | C | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0090 others(4): Show |
7 | HG00738.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+7900_151+7903d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | CGTGTGT | C | 7 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02451.hp1 HG02647.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+7898_151+7903d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961555 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+7894_151+7903d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116961555 | ||||||
| chr7:116961767 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+8076T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961767 | |||||||
| chr7:116961785 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.151+8094A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961785 | |||||||
| chr7:116961810 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+8119A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116961810 | |||||||
| chr7:116962139 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+8448G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116962139 | |||||||
| chr7:116962397 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.151+8706C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116962397 | |||||||
| chr7:116962416 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.151+8725C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116962416 | |||||||
| chr7:116963411 | A | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+9720A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963411 | |||||||
| chr7:116963632 | C | CT | 6 | a0001c0001t0001g0062 a0001c0001t0001g0112 a0001c0001t0001g0120 others(3): Show |
6 | HG02717.hp2 HG03209.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+9957dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116963632 | ||||||
| chr7:116963632 | CT | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+9957delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116963632 | ||||||
| chr7:116963654 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+9963C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963654 | |||||||
| chr7:116963891 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+10200A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963891 | |||||||
| chr7:116963950 | A | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+10259A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116963950 | |||||||
| chr7:116964131 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+10440C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964131 | |||||||
| chr7:116964140 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+10449T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964140 | |||||||
| chr7:116964322 | T | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+10631T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964322 | |||||||
| chr7:116964716 | A | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+11025A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116964716 | |||||||
| chr7:116965339 | C | CA | 42 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(39): Show |
42 | HG00408.hp1 HG00673.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.151+11669dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965339 | ||||||
| chr7:116965339 | C | CAA | 8 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0061 others(5): Show |
8 | HG01433.hp2 HG02109.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+11668_151+1166 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965339 | ||||||
| chr7:116965339 | CA | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG02040.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+11669delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965339 | ||||||
| chr7:116965481 | C | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+11790C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116965481 | |||||||
| chr7:116965565 | C | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+11874C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116965565 | |||||||
| chr7:116965763 | G | GAAAAAGA others(321): Show |
1 | a0001c0001t0001g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.151+12085_151+1208 others(332): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965763 | ||||||
| chr7:116965763 | G | GAAAAAGA others(327): Show |
1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.151+12085_151+1208 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116965763 | ||||||
| chr7:116966037 | A | ATACCCAA others(6): Show |
1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.151+12348_151+1236 others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966037 | ||||||
| chr7:116966187 | C | T | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+12496C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966187 | |||||||
| chr7:116966232 | TTTTCTTT others(4): Show |
T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.151+12552_151+1256 others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966232 | ||||||
| chr7:116966247 | C | CT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG00323.hp2 HG00642.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+12576dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966247 | ||||||
| chr7:116966247 | CT | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0058 a0001c0001t0001g0059 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+12576delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116966247 | ||||||
| chr7:116966251 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0102 |
2 | HG01978.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.151+12560T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966251 | |||||||
| chr7:116966385 | G | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+12694G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966385 | |||||||
| chr7:116966542 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+12851C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966542 | |||||||
| chr7:116966742 | T | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+13051T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966742 | |||||||
| chr7:116966762 | C | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+13071C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966762 | |||||||
| chr7:116966782 | C | A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+13091C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966782 | |||||||
| chr7:116966782 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.151+13091C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966782 | |||||||
| chr7:116966783 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.151+13092A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116966783 | |||||||
| chr7:116967118 | C | CT | 6 | a0001c0001t0001g0062 a0001c0001t0001g0133 a0001c0001t0001g0134 others(3): Show |
6 | HG00438.hp2 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+13442dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116967118 | ||||||
| chr7:116967118 | C | CTT | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(8): Show |
11 | HG00408.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+13441_151+1344 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116967118 | ||||||
| chr7:116967118 | CT | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0064 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.151+13442delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116967118 | ||||||
| chr7:116967181 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151+13490T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967181 | |||||||
| chr7:116967293 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+13602G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967293 | |||||||
| chr7:116967447 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.151+13756T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967447 | |||||||
| chr7:116967488 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+13797C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967488 | |||||||
| chr7:116967559 | T | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+13868T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967559 | |||||||
| chr7:116967560 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151+13869A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116967560 | |||||||
| chr7:116968127 | A | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+14436A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968127 | |||||||
| chr7:116968256 | TCTCC | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0086 a0001c0001t0001g0087 others(6): Show |
9 | HG01433.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+14602_151+1460 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968256 | ||||||
| chr7:116968256 | TCTCCCTC others(1): Show |
T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0097 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.151+14598_151+1460 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968256 | ||||||
| chr7:116968256 | TCTCCCTC others(5): Show |
T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.151+14594_151+1460 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968256 | ||||||
| chr7:116968260 | C | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.151+14569C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968260 | |||||||
| chr7:116968269 | CTCCCTCC others(29): Show |
C | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+14582_151+1461 others(40): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968269 | ||||||
| chr7:116968279 | C | CCCTCCTT others(21): Show |
12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14593_151+1459 others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968279 | ||||||
| chr7:116968281 | CTCCCTCC others(17): Show |
C | 17 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0064 others(14): Show |
17 | HG00738.hp1 HG01081.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+14594_151+1461 others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968281 | ||||||
| chr7:116968285 | C | T | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+14594C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968285 | |||||||
| chr7:116968285 | CTCCCTCC others(5): Show |
C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+14598_151+1460 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968285 | ||||||
| chr7:116968285 | CTCCCTCC others(13): Show |
C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.151+14598_151+1461 others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968285 | ||||||
| chr7:116968285 | CTCCCTCC others(17): Show |
C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+14598_151+1462 others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968285 | ||||||
| chr7:116968289 | C | T | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+14598C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968289 | |||||||
| chr7:116968289 | CTCCCTCC others(9): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0133 |
3 | HG02257.hp2 HG02523.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.151+14602_151+1461 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116968289 | ||||||
| chr7:116968293 | C | T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+14602C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968293 | |||||||
| chr7:116968297 | T | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14606T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968297 | |||||||
| chr7:116968301 | T | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14610T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968301 | |||||||
| chr7:116968305 | T | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+14614T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968305 | |||||||
| chr7:116968417 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.151+14726G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968417 | |||||||
| chr7:116968446 | A | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+14755A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968446 | |||||||
| chr7:116968447 | A | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+14756A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968447 | |||||||
| chr7:116968566 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.151+14875G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968566 | |||||||
| chr7:116968580 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.151+14889G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968580 | |||||||
| chr7:116968825 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+15134A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968825 | |||||||
| chr7:116968975 | T | C | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+15284T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116968975 | |||||||
| chr7:116969309 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+15618T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969309 | |||||||
| chr7:116969481 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.151+15790T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969481 | |||||||
| chr7:116969740 | A | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+16049A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969740 | |||||||
| chr7:116969781 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+16090A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116969781 | |||||||
| chr7:116970168 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.151+16477G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970168 | |||||||
| chr7:116970183 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(37): Show |
40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.151+16492A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970183 | |||||||
| chr7:116970445 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151+16754G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970445 | |||||||
| chr7:116970510 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+16819C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970510 | |||||||
| chr7:116970664 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.151+16973A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116970664 | |||||||
| chr7:116971092 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.151+17401T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971092 | |||||||
| chr7:116971515 | G | GA | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+17834dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116971515 | ||||||
| chr7:116971555 | G | GTA | 2 | a0001c0001t0001g0116 a0001c0001t0001g0123 |
2 | HG01358.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.151+17868_151+1786 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116971555 | ||||||
| chr7:116971724 | G | A | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0131 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+18033G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971724 | |||||||
| chr7:116971784 | CAAAAGTG others(3): Show |
C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+18097_151+1810 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116971784 | ||||||
| chr7:116971795 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.151+18104A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971795 | |||||||
| chr7:116971921 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.151+18230C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116971921 | |||||||
| chr7:116972034 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+18343C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116972034 | |||||||
| chr7:116972316 | C | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(14): Show |
17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+18625C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116972316 | |||||||
| chr7:116972673 | G | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+18982G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116972673 | |||||||
| chr7:116973113 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+19422C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973113 | |||||||
| chr7:116973132 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+19441C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973132 | |||||||
| chr7:116973520 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.151+19829G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973520 | |||||||
| chr7:116973813 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+20122T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116973813 | |||||||
| chr7:116974059 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+20368A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974059 | |||||||
| chr7:116974512 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+20821C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974512 | |||||||
| chr7:116974542 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+20851C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974542 | |||||||
| chr7:116974543 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+20852G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974543 | |||||||
| chr7:116974736 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151+21045C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974736 | |||||||
| chr7:116974907 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+21216T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116974907 | |||||||
| chr7:116975065 | C | T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+21374C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975065 | |||||||
| chr7:116975142 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+21451T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975142 | |||||||
| chr7:116975179 | A | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+21488A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975179 | |||||||
| chr7:116975414 | A | AT | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+21734dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116975414 | ||||||
| chr7:116975438 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+21747C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975438 | |||||||
| chr7:116975510 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+21819C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975510 | |||||||
| chr7:116975985 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(38): Show |
41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+22294G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116975985 | |||||||
| chr7:116976137 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.151+22446A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976137 | |||||||
| chr7:116976145 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+22454A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976145 | |||||||
| chr7:116976644 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.151+22953A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976644 | |||||||
| chr7:116976659 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.151+22968C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976659 | |||||||
| chr7:116976775 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.151+23084C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976775 | |||||||
| chr7:116976782 | G | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+23091G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976782 | |||||||
| chr7:116976783 | TACCATTA others(11): Show |
T | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.151+23094_151+2311 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116976783 | ||||||
| chr7:116976795 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.151+23104C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116976795 | |||||||
| chr7:116976847 | GATGTTAC others(3): Show |
G | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.151+23158_151+2316 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116976847 | ||||||
| chr7:116977226 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.151+23535A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977226 | |||||||
| chr7:116977447 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151+23756G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977447 | |||||||
| chr7:116977478 | G | A | 13 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
13 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+23787G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977478 | |||||||
| chr7:116977630 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.151+23939C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977630 | |||||||
| chr7:116977761 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+24070T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977761 | |||||||
| chr7:116977849 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0148 others(14): Show |
17 | HG01255.hp1 HG02004.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.151+24158G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977849 | |||||||
| chr7:116977896 | A | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0122 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.151+24205A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116977896 | |||||||
| chr7:116978172 | A | T | 1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.151+24481A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116978172 | |||||||
| chr7:116978568 | T | TTCTA | 10 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+24898_151+2490 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116978568 | ||||||
| chr7:116979094 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.151+25403G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979094 | |||||||
| chr7:116979161 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.151+25470A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979161 | |||||||
| chr7:116979196 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0104 |
2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.151+25505T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979196 | |||||||
| chr7:116979222 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151+25531G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979222 | |||||||
| chr7:116979328 | CAA | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.151+25638_151+2563 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979328 | |||||||
| chr7:116979549 | A | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+25858A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979549 | |||||||
| chr7:116979564 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.151+25873T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979564 | |||||||
| chr7:116979720 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+26029C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979720 | |||||||
| chr7:116979868 | C | T | 16 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(13): Show |
16 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.151+26177C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979868 | |||||||
| chr7:116979951 | T | G | 5 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0105 others(2): Show |
5 | HG00099.hp1 HG00741.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+26260T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979951 | |||||||
| chr7:116979958 | C | CT | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+26284dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | ||||||
| chr7:116979958 | C | CTTTTTTT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0061 others(4): Show |
7 | HG01433.hp2 HG02280.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+26278_151+2628 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | ||||||
| chr7:116979958 | C | CTTTTTTT others(2): Show |
12 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0039 others(9): Show |
12 | HG00280.hp2 HG01496.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+26276_151+2628 others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | ||||||
| chr7:116979958 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(1): Show |
4 | HG01358.hp2 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+26275_151+2628 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | ||||||
| chr7:116979958 | CTTTTTT | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+26279_151+2628 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116979958 | ||||||
| chr7:116979982 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0178 |
2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151+26291A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116979982 | |||||||
| chr7:116980049 | C | G | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+26358C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980049 | |||||||
| chr7:116980169 | G | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+26478G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980169 | |||||||
| chr7:116980752 | C | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0178 |
2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151+27061C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980752 | |||||||
| chr7:116980753 | A | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0177 |
3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.151+27062A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980753 | |||||||
| chr7:116980843 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.151+27152A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980843 | |||||||
| chr7:116980847 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+27156G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116980847 | |||||||
| chr7:116981076 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+27385G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981076 | |||||||
| chr7:116981222 | C | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+27531C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981222 | |||||||
| chr7:116981497 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.151+27806A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981497 | |||||||
| chr7:116981806 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+28115A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116981806 | |||||||
| chr7:116982243 | A | T | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+28552A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982243 | |||||||
| chr7:116982310 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.151+28619C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982310 | |||||||
| chr7:116982398 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0122 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.151+28707A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982398 | |||||||
| chr7:116982494 | T | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+28803T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982494 | |||||||
| chr7:116982730 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+29039C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982730 | |||||||
| chr7:116982812 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151+29121G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982812 | |||||||
| chr7:116982903 | A | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.151+29212A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982903 | |||||||
| chr7:116982984 | C | T | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+29293C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116982984 | |||||||
| chr7:116983249 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151+29558G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116983249 | |||||||
| chr7:116983680 | G | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+29989G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116983680 | |||||||
| chr7:116983779 | G | A | 10 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0108 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+30088G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116983779 | |||||||
| chr7:116984010 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.151+30319A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984010 | |||||||
| chr7:116984113 | C | CTG | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.151+30452_151+3045 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | ||||||
| chr7:116984113 | C | CTGTG | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0031 others(10): Show |
13 | HG01192.hp2 HG01978.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+30450_151+3045 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | ||||||
| chr7:116984113 | C | CTGTGTG | 16 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0086 others(13): Show |
16 | HG00323.hp1 HG00438.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.151+30448_151+3045 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | ||||||
| chr7:116984113 | C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0184 |
3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.151+30446_151+3045 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | ||||||
| chr7:116984113 | CTG | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0148 |
2 | NA19030.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.151+30452_151+3045 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | ||||||
| chr7:116984113 | CTGTG | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.151+30450_151+3045 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984113 | ||||||
| chr7:116984143 | GTC | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+30454_151+3045 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116984143 | ||||||
| chr7:116984145 | C | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+30454C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984145 | |||||||
| chr7:116984147 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+30456A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984147 | |||||||
| chr7:116984365 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+30674T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984365 | |||||||
| chr7:116984973 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.151+31282A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116984973 | |||||||
| chr7:116985032 | A | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+31341A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985032 | |||||||
| chr7:116985061 | A | G | 11 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(8): Show |
11 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.151+31370A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985061 | |||||||
| chr7:116985178 | A | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(14): Show |
17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+31487A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985178 | |||||||
| chr7:116985531 | AT | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+31845delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116985531 | ||||||
| chr7:116985793 | T | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+32102T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985793 | |||||||
| chr7:116985956 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+32265G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116985956 | |||||||
| chr7:116986102 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+32411G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986102 | |||||||
| chr7:116986204 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0159 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.151+32513T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986204 | |||||||
| chr7:116986206 | G | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+32515G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986206 | |||||||
| chr7:116986321 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.151+32630A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116986321 | |||||||
| chr7:116987031 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0027 |
2 | HG01934.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.151+33340C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116987031 | |||||||
| chr7:116988364 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+34673G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116988364 | |||||||
| chr7:116988656 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.151+34965G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116988656 | |||||||
| chr7:116989332 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+35641G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989332 | |||||||
| chr7:116989514 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+35823T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989514 | |||||||
| chr7:116989681 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.151+35990A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989681 | |||||||
| chr7:116989682 | T | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0148 others(28): Show |
31 | HG00323.hp1 HG00438.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.151+35991T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116989682 | |||||||
| chr7:116990323 | C | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+36632C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116990323 | |||||||
| chr7:116990422 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+36731G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116990422 | |||||||
| chr7:116990959 | C | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+37268C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116990959 | |||||||
| chr7:116991059 | G | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0100 a0001c0001t0001g0102 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.151+37368G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991059 | |||||||
| chr7:116991069 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+37378G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991069 | |||||||
| chr7:116991196 | C | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+37505C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991196 | |||||||
| chr7:116991233 | A | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+37542A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991233 | |||||||
| chr7:116991240 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+37549C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991240 | |||||||
| chr7:116991442 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151+37751T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991442 | |||||||
| chr7:116991483 | A | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+37792A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991483 | |||||||
| chr7:116991534 | C | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+37843C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991534 | |||||||
| chr7:116991550 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0177 |
3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.151+37859G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991550 | |||||||
| chr7:116991595 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(38): Show |
41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+37904C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991595 | |||||||
| chr7:116991655 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+37964A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116991655 | |||||||
| chr7:116992000 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+38309C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992000 | |||||||
| chr7:116992598 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+38907G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992598 | |||||||
| chr7:116992609 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+38918G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992609 | |||||||
| chr7:116992646 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.151+38955A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992646 | |||||||
| chr7:116992683 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.151+38992A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992683 | |||||||
| chr7:116992932 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.151+39241C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116992932 | |||||||
| chr7:116993307 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.151+39616G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993307 | |||||||
| chr7:116993322 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.151+39631T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993322 | |||||||
| chr7:116993466 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.151+39775G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993466 | |||||||
| chr7:116993644 | T | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+39953T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116993644 | |||||||
| chr7:116994019 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+40328T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994019 | |||||||
| chr7:116994053 | G | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+40362G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994053 | |||||||
| chr7:116994475 | G | T | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+40784G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994475 | |||||||
| chr7:116994680 | T | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+40989T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994680 | |||||||
| chr7:116994791 | C | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+41100C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994791 | |||||||
| chr7:116994812 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.151+41121A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994812 | |||||||
| chr7:116994836 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+41145G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994836 | |||||||
| chr7:116994929 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.151+41238C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994929 | |||||||
| chr7:116994994 | T | C | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+41303T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116994994 | |||||||
| chr7:116995145 | T | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+41454T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116995145 | |||||||
| chr7:116995651 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+41960C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116995651 | |||||||
| chr7:116995818 | C | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.151+42127C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116995818 | |||||||
| chr7:116996082 | G | GT | 46 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(43): Show |
46 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.151+42408dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116996082 | ||||||
| chr7:116996082 | G | GTTT | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+42406_151+4240 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116996082 | ||||||
| chr7:116996167 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+42476C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996167 | |||||||
| chr7:116996169 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+42478C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996169 | |||||||
| chr7:116996391 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.151+42700T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996391 | |||||||
| chr7:116996566 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.151+42875C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996566 | |||||||
| chr7:116996600 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151+42909C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996600 | |||||||
| chr7:116996655 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+42964A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996655 | |||||||
| chr7:116996911 | T | C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+43220T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996911 | |||||||
| chr7:116996976 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.151+43285G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116996976 | |||||||
| chr7:116997038 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+43347G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997038 | |||||||
| chr7:116997039 | T | C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0177 |
3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.151+43348T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997039 | |||||||
| chr7:116997246 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG00323.hp2 HG00642.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.151+43555G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997246 | |||||||
| chr7:116997268 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+43577C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997268 | |||||||
| chr7:116997338 | G | T | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+43647G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997338 | |||||||
| chr7:116997383 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+43692G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997383 | |||||||
| chr7:116997535 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(38): Show |
41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+43844T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997535 | |||||||
| chr7:116997635 | G | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(38): Show |
41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.151+43944G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997635 | |||||||
| chr7:116997695 | T | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+44004T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997695 | |||||||
| chr7:116997777 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151+44086C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997777 | |||||||
| chr7:116997945 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+44254C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997945 | |||||||
| chr7:116997987 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.151+44296G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997987 | |||||||
| chr7:116997997 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+44306G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116997997 | |||||||
| chr7:116998014 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.151+44323C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998014 | |||||||
| chr7:116998106 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+44415C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998106 | |||||||
| chr7:116998194 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | NA18974.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.151+44503G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998194 | |||||||
| chr7:116998238 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+44547G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998238 | |||||||
| chr7:116998251 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+44560C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998251 | |||||||
| chr7:116998273 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+44582G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998273 | |||||||
| chr7:116998304 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.151+44613C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998304 | |||||||
| chr7:116998373 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.151+44682C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998373 | |||||||
| chr7:116998502 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.151+44811C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998502 | |||||||
| chr7:116998655 | C | G | 13 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
13 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+44964C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998655 | |||||||
| chr7:116998699 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.151+45008C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116998699 | |||||||
| chr7:116999367 | G | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+45676G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999367 | |||||||
| chr7:116999370 | A | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+45679A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999370 | |||||||
| chr7:116999519 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0159 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.151+45828C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999519 | |||||||
| chr7:116999808 | C | CT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.151+46137dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116999808 | ||||||
| chr7:116999808 | C | CTT | 65 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(62): Show |
65 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.151+46136_151+4613 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116999808 | ||||||
| chr7:116999808 | C | CTTT | 10 | a0001c0001t0001g0102 a0001c0001t0001g0158 a0001c0001t0001g0160 others(7): Show |
10 | HG01192.hp1 HG01978.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+46135_151+4613 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 116999808 | ||||||
| chr7:116999813 | T | TC | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+46122_151+4612 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999813 | |||||||
| chr7:116999817 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+46126T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 116999817 | |||||||
| chr7:117000091 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.151+46400G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000091 | |||||||
| chr7:117000203 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.151+46512T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000203 | |||||||
| chr7:117000266 | G | C | 17 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(14): Show |
17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+46575G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000266 | |||||||
| chr7:117000487 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+46796G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000487 | |||||||
| chr7:117000628 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+46937G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000628 | |||||||
| chr7:117000836 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+47145C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117000836 | |||||||
| chr7:117001205 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.151+47514A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001205 | |||||||
| chr7:117001279 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151+47588A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001279 | |||||||
| chr7:117001331 | GA | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.151+47647delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117001331 | ||||||
| chr7:117001341 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+47650T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001341 | |||||||
| chr7:117001406 | C | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0187 |
2 | NA19000.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.151+47715C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001406 | |||||||
| chr7:117001474 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+47783G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001474 | |||||||
| chr7:117001494 | C | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 |
3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.151+47803C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117001494 | |||||||
| chr7:117002184 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+48493C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002184 | |||||||
| chr7:117002404 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+48713C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002404 | |||||||
| chr7:117002420 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.151+48729C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002420 | |||||||
| chr7:117002433 | A | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+48742A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117002433 | |||||||
| chr7:117002639 | C | CTG | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0081 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+48974_151+4897 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | ||||||
| chr7:117002639 | C | CTGTG | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.151+48972_151+4897 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | ||||||
| chr7:117002639 | C | CTGTGTG | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(93): Show |
96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.151+48970_151+4897 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | ||||||
| chr7:117002639 | C | CTGTGTGT others(1): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(9): Show |
12 | HG01192.hp1 HG02027.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+48968_151+4897 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | ||||||
| chr7:117002639 | CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+48960_151+4897 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002639 | ||||||
| chr7:117002813 | C | CT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): Show |
121 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.151+49148dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002813 | ||||||
| chr7:117002813 | C | CTT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(31): Show |
34 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.151+49147_151+4914 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002813 | ||||||
| chr7:117002813 | CTTTTTTT | C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+49142_151+4914 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117002813 | ||||||
| chr7:117003016 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+49325T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003016 | |||||||
| chr7:117003161 | T | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+49470T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003161 | |||||||
| chr7:117003189 | C | T | 14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
14 | HG00738.hp1 HG01081.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+49498C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003189 | |||||||
| chr7:117003656 | C | T | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+49965C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117003656 | |||||||
| chr7:117004096 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.151+50405G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004096 | |||||||
| chr7:117004296 | C | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+50605C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004296 | |||||||
| chr7:117004343 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+50652T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004343 | |||||||
| chr7:117004430 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.151+50739G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004430 | |||||||
| chr7:117004619 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.151+50928C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004619 | |||||||
| chr7:117004905 | T | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+51214T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117004905 | |||||||
| chr7:117005286 | T | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0089 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.151+51595T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005286 | |||||||
| chr7:117005325 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.151+51634T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005325 | |||||||
| chr7:117005420 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.151+51729T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005420 | |||||||
| chr7:117005572 | G | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+51881G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005572 | |||||||
| chr7:117005715 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.151+52024C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005715 | |||||||
| chr7:117005782 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151+52091C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005782 | |||||||
| chr7:117005825 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+52134A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005825 | |||||||
| chr7:117005826 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+52135T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117005826 | |||||||
| chr7:117006085 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.151+52394G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117006085 | |||||||
| chr7:117006473 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+52782C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117006473 | |||||||
| chr7:117006748 | A | G | 9 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
9 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+53057A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117006748 | |||||||
| chr7:117007890 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+54199C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117007890 | |||||||
| chr7:117008004 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG02040.hp2 HG02273.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+54313T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117008004 | |||||||
| chr7:117009012 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.151+55321T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009012 | |||||||
| chr7:117009253 | TTTTGTTT others(11): Show |
T | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+55566_151+5558 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117009253 | ||||||
| chr7:117009262 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+55571T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009262 | |||||||
| chr7:117009264 | T | G | 12 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(9): Show |
12 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+55573T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009264 | |||||||
| chr7:117009266 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.151+55575T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009266 | |||||||
| chr7:117009269 | TTG | T | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+55580_151+5558 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117009269 | ||||||
| chr7:117009270 | TG | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.151+55580delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009270 | |||||||
| chr7:117009271 | G | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01433.hp2 HG02071.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+55580G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009271 | |||||||
| chr7:117009784 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+56093G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117009784 | |||||||
| chr7:117010520 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+56829G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117010520 | |||||||
| chr7:117010790 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0187 |
3 | NA19000.hp1 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.151+57099T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117010790 | |||||||
| chr7:117010873 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.151+57182G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117010873 | |||||||
| chr7:117011134 | T | TTG | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0093 others(5): Show |
8 | HG01433.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+57461_151+5746 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117011134 | ||||||
| chr7:117011247 | C | G | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
6 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+57556C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011247 | |||||||
| chr7:117011278 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.151+57587C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011278 | |||||||
| chr7:117011355 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+57664C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011355 | |||||||
| chr7:117011761 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.151+58070C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011761 | |||||||
| chr7:117011762 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.151+58071T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011762 | |||||||
| chr7:117011778 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+58087C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011778 | |||||||
| chr7:117011908 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+58217A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117011908 | |||||||
| chr7:117012189 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.151+58498T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012189 | |||||||
| chr7:117012220 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 |
3 | NA18990.hp1 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.151+58529C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012220 | |||||||
| chr7:117012283 | A | AT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(36): Show |
39 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.151+58608dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117012283 | ||||||
| chr7:117012413 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+58722G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012413 | |||||||
| chr7:117012480 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0084 |
3 | NA18990.hp1 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.151+58789G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012480 | |||||||
| chr7:117012716 | T | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+59025T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117012716 | |||||||
| chr7:117013432 | T | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+59741T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013432 | |||||||
| chr7:117013510 | G | GTACTTTC | 2 | a0001c0001t0001g0113 a0001c0001t0001g0183 |
2 | HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.151+59821_151+5982 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117013510 | ||||||
| chr7:117013512 | A | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+59821A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013512 | |||||||
| chr7:117013782 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.151+60091G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013782 | |||||||
| chr7:117013801 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.151+60110C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117013801 | |||||||
| chr7:117013902 | CTAGAATT others(2): Show |
C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 |
3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.151+60223_151+6023 others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117013902 | ||||||
| chr7:117014147 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+60456A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117014147 | |||||||
| chr7:117014155 | G | T | 17 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(14): Show |
17 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.151+60464G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117014155 | |||||||
| chr7:117014287 | G | GATTGAAA others(2): Show |
181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+60600_151+6060 others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117014287 | ||||||
| chr7:117015804 | G | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+62113G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117015804 | |||||||
| chr7:117016010 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+62319A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117016010 | |||||||
| chr7:117016384 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+62693G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117016384 | |||||||
| chr7:117016410 | A | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+62719A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117016410 | |||||||
| chr7:117016504 | TTAAG | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.151+62817_151+6282 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117016504 | ||||||
| chr7:117017057 | A | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+63366A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017057 | |||||||
| chr7:117017060 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+63369C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017060 | |||||||
| chr7:117017410 | C | T | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+63719C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017410 | |||||||
| chr7:117017597 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+63906C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017597 | |||||||
| chr7:117017612 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.151+63921T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017612 | |||||||
| chr7:117017627 | T | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0178 |
2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.151+63936T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017627 | |||||||
| chr7:117017677 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.151+63986C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017677 | |||||||
| chr7:117017859 | A | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151+64168A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117017859 | |||||||
| chr7:117018112 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0042 |
2 | HG01192.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.151+64421G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117018112 | |||||||
| chr7:117018505 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.151+64814A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117018505 | |||||||
| chr7:117019163 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 |
3 | HG02717.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.151+65472G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117019163 | |||||||
| chr7:117019210 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.151+65519A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117019210 | |||||||
| chr7:117020119 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+66428G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020119 | |||||||
| chr7:117020139 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.151+66448G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020139 | |||||||
| chr7:117020410 | AC | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+66721delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117020410 | ||||||
| chr7:117020481 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.151+66790T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020481 | |||||||
| chr7:117020560 | T | C | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+66869T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020560 | |||||||
| chr7:117020646 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0184 |
3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.151+66955C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020646 | |||||||
| chr7:117020749 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+67058A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020749 | |||||||
| chr7:117020796 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151+67105T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020796 | |||||||
| chr7:117020797 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.151+67106A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020797 | |||||||
| chr7:117020856 | G | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(9): Show |
12 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+67165G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117020856 | |||||||
| chr7:117021109 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.151+67418G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021109 | |||||||
| chr7:117021113 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.151+67422G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021113 | |||||||
| chr7:117021468 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.151+67777A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021468 | |||||||
| chr7:117021795 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.151+68104T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021795 | |||||||
| chr7:117021952 | T | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+68261T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117021952 | |||||||
| chr7:117022054 | CT | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.151+68366delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117022054 | ||||||
| chr7:117022290 | G | A | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+68599G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022290 | |||||||
| chr7:117022336 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.151+68645C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022336 | |||||||
| chr7:117022458 | T | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+68767T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022458 | |||||||
| chr7:117022538 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.151+68847A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022538 | |||||||
| chr7:117022975 | T | C | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+69284T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117022975 | |||||||
| chr7:117023097 | G | GGAAATGT others(33): Show |
1 | a0001c0001t0001g0129 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.151+69407_151+6944 others(44): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023097 | ||||||
| chr7:117023777 | T | TTA | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.151+70102_151+7010 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023777 | ||||||
| chr7:117023777 | T | TTATA | 8 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0070 others(5): Show |
8 | HG00438.hp2 HG01192.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+70100_151+7010 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023777 | ||||||
| chr7:117023805 | C | CGT | 2 | a0001c0001t0001g0061 a0001c0001t0001g0129 |
2 | HG01358.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.151+70130_151+7013 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117023805 | ||||||
| chr7:117023934 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.151+70243C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117023934 | |||||||
| chr7:117023941 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+70250C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117023941 | |||||||
| chr7:117024067 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.151+70376A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024067 | |||||||
| chr7:117024092 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+70401G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024092 | |||||||
| chr7:117024673 | C | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.151+70982C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024673 | |||||||
| chr7:117024723 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+71032A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024723 | |||||||
| chr7:117024816 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.151+71125A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024816 | |||||||
| chr7:117024964 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.151+71273A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117024964 | |||||||
| chr7:117025000 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.151+71309A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025000 | |||||||
| chr7:117025536 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+71845G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025536 | |||||||
| chr7:117025537 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+71846C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025537 | |||||||
| chr7:117025732 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+72041C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117025732 | |||||||
| chr7:117026649 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.151+72958A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117026649 | |||||||
| chr7:117027121 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.152-72641T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027121 | |||||||
| chr7:117027132 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.152-72630A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027132 | |||||||
| chr7:117027355 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.152-72407G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027355 | |||||||
| chr7:117027446 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-72316G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027446 | |||||||
| chr7:117027462 | T | TAAAAGTA others(120): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | HG01433.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(131): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027462 | ||||||
| chr7:117027462 | T | TAAAAGTA others(115): Show |
1 | a0001c0001t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.152-72291_152-7229 others(126): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027462 | ||||||
| chr7:117027462 | T | TAAAAGTA others(110): Show |
1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(121): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027462 | ||||||
| chr7:117027463 | A | AAAAATTA others(24): Show |
1 | a0001c0001t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.152-72296_152-7229 others(35): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAATTA others(29): Show |
4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
4 | HG02622.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-72296_152-7229 others(40): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAATTA others(34): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(6): Show |
9 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-72296_152-7229 others(45): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAATTA others(44): Show |
1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.152-72296_152-7229 others(55): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(29): Show |
32 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-72266_152-7226 others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(28): Show |
3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 |
3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(39): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(37): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02451.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(48): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(42): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0092 |
2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.152-72291_152-7229 others(53): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(47): Show |
1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(58): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(27): Show |
1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-72291_152-7229 others(38): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(25): Show |
1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(36): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(40): Show |
1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-72291_152-7229 others(51): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(80): Show |
1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-72291_152-7229 others(91): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(3): Show |
16 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(13): Show |
16 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-72271_152-7226 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(8): Show |
10 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0154 others(7): Show |
10 | HG01255.hp1 HG01934.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-72276_152-7226 others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(13): Show |
28 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0073 others(25): Show |
28 | HG00323.hp2 HG00741.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.152-72281_152-7226 others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(18): Show |
33 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-72286_152-7226 others(29): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(23): Show |
18 | a0001c0001t0001g0074 a0001c0001t0001g0103 a0001c0001t0001g0105 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-72291_152-7226 others(34): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(28): Show |
7 | a0001c0001t0001g0071 a0001c0001t0001g0101 a0001c0001t0001g0107 others(4): Show |
7 | HG00738.hp1 HG00738.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-72296_152-7226 others(39): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027463 | A | AAAAGTAA others(33): Show |
1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-72262_152-7226 others(44): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027463 | ||||||
| chr7:117027473 | T | TAA | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-72287_152-7228 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117027473 | ||||||
| chr7:117027767 | G | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.152-71995G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027767 | |||||||
| chr7:117027930 | A | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-71832A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117027930 | |||||||
| chr7:117028608 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.152-71154T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117028608 | |||||||
| chr7:117028958 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.152-70804C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117028958 | |||||||
| chr7:117029234 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-70528T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029234 | |||||||
| chr7:117029239 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-70523C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029239 | |||||||
| chr7:117029241 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-70521A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029241 | |||||||
| chr7:117029641 | C | T | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-70121C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029641 | |||||||
| chr7:117029756 | A | AT | 75 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0064 others(72): Show |
75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.152-69994dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117029756 | ||||||
| chr7:117029861 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.152-69901C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029861 | |||||||
| chr7:117029889 | G | T | 1 | a0001c0001t0001g0032 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.152-69873G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117029889 | |||||||
| chr7:117030605 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(37): Show |
40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-69157A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030605 | |||||||
| chr7:117030620 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.152-69142A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030620 | |||||||
| chr7:117030637 | A | T | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.152-69125A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030637 | |||||||
| chr7:117030719 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.152-69043C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030719 | |||||||
| chr7:117030787 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.152-68975G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030787 | |||||||
| chr7:117030907 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-68855T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117030907 | |||||||
| chr7:117031128 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68634G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031128 | |||||||
| chr7:117031311 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-68451C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031311 | |||||||
| chr7:117031364 | G | GTGTGTAT others(27): Show |
8 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0085 others(5): Show |
8 | HG01071.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(38): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031364 | ||||||
| chr7:117031368 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0112 |
2 | HG03209.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.152-68394G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031368 | |||||||
| chr7:117031372 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0112 |
2 | HG03209.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.152-68390A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031372 | |||||||
| chr7:117031376 | G | GTGTGTAT others(7): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031376 | ||||||
| chr7:117031379 | T | TATATATA others(325): Show |
1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152-68377_152-6837 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031379 | ||||||
| chr7:117031379 | T | TATATATA others(653): Show |
1 | a0001c0001t0001g0079 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.152-68377_152-6837 others(664): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031379 | ||||||
| chr7:117031379 | T | TGTATATA others(177): Show |
1 | a0001c0001t0001g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(188): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(237): Show |
1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(248): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(505): Show |
1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(516): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(207): Show |
1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(218): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(267): Show |
4 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(87): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0144 |
2 | HG01358.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(98): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(117): Show |
1 | a0001c0001t0001g0182 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(128): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(137): Show |
1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(148): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(117): Show |
3 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0139 |
3 | HG00738.hp2 NA18971.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(128): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(387): Show |
1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(147): Show |
1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(158): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(267): Show |
3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0177 |
3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(297): Show |
2 | a0001c0001t0001g0154 a0001c0001t0001g0174 |
2 | HG01934.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(327): Show |
3 | a0001c0001t0001g0163 a0001c0001t0001g0172 a0001c0001t0001g0176 |
3 | NA18960.hp1 NA18988.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(357): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0159 |
2 | HG00323.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(368): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0162 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(237): Show |
3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0184 |
3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(248): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(267): Show |
1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(297): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0152 |
2 | HG02004.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(417): Show |
1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(428): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(327): Show |
5 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0167 others(2): Show |
5 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(357): Show |
4 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0122 others(1): Show |
4 | HG00099.hp1 HG00642.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(368): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(387): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0151 a0001c0001t0001g0164 others(2): Show |
5 | HG00323.hp1 HG01256.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(417): Show |
4 | a0001c0001t0001g0106 a0001c0001t0001g0156 a0001c0001t0001g0175 others(1): Show |
4 | HG02027.hp1 HG02083.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(428): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(447): Show |
3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0158 |
3 | HG02071.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(458): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(417): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(428): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(297): Show |
1 | a0001c0001t0001g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0149 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(447): Show |
1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(458): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(347): Show |
1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(358): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(347): Show |
1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(358): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(175): Show |
1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(186): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(357): Show |
1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(368): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(507): Show |
1 | a0001c0001t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(518): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(177): Show |
11 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(8): Show |
11 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(188): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(447): Show |
1 | a0001c0001t0001g0183 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(458): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(387): Show |
1 | a0001c0001t0001g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(297): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(308): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(327): Show |
1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(338): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(387): Show |
1 | a0001c0001t0001g0071 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(398): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(567): Show |
1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(578): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(117): Show |
1 | a0001c0001t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(128): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(55): Show |
1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(66): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(505): Show |
1 | a0001c0001t0001g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(516): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(535): Show |
1 | a0001c0001t0001g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(546): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(355): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(366): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(535): Show |
1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(546): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(595): Show |
1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(606): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(625): Show |
1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(636): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(385): Show |
1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(396): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(145): Show |
1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(156): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(265): Show |
1 | a0001c0001t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(276): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(325): Show |
1 | a0001c0001t0001g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(355): Show |
1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(366): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(445): Show |
1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(456): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(265): Show |
1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(276): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(325): Show |
1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(355): Show |
1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(366): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(385): Show |
4 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0109 others(1): Show |
4 | HG00738.hp1 HG01081.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(396): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(415): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0118 |
2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(426): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(325): Show |
1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(336): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(295): Show |
1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(306): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(235): Show |
1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(246): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(145): Show |
1 | a0001c0001t0001g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(156): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(175): Show |
1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(186): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(205): Show |
1 | a0001c0001t0001g0032 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(216): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(295): Show |
1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(306): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(235): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0023 others(4): Show |
7 | HG01256.hp1 HG02071.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(246): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(265): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0029 others(6): Show |
9 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(276): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(295): Show |
1 | a0001c0001t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.152-68383_152-6838 others(306): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(175): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0017 |
2 | HG01255.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(186): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(205): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0019 others(3): Show |
6 | HG00673.hp2 HG01943.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(216): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(385): Show |
1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(396): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(235): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(4): Show |
7 | HG00642.hp1 HG02040.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68383_152-6838 others(246): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(263): Show |
1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.152-68383_152-6838 others(274): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031379 | T | TGTATATA others(233): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.152-68383_152-6838 others(244): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031379 | |||||||
| chr7:117031380 | A | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68382A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031380 | |||||||
| chr7:117031383 | TATGTGTA others(49): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68376_152-6832 others(60): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031383 | ||||||
| chr7:117031384 | ATGTG | A | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68376_152-6837 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031384 | ||||||
| chr7:117031386 | G | A | 9 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0085 others(6): Show |
9 | HG01071.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68376G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031386 | |||||||
| chr7:117031387 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68375T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031387 | |||||||
| chr7:117031389 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.152-68373T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031389 | |||||||
| chr7:117031390 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.152-68372A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031390 | |||||||
| chr7:117031391 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68371T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031391 | |||||||
| chr7:117031392 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0143 |
2 | HG00738.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.152-68370A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031392 | |||||||
| chr7:117031394 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68368A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031394 | |||||||
| chr7:117031397 | T | C | 10 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0048 others(7): Show |
10 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-68365T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031397 | |||||||
| chr7:117031397 | TGCATATA others(5): Show |
T | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68364_152-6835 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031397 | |||||||
| chr7:117031399 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01433.hp2 HG02055.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-68363C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031399 | |||||||
| chr7:117031400 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68362A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031400 | |||||||
| chr7:117031404 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68358A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031404 | |||||||
| chr7:117031406 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68356A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031406 | |||||||
| chr7:117031407 | C | CGCATATA others(143): Show |
1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152-68263_152-6811 others(154): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | ||||||
| chr7:117031407 | C | CGCATATA others(171): Show |
1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-68354_152-6817 others(182): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | ||||||
| chr7:117031407 | C | CGCATATA others(231): Show |
1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.152-68177_152-6817 others(242): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | ||||||
| chr7:117031407 | C | CGCATATA others(171): Show |
1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.152-68207_152-6820 others(182): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031407 | ||||||
| chr7:117031407 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68355C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031407 | |||||||
| chr7:117031409 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68353C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031409 | |||||||
| chr7:117031416 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152-68346G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031416 | |||||||
| chr7:117031417 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68345T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031417 | |||||||
| chr7:117031419 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.152-68343T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031419 | |||||||
| chr7:117031420 | G | A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68342G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031420 | |||||||
| chr7:117031421 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68341T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031421 | |||||||
| chr7:117031422 | A | G | 5 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0139 others(2): Show |
5 | HG00738.hp2 NA18747.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-68340A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031422 | |||||||
| chr7:117031424 | A | G | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68338A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031424 | |||||||
| chr7:117031427 | T | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(9): Show |
12 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68335T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031427 | |||||||
| chr7:117031428 | GCATATAT others(5): Show |
G | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68333_152-6832 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031428 | |||||||
| chr7:117031430 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68332A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031430 | |||||||
| chr7:117031437 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.152-68325T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031437 | |||||||
| chr7:117031437 | T | TATGCGCA others(7): Show |
1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68325_152-6832 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031437 | |||||||
| chr7:117031446 | G | A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68316G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031446 | |||||||
| chr7:117031447 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68315T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031447 | |||||||
| chr7:117031449 | T | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0182 |
3 | HG02293.hp2 HG02300.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.152-68313T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031449 | |||||||
| chr7:117031450 | G | A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68312G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031450 | |||||||
| chr7:117031451 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.152-68311T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031451 | |||||||
| chr7:117031452 | A | G | 6 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0136 others(3): Show |
6 | HG00738.hp2 HG01358.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-68310A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031452 | |||||||
| chr7:117031457 | T | C | 10 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(7): Show |
10 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-68305T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031457 | |||||||
| chr7:117031460 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68302A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031460 | |||||||
| chr7:117031465 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-68297T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031465 | |||||||
| chr7:117031466 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68296A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031466 | |||||||
| chr7:117031467 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.152-68295T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031467 | |||||||
| chr7:117031469 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68293C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031469 | |||||||
| chr7:117031470 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68292A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031470 | |||||||
| chr7:117031476 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68286G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031476 | |||||||
| chr7:117031477 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68285T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031477 | |||||||
| chr7:117031480 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-68282G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031480 | |||||||
| chr7:117031482 | A | G | 7 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00738.hp2 HG01358.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68280A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031482 | |||||||
| chr7:117031487 | T | C | 9 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68275T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031487 | |||||||
| chr7:117031490 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68272A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031490 | |||||||
| chr7:117031495 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-68267T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031495 | |||||||
| chr7:117031497 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68265T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031497 | |||||||
| chr7:117031507 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68255T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031507 | |||||||
| chr7:117031512 | A | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68250A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031512 | |||||||
| chr7:117031517 | T | C | 9 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-68245T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031517 | |||||||
| chr7:117031520 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68242A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031520 | |||||||
| chr7:117031525 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0089 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-68237T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031525 | |||||||
| chr7:117031527 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68235T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031527 | |||||||
| chr7:117031537 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68225T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031537 | |||||||
| chr7:117031542 | A | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68220A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031542 | |||||||
| chr7:117031547 | T | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68215T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031547 | |||||||
| chr7:117031550 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68212A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031550 | |||||||
| chr7:117031555 | T | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG02451.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-68207T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031555 | |||||||
| chr7:117031557 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68205T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031557 | |||||||
| chr7:117031567 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68195T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031567 | |||||||
| chr7:117031572 | A | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
9 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-68190A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031572 | |||||||
| chr7:117031577 | T | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68185T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031577 | |||||||
| chr7:117031580 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68182A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031580 | |||||||
| chr7:117031585 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68177T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031585 | |||||||
| chr7:117031587 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68175T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031587 | |||||||
| chr7:117031597 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.152-68165T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031597 | |||||||
| chr7:117031602 | A | G | 7 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00738.hp2 HG01071.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-68160A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031602 | |||||||
| chr7:117031607 | T | C | 7 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-68155T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031607 | |||||||
| chr7:117031610 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68152A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031610 | |||||||
| chr7:117031615 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68147T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031615 | |||||||
| chr7:117031617 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68145T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031617 | |||||||
| chr7:117031619 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68143C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031619 | |||||||
| chr7:117031627 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.152-68135T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031627 | |||||||
| chr7:117031632 | A | G | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG01071.hp1 HG01358.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-68130A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031632 | |||||||
| chr7:117031637 | T | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-68125T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031637 | |||||||
| chr7:117031640 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-68122A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031640 | |||||||
| chr7:117031645 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68117T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031645 | |||||||
| chr7:117031647 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68115T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031647 | |||||||
| chr7:117031649 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-68113T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031649 | |||||||
| chr7:117031654 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68107_152-6809 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031654 | |||||||
| chr7:117031657 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.152-68105T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031657 | |||||||
| chr7:117031662 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0132 |
3 | HG01071.hp1 HG02683.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.152-68100A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031662 | |||||||
| chr7:117031667 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0053 |
3 | HG02280.hp2 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.152-68095T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031667 | |||||||
| chr7:117031670 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0049 |
2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.152-68092A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031670 | |||||||
| chr7:117031671 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68091T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031671 | |||||||
| chr7:117031672 | A | ATACACGC others(11): Show |
1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68088_152-6808 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031672 | ||||||
| chr7:117031673 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-68089T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031673 | |||||||
| chr7:117031676 | A | ACGCATAT others(5): Show |
76 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0053 others(73): Show |
76 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.152-68086_152-6808 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031676 | |||||||
| chr7:117031676 | A | ACGCATAT others(97): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68086_152-6808 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031676 | |||||||
| chr7:117031677 | T | C | 31 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(28): Show |
31 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.152-68085T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031677 | |||||||
| chr7:117031678 | G | GCATATAT others(195): Show |
1 | a0001c0001t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152-68084_152-6808 others(206): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031678 | |||||||
| chr7:117031679 | T | C | 40 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.152-68083T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031679 | |||||||
| chr7:117031682 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-68080A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031682 | |||||||
| chr7:117031683 | TACAC | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0056 others(1): Show |
4 | HG02486.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-68075_152-6807 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031683 | ||||||
| chr7:117031683 | TACACAC | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68077_152-6807 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031683 | ||||||
| chr7:117031684 | A | ATGTGTGT others(7): Show |
12 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0001g0131 others(9): Show |
12 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68078_152-6807 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | |||||||
| chr7:117031684 | A | ATGTGTGT others(97): Show |
1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.152-68078_152-6807 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | |||||||
| chr7:117031684 | A | ATGTGTGT others(127): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0142 |
2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.152-68078_152-6807 others(138): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | |||||||
| chr7:117031684 | A | ATGTGTGT others(125): Show |
1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.152-68078_152-6807 others(136): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | |||||||
| chr7:117031684 | A | ATGTGTGT others(97): Show |
1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152-68078_152-6807 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | |||||||
| chr7:117031684 | A | ATGTGTGT others(97): Show |
1 | a0001c0001t0001g0127 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.152-68078_152-6807 others(108): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | |||||||
| chr7:117031684 | A | G | 77 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0053 others(74): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.152-68078A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031684 | |||||||
| chr7:117031685 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0053 others(74): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.152-68077C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031685 | |||||||
| chr7:117031686 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0050 others(75): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.152-68076A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031686 | |||||||
| chr7:117031687 | C | T | 20 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(17): Show |
20 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-68075C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031687 | |||||||
| chr7:117031688 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0125 |
3 | HG02258.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-68074A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031688 | |||||||
| chr7:117031689 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0045 others(98): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.152-68073C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031689 | |||||||
| chr7:117031690 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0056 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-68072A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031690 | |||||||
| chr7:117031692 | A | G | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68070A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031692 | |||||||
| chr7:117031693 | T | C | 19 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-68069T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031693 | |||||||
| chr7:117031693 | T | TACGC | 76 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0053 others(73): Show |
76 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.152-68069_152-6806 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031693 | |||||||
| chr7:117031694 | G | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0053 others(73): Show |
76 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.152-68068G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031694 | |||||||
| chr7:117031695 | T | C | 18 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-68067T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031695 | |||||||
| chr7:117031696 | A | G | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68066A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031696 | |||||||
| chr7:117031700 | A | ATG | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(37): Show |
40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-68058_152-6805 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031700 | ||||||
| chr7:117031700 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0045 others(79): Show |
82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.152-68062A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031700 | |||||||
| chr7:117031703 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0048 others(2): Show |
5 | HG02258.hp1 HG02258.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-68059T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031703 | |||||||
| chr7:117031704 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0125 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.152-68058G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031704 | |||||||
| chr7:117031704 | G | GCA | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-68058_152-6805 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031704 | |||||||
| chr7:117031704 | G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-68032_152-6802 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031704 | ||||||
| chr7:117031705 | TATATATG others(1): Show |
T | 32 | a0001c0001t0001g0015 a0001c0001t0001g0065 a0001c0001t0001g0069 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-68050_152-6804 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031705 | ||||||
| chr7:117031706 | A | G | 18 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(15): Show |
18 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-68056A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031706 | |||||||
| chr7:117031710 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.152-68052A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031710 | |||||||
| chr7:117031711 | T | C | 11 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
11 | HG02258.hp2 HG02486.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-68051T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031711 | |||||||
| chr7:117031713 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0125 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.152-68049C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031713 | |||||||
| chr7:117031714 | A | ATATATGT others(3): Show |
8 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(5): Show |
8 | HG02486.hp2 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68043_152-6804 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031714 | ||||||
| chr7:117031714 | A | G | 33 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0065 others(30): Show |
33 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-68048A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031714 | |||||||
| chr7:117031719 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-68043T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031719 | |||||||
| chr7:117031720 | A | G | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68042A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031720 | |||||||
| chr7:117031721 | T | C | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
11 | HG01358.hp1 HG01433.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-68041T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031721 | |||||||
| chr7:117031723 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0045 others(76): Show |
79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.152-68039C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031723 | |||||||
| chr7:117031724 | A | ATATATGT others(3): Show |
1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-68033_152-6803 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031724 | ||||||
| chr7:117031724 | A | G | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02258.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-68038A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031724 | |||||||
| chr7:117031727 | T | TACACAC | 90 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0066 others(87): Show |
90 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.152-68034_152-6803 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031727 | ||||||
| chr7:117031730 | A | G | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0053 others(5): Show |
8 | HG01358.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-68032A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031730 | |||||||
| chr7:117031731 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-68031T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031731 | |||||||
| chr7:117031733 | C | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0055 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.152-68029C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031733 | |||||||
| chr7:117031733 | CATATATG others(3): Show |
C | 33 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0065 others(30): Show |
33 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-68022_152-6801 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031733 | ||||||
| chr7:117031734 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(41): Show |
44 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.152-68028A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031734 | |||||||
| chr7:117031740 | G | A | 14 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG01358.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-68022G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031740 | |||||||
| chr7:117031743 | T | C | 16 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(13): Show |
16 | HG01358.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-68019T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031743 | |||||||
| chr7:117031744 | A | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(102): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.152-68018A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031744 | |||||||
| chr7:117031751 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0068 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-68011T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031751 | |||||||
| chr7:117031754 | A | G | 47 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(44): Show |
47 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.152-68008A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031754 | |||||||
| chr7:117031758 | A | ATG | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-68000_152-6799 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031758 | ||||||
| chr7:117031760 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(89): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.152-68002G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031760 | |||||||
| chr7:117031763 | T | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(89): Show |
92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.152-67999T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031763 | |||||||
| chr7:117031764 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG02055.hp2 HG02280.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-67998A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031764 | |||||||
| chr7:117031770 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0068 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67992A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031770 | |||||||
| chr7:117031774 | A | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0048 others(92): Show |
95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.152-67988A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031774 | |||||||
| chr7:117031778 | A | ATG | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(36): Show |
39 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.152-67980_152-6797 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031778 | ||||||
| chr7:117031780 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0068 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67982G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031780 | |||||||
| chr7:117031781 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0068 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67981T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031781 | |||||||
| chr7:117031783 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0055 a0001c0001t0001g0068 |
3 | HG02622.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67979T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031783 | |||||||
| chr7:117031784 | A | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0106 a0001c0001t0001g0113 others(1): Show |
4 | HG02615.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-67978A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031784 | |||||||
| chr7:117031790 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0068 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152-67972A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031790 | |||||||
| chr7:117031793 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67969C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031793 | |||||||
| chr7:117031794 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0055 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.152-67968A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031794 | |||||||
| chr7:117031796 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67966A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031796 | |||||||
| chr7:117031798 | ATG | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(61): Show |
64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.152-67958_152-6795 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031798 | ||||||
| chr7:117031800 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67962G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031800 | |||||||
| chr7:117031803 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67959T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031803 | |||||||
| chr7:117031804 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67958G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031804 | |||||||
| chr7:117031804 | GTA | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0122 others(32): Show |
35 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.152-67950_152-6794 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031804 | ||||||
| chr7:117031805 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67957T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031805 | |||||||
| chr7:117031806 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-67956A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031806 | |||||||
| chr7:117031807 | T | TATATGC | 32 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-67951_152-6795 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031807 | ||||||
| chr7:117031810 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.152-67952A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031810 | |||||||
| chr7:117031813 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67949T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031813 | |||||||
| chr7:117031815 | C | T | 33 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0001g0066 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-67947C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031815 | |||||||
| chr7:117031816 | A | G | 33 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0001g0066 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.152-67946A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031816 | |||||||
| chr7:117031816 | ATATATC | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0113 |
3 | HG01433.hp2 HG02109.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.152-67906_152-6790 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031816 | ||||||
| chr7:117031816 | ATATATCT others(5): Show |
A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-67912_152-6790 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031816 | ||||||
| chr7:117031818 | A | ATATGTGT others(1): Show |
21 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0126 others(18): Show |
21 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.152-67941_152-6794 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031818 | ||||||
| chr7:117031818 | A | G | 32 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.152-67944A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031818 | |||||||
| chr7:117031820 | A | ATGTG | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
66 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.152-67941_152-6794 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031820 | ||||||
| chr7:117031820 | ATC | A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67940_152-6793 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031820 | ||||||
| chr7:117031822 | C | A | 54 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(51): Show |
54 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.152-67940C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031822 | |||||||
| chr7:117031822 | C | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
66 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.152-67940C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031822 | |||||||
| chr7:117031824 | A | G | 13 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67938A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031824 | |||||||
| chr7:117031826 | A | G | 14 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(11): Show |
14 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-67936A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031826 | |||||||
| chr7:117031827 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-67935T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031827 | |||||||
| chr7:117031827 | T | TGC | 53 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0064 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.152-67935_152-6793 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031827 | |||||||
| chr7:117031828 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.152-67934C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031828 | |||||||
| chr7:117031828 | C | G | 13 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67934C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031828 | |||||||
| chr7:117031830 | ATATCTAT others(21): Show |
A | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.152-67924_152-6789 others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031830 | ||||||
| chr7:117031832 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
65 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.152-67930A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031832 | |||||||
| chr7:117031833 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
65 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.152-67929T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031833 | |||||||
| chr7:117031834 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
78 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.152-67928C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031834 | |||||||
| chr7:117031838 | A | G | 13 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67924A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031838 | |||||||
| chr7:117031839 | T | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67923T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031839 | |||||||
| chr7:117031840 | C | A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67922C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031840 | |||||||
| chr7:117031846 | CTATATCT others(1): Show |
C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0106 others(4): Show |
7 | HG01358.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-67912_152-6790 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031846 | ||||||
| chr7:117031852 | CTA | C | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-67906_152-6790 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031852 | ||||||
| chr7:117031854 | ATATC | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0027 others(10): Show |
13 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152-67892_152-6788 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031854 | ||||||
| chr7:117031858 | C | CTA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(25): Show |
28 | HG00642.hp1 HG00673.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.152-67902_152-6790 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031858 | ||||||
| chr7:117031868 | ATC | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0114 |
2 | HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.152-67892_152-6789 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031868 | ||||||
| chr7:117031870 | C | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0001g0059 others(13): Show |
16 | HG01358.hp1 HG02055.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.152-67892C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031870 | |||||||
| chr7:117031880 | ATAT | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
8 | HG01358.hp1 HG02071.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-67880_152-6787 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031880 | ||||||
| chr7:117031882 | ATTT | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0085 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-67866_152-6786 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117031882 | ||||||
| chr7:117031883 | T | TA | 22 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-67879_152-6787 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031883 | |||||||
| chr7:117031884 | T | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.152-67878T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031884 | |||||||
| chr7:117031885 | T | A | 12 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0133 others(9): Show |
12 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-67877T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031885 | |||||||
| chr7:117031886 | T | A | 39 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0068 others(36): Show |
39 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.152-67876T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031886 | |||||||
| chr7:117031887 | T | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0125 |
3 | HG02258.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152-67875T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031887 | |||||||
| chr7:117031888 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0026 |
2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.152-67874T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117031888 | |||||||
| chr7:117032140 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.152-67622C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032140 | |||||||
| chr7:117032386 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.152-67376G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032386 | |||||||
| chr7:117032533 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152-67229C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032533 | |||||||
| chr7:117032710 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.152-67052G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032710 | |||||||
| chr7:117032776 | A | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-66986A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117032776 | |||||||
| chr7:117033296 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0184 |
3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-66466G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033296 | |||||||
| chr7:117033419 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152-66343G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033419 | |||||||
| chr7:117033420 | CT | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-66328delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117033420 | ||||||
| chr7:117033441 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152-66321G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033441 | |||||||
| chr7:117033480 | G | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.152-66282G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033480 | |||||||
| chr7:117033577 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-66185C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033577 | |||||||
| chr7:117033635 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-66127T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033635 | |||||||
| chr7:117033815 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.152-65947A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033815 | |||||||
| chr7:117033838 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.152-65924G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033838 | |||||||
| chr7:117033848 | A | G | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-65914A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117033848 | |||||||
| chr7:117034182 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-65580T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034182 | |||||||
| chr7:117034794 | T | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG00673.hp2 HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-64968T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034794 | |||||||
| chr7:117034821 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152-64941C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034821 | |||||||
| chr7:117034969 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.152-64793C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117034969 | |||||||
| chr7:117035041 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.152-64721A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035041 | |||||||
| chr7:117035215 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.152-64547C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035215 | |||||||
| chr7:117035296 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152-64466T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035296 | |||||||
| chr7:117035441 | G | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-64321G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035441 | |||||||
| chr7:117035587 | C | T | 13 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-64175C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117035587 | |||||||
| chr7:117035819 | CT | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0065 others(68): Show |
71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.152-63932delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117035819 | ||||||
| chr7:117036025 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.152-63737G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036025 | |||||||
| chr7:117036042 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152-63720A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036042 | |||||||
| chr7:117036059 | T | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-63703T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036059 | |||||||
| chr7:117036256 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0122 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.152-63506C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036256 | |||||||
| chr7:117036315 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-63447C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036315 | |||||||
| chr7:117036375 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-63387T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036375 | |||||||
| chr7:117036825 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.152-62937C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036825 | |||||||
| chr7:117036922 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.152-62840G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117036922 | |||||||
| chr7:117037051 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.152-62711G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037051 | |||||||
| chr7:117037123 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-62639A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037123 | |||||||
| chr7:117037124 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-62638C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037124 | |||||||
| chr7:117037472 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-62290C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037472 | |||||||
| chr7:117037495 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-62267C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037495 | |||||||
| chr7:117037643 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(2): Show |
5 | HG02257.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-62119C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037643 | |||||||
| chr7:117037651 | T | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 |
3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152-62111T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117037651 | |||||||
| chr7:117038056 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0063 |
2 | HG01433.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-61706T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038056 | |||||||
| chr7:117038202 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-61560G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038202 | |||||||
| chr7:117038276 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-61486C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038276 | |||||||
| chr7:117038542 | A | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-61220A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038542 | |||||||
| chr7:117038585 | G | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-61177G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038585 | |||||||
| chr7:117038683 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152-61079T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117038683 | |||||||
| chr7:117039033 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-60729T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039033 | |||||||
| chr7:117039246 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.152-60516C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039246 | |||||||
| chr7:117039580 | CA | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-60166delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117039580 | ||||||
| chr7:117039638 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-60124A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039638 | |||||||
| chr7:117039957 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-59805A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117039957 | |||||||
| chr7:117040244 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-59518C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040244 | |||||||
| chr7:117040388 | A | G | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-59374A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040388 | |||||||
| chr7:117040625 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.152-59137G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040625 | |||||||
| chr7:117040777 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-58985A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117040777 | |||||||
| chr7:117041073 | G | C | 15 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(12): Show |
15 | HG01433.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-58689G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041073 | |||||||
| chr7:117041554 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152-58208G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041554 | |||||||
| chr7:117041677 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.152-58085C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041677 | |||||||
| chr7:117041849 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.152-57913T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041849 | |||||||
| chr7:117041966 | G | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0137 |
3 | HG02040.hp1 HG02523.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.152-57796G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117041966 | |||||||
| chr7:117042030 | A | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-57732A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117042030 | |||||||
| chr7:117042047 | T | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-57715T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117042047 | |||||||
| chr7:117042128 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.152-57634A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117042128 | |||||||
| chr7:117043370 | T | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-56392T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117043370 | |||||||
| chr7:117043587 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.152-56175A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117043587 | |||||||
| chr7:117044142 | T | A | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-55620T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044142 | |||||||
| chr7:117044321 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152-55441C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044321 | |||||||
| chr7:117044323 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-55439G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044323 | |||||||
| chr7:117044343 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0104 |
2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.152-55419A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044343 | |||||||
| chr7:117044380 | C | T | 74 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.152-55382C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044380 | |||||||
| chr7:117044608 | CT | C | 22 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-55153delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044608 | |||||||
| chr7:117044968 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-54794C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117044968 | |||||||
| chr7:117045567 | G | T | 61 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(58): Show |
61 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.152-54195G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117045567 | |||||||
| chr7:117046239 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(39): Show |
42 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.152-53523G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046239 | |||||||
| chr7:117046401 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152-53361C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046401 | |||||||
| chr7:117046574 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-53188C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046574 | |||||||
| chr7:117046798 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.152-52964T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046798 | |||||||
| chr7:117046940 | A | G | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
6 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-52822A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046940 | |||||||
| chr7:117046980 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-52782C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117046980 | |||||||
| chr7:117047047 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-52715A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047047 | |||||||
| chr7:117047107 | C | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0188 |
3 | HG02280.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-52655C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047107 | |||||||
| chr7:117047136 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-52626C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047136 | |||||||
| chr7:117047277 | G | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-52485G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047277 | |||||||
| chr7:117047744 | C | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0122 |
3 | HG02615.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152-52018C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117047744 | |||||||
| chr7:117048540 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.152-51222G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117048540 | |||||||
| chr7:117048926 | T | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0184 |
3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-50836T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117048926 | |||||||
| chr7:117048966 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-50796G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117048966 | |||||||
| chr7:117049274 | A | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-50488A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117049274 | |||||||
| chr7:117049287 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0152 |
2 | HG00642.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.152-50475G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117049287 | |||||||
| chr7:117049977 | C | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152-49785C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117049977 | |||||||
| chr7:117050023 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0147 others(28): Show |
31 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.152-49739G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050023 | |||||||
| chr7:117050047 | A | G | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-49715A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050047 | |||||||
| chr7:117050050 | C | CA | 9 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0058 others(6): Show |
9 | HG00323.hp1 HG01433.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-49696dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050050 | ||||||
| chr7:117050050 | CA | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0064 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.152-49696delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050050 | ||||||
| chr7:117050070 | C | G | 14 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(11): Show |
14 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.152-49692C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050070 | |||||||
| chr7:117050139 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152-49623C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050139 | |||||||
| chr7:117050214 | C | CA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(37): Show |
40 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-49534dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050214 | ||||||
| chr7:117050632 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.152-49130T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050632 | |||||||
| chr7:117050772 | T | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-48990T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117050772 | |||||||
| chr7:117050928 | C | CA | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(2): Show |
5 | HG02818.hp1 HG02922.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-48817dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050928 | ||||||
| chr7:117050928 | CA | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.152-48817delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117050928 | ||||||
| chr7:117051041 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-48721C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117051041 | |||||||
| chr7:117051528 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-48234G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117051528 | |||||||
| chr7:117051954 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-47808C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117051954 | |||||||
| chr7:117052600 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(3): Show |
6 | HG01433.hp2 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-47162C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052600 | |||||||
| chr7:117052872 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.152-46890C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052872 | |||||||
| chr7:117052904 | A | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-46858A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052904 | |||||||
| chr7:117052912 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-46850C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052912 | |||||||
| chr7:117052920 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152-46842C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117052920 | |||||||
| chr7:117053041 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-46721A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053041 | |||||||
| chr7:117053105 | GTTGT | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01081.hp1 HG02257.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.152-46651_152-4664 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117053105 | ||||||
| chr7:117053266 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.152-46496C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053266 | |||||||
| chr7:117053328 | A | G | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-46434A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053328 | |||||||
| chr7:117053377 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-46385G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053377 | |||||||
| chr7:117053431 | C | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-46331C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053431 | |||||||
| chr7:117053607 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.152-46155C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053607 | |||||||
| chr7:117053688 | G | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0127 others(6): Show |
9 | HG00738.hp2 HG01071.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-46074G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053688 | |||||||
| chr7:117053736 | A | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-46026A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053736 | |||||||
| chr7:117053756 | T | G | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-46006T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053756 | |||||||
| chr7:117053848 | C | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
15 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-45914C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053848 | |||||||
| chr7:117053850 | GT | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.152-45899delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117053850 | ||||||
| chr7:117053886 | C | T | 12 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-45876C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053886 | |||||||
| chr7:117053928 | C | T | 12 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0086 others(9): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-45834C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117053928 | |||||||
| chr7:117054214 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.152-45548G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117054214 | |||||||
| chr7:117054682 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-45080G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117054682 | |||||||
| chr7:117054874 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.152-44888A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117054874 | |||||||
| chr7:117055227 | G | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-44535G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055227 | |||||||
| chr7:117055235 | C | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-44527C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055235 | |||||||
| chr7:117055440 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-44322G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055440 | |||||||
| chr7:117055588 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-44174A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055588 | |||||||
| chr7:117055590 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-44172C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117055590 | |||||||
| chr7:117056343 | A | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.152-43419A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056343 | |||||||
| chr7:117056366 | G | A | 23 | a0001c0001t0001g0017 a0001c0001t0001g0125 a0001c0001t0001g0126 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-43396G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056366 | |||||||
| chr7:117056367 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.152-43395G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056367 | |||||||
| chr7:117056372 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-43390T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056372 | |||||||
| chr7:117056527 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-43235C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056527 | |||||||
| chr7:117056621 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152-43141C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056621 | |||||||
| chr7:117056867 | G | A | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
18 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-42895G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117056867 | |||||||
| chr7:117057028 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.152-42734A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117057028 | |||||||
| chr7:117057034 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.152-42728G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117057034 | |||||||
| chr7:117057473 | A | G | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-42289A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117057473 | |||||||
| chr7:117058071 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-41691T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117058071 | |||||||
| chr7:117058413 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-41349A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117058413 | |||||||
| chr7:117058872 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(2): Show |
5 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-40890A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117058872 | |||||||
| chr7:117059033 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0098 |
2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.152-40729T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059033 | |||||||
| chr7:117059408 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.152-40354G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059408 | |||||||
| chr7:117059807 | C | CA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
62 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.152-39929dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117059807 | ||||||
| chr7:117059898 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.152-39864G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059898 | |||||||
| chr7:117059944 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-39818C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117059944 | |||||||
| chr7:117060137 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.152-39625G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060137 | |||||||
| chr7:117060207 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0063 |
2 | HG01433.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-39555G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060207 | |||||||
| chr7:117060793 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152-38969G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060793 | |||||||
| chr7:117060875 | G | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-38887G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117060875 | |||||||
| chr7:117061303 | T | G | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-38459T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061303 | |||||||
| chr7:117061706 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(5): Show |
8 | HG02040.hp2 HG02273.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-38056T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061706 | |||||||
| chr7:117061754 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(22): Show |
25 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.152-38008G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061754 | |||||||
| chr7:117061767 | C | G | 1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-37995C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117061767 | |||||||
| chr7:117062126 | A | G | 6 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-37636A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117062126 | |||||||
| chr7:117062673 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.152-37089T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117062673 | |||||||
| chr7:117062696 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0042 |
2 | HG01192.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.152-37066A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117062696 | |||||||
| chr7:117063506 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.152-36256C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063506 | |||||||
| chr7:117063511 | C | T | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-36251C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063511 | |||||||
| chr7:117063596 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.152-36166C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063596 | |||||||
| chr7:117063965 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.152-35797C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117063965 | |||||||
| chr7:117064171 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.152-35591C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117064171 | |||||||
| chr7:117064188 | GT | G | 12 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-35566delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117064188 | ||||||
| chr7:117064428 | C | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-35334C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117064428 | |||||||
| chr7:117064630 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.152-35132C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117064630 | |||||||
| chr7:117065164 | A | G | 63 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0045 others(60): Show |
63 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.152-34598A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065164 | |||||||
| chr7:117065176 | A | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-34586A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065176 | |||||||
| chr7:117065204 | C | CT | 5 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0112 others(2): Show |
5 | HG00438.hp2 HG01433.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-34535dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117065204 | ||||||
| chr7:117065204 | CT | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.152-34535delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117065204 | ||||||
| chr7:117065489 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.152-34273G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065489 | |||||||
| chr7:117065790 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-33972T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065790 | |||||||
| chr7:117065799 | C | T | 23 | a0001c0001t0001g0017 a0001c0001t0001g0125 a0001c0001t0001g0126 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-33963C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117065799 | |||||||
| chr7:117066486 | G | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | HG01496.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.152-33276G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066486 | |||||||
| chr7:117066685 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0112 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-33077T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066685 | |||||||
| chr7:117066709 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-33053C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066709 | |||||||
| chr7:117066764 | C | CA | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(43): Show |
46 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.152-32975dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117066764 | ||||||
| chr7:117066764 | CA | C | 16 | a0001c0001t0001g0057 a0001c0001t0001g0064 a0001c0001t0001g0065 others(13): Show |
16 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-32975delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117066764 | ||||||
| chr7:117066866 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.152-32896C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117066866 | |||||||
| chr7:117067041 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.152-32721G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067041 | |||||||
| chr7:117067082 | C | T | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-32680C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067082 | |||||||
| chr7:117067701 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152-32061A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067701 | |||||||
| chr7:117067857 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-31905C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067857 | |||||||
| chr7:117067972 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.152-31790G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117067972 | |||||||
| chr7:117068103 | A | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-31659A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117068103 | |||||||
| chr7:117069464 | C | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0159 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.152-30298C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069464 | |||||||
| chr7:117069516 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(37): Show |
40 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.152-30246C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069516 | |||||||
| chr7:117069685 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.152-30077A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069685 | |||||||
| chr7:117069704 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-30058C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117069704 | |||||||
| chr7:117070336 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-29426G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070336 | |||||||
| chr7:117070403 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.152-29359C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070403 | |||||||
| chr7:117070531 | T | TTTTG | 5 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(2): Show |
5 | HG02280.hp1 HG02683.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-29207_152-2920 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117070531 | ||||||
| chr7:117070531 | TTTTG | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0074 others(10): Show |
13 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-29207_152-2920 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117070531 | ||||||
| chr7:117070580 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-29182C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070580 | |||||||
| chr7:117070702 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.152-29060T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117070702 | |||||||
| chr7:117071111 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-28651C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117071111 | |||||||
| chr7:117071123 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0187 |
3 | NA19000.hp1 NA19004.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.152-28639A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117071123 | |||||||
| chr7:117071180 | C | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-28582C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117071180 | |||||||
| chr7:117072214 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.152-27548C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072214 | |||||||
| chr7:117072586 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-27176A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072586 | |||||||
| chr7:117072637 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.152-27125G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072637 | |||||||
| chr7:117072833 | G | A | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
18 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-26929G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072833 | |||||||
| chr7:117072841 | T | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-26921T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117072841 | |||||||
| chr7:117073595 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-26167T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117073595 | |||||||
| chr7:117073631 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-26131C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117073631 | |||||||
| chr7:117073731 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-26031A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117073731 | |||||||
| chr7:117074260 | G | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-25502G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117074260 | |||||||
| chr7:117074489 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02273.hp1 HG02615.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-25273C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117074489 | |||||||
| chr7:117074792 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02486.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.152-24970T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117074792 | |||||||
| chr7:117075262 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.152-24500G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117075262 | |||||||
| chr7:117075814 | A | G | 23 | a0001c0001t0001g0017 a0001c0001t0001g0125 a0001c0001t0001g0126 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-23948A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117075814 | |||||||
| chr7:117075953 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-23809C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117075953 | |||||||
| chr7:117076389 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-23373T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076389 | |||||||
| chr7:117076544 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(31): Show |
34 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-23218G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076544 | |||||||
| chr7:117076663 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0103 |
2 | HG00741.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.152-23099C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076663 | |||||||
| chr7:117076746 | C | T | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-23016C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076746 | |||||||
| chr7:117076854 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 |
3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-22908C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076854 | |||||||
| chr7:117076894 | A | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(31): Show |
34 | HG00323.hp2 HG00438.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-22868A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117076894 | |||||||
| chr7:117077110 | G | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-22652G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077110 | |||||||
| chr7:117077242 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-22520A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077242 | |||||||
| chr7:117077495 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-22267G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077495 | |||||||
| chr7:117077563 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-22199T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077563 | |||||||
| chr7:117077844 | C | CT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(2): Show |
5 | HG02630.hp2 HG03139.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.152-21899dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117077844 | ||||||
| chr7:117077844 | CT | C | 46 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0043 others(43): Show |
46 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.152-21899delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117077844 | ||||||
| chr7:117077858 | T | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(8): Show |
11 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-21904T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077858 | |||||||
| chr7:117077912 | C | T | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-21850C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117077912 | |||||||
| chr7:117078422 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-21340T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117078422 | |||||||
| chr7:117078681 | A | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-21081A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117078681 | |||||||
| chr7:117078904 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(32): Show |
35 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.152-20858C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117078904 | |||||||
| chr7:117079196 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-20566C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117079196 | |||||||
| chr7:117079235 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.152-20527G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117079235 | |||||||
| chr7:117079968 | C | CT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.152-19764dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | ||||||
| chr7:117079968 | C | CTT | 8 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0079 others(5): Show |
8 | HG00741.hp1 HG02027.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-19765_152-1976 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | ||||||
| chr7:117079968 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.152-19773_152-1976 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | ||||||
| chr7:117079968 | CT | C | 39 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0028 others(36): Show |
39 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.152-19764delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | ||||||
| chr7:117079968 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152-19773_152-1976 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | ||||||
| chr7:117079968 | CTTTTTTT others(9): Show |
C | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-19779_152-1976 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117079968 | ||||||
| chr7:117080019 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(12): Show |
15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-19743C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080019 | |||||||
| chr7:117080129 | C | T | 34 | a0001c0001t0001g0017 a0001c0001t0001g0100 a0001c0001t0001g0102 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.152-19633C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080129 | |||||||
| chr7:117080330 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-19432C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080330 | |||||||
| chr7:117080403 | G | C | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-19359G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080403 | |||||||
| chr7:117080973 | A | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-18789A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080973 | |||||||
| chr7:117080976 | C | T | 12 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.152-18786C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117080976 | |||||||
| chr7:117081135 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-18627T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117081135 | |||||||
| chr7:117081150 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-18612G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117081150 | |||||||
| chr7:117081892 | T | TGA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0109 others(4): Show |
7 | HG02293.hp2 HG02300.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-17850_152-1784 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117081892 | ||||||
| chr7:117081892 | T | TGAGAGA | 26 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
26 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.152-17854_152-1784 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117081892 | ||||||
| chr7:117082104 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152-17658C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082104 | |||||||
| chr7:117082118 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-17644A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082118 | |||||||
| chr7:117082521 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-17241T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082521 | |||||||
| chr7:117082530 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.152-17232T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082530 | |||||||
| chr7:117082532 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0001g0157 |
3 | HG01255.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.152-17230A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082532 | |||||||
| chr7:117082590 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
2 | HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.152-17172C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082590 | |||||||
| chr7:117082635 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.152-17127A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117082635 | |||||||
| chr7:117083116 | A | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(12): Show |
15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-16646A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083116 | |||||||
| chr7:117083162 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-16600C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083162 | |||||||
| chr7:117083167 | C | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0133 others(4): Show |
7 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-16595C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083167 | |||||||
| chr7:117083450 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-16312G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083450 | |||||||
| chr7:117083649 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.152-16113A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083649 | |||||||
| chr7:117083661 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.152-16101T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083661 | |||||||
| chr7:117083829 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-15933T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083829 | |||||||
| chr7:117083842 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.152-15920G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083842 | |||||||
| chr7:117083851 | C | CTG | 31 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(28): Show |
31 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.152-15910_152-1590 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117083851 | ||||||
| chr7:117083992 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-15770G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117083992 | |||||||
| chr7:117084134 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-15628T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084134 | |||||||
| chr7:117084218 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-15544T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084218 | |||||||
| chr7:117084405 | G | C | 27 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-15357G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084405 | |||||||
| chr7:117084689 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(1): Show |
4 | HG00673.hp1 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-15073G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084689 | |||||||
| chr7:117084724 | CATT | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-15028_152-1502 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117084724 | ||||||
| chr7:117084811 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.152-14951T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084811 | |||||||
| chr7:117084893 | T | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0131 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-14869T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117084893 | |||||||
| chr7:117085281 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-14481A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085281 | |||||||
| chr7:117085345 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(1): Show |
4 | HG00673.hp1 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-14417C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085345 | |||||||
| chr7:117085522 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152-14240A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085522 | |||||||
| chr7:117085940 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-13822G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117085940 | |||||||
| chr7:117086778 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0184 |
3 | HG02965.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152-12984C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117086778 | |||||||
| chr7:117087319 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-12443G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117087319 | |||||||
| chr7:117087636 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0104 |
2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.152-12126A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117087636 | |||||||
| chr7:117088047 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-11715C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088047 | |||||||
| chr7:117088238 | T | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0159 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.152-11524T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088238 | |||||||
| chr7:117088442 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.152-11320T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088442 | |||||||
| chr7:117088543 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.152-11219G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088543 | |||||||
| chr7:117088897 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0097 |
3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.152-10865T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088897 | |||||||
| chr7:117088998 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-10764G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117088998 | |||||||
| chr7:117089062 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(11): Show |
14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-10700C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089062 | |||||||
| chr7:117089119 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.152-10643C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089119 | |||||||
| chr7:117089270 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-10492T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089270 | |||||||
| chr7:117089499 | A | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.152-10263A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089499 | |||||||
| chr7:117089566 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152-10196G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089566 | |||||||
| chr7:117089574 | G | GT | 14 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0028 others(11): Show |
14 | HG00738.hp1 HG01255.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-10173dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117089574 | ||||||
| chr7:117089602 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-10160C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089602 | |||||||
| chr7:117089650 | C | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.152-10112C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089650 | |||||||
| chr7:117089657 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.152-10105T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089657 | |||||||
| chr7:117089835 | G | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(8): Show |
11 | HG00673.hp2 HG01943.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-9927G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089835 | |||||||
| chr7:117089904 | AC | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0001g0157 |
3 | HG01255.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.152-9857delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117089904 | |||||||
| chr7:117090236 | A | AAC | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.152-9510_152-9509d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090236 | ||||||
| chr7:117090240 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-9522C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117090240 | |||||||
| chr7:117090254 | GAC | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.152-9485_152-9484d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090254 | ||||||
| chr7:117090254 | GACAC | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.152-9487_152-9484d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090254 | ||||||
| chr7:117090254 | GACACACA others(7): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.152-9497_152-9484d others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117090254 | ||||||
| chr7:117090266 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-9496C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117090266 | |||||||
| chr7:117090413 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-9349G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117090413 | |||||||
| chr7:117091092 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0112 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.152-8670G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117091092 | |||||||
| chr7:117091228 | G | T | 1 | a0001c0001t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.152-8534G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117091228 | |||||||
| chr7:117091334 | G | A | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0132 others(4): Show |
7 | HG00738.hp2 HG01358.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-8428G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117091334 | |||||||
| chr7:117092201 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.152-7561C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117092201 | |||||||
| chr7:117092278 | C | CA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
24 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.152-7458dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | ||||||
| chr7:117092278 | CA | C | 21 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0051 others(18): Show |
21 | HG00323.hp2 HG01433.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.152-7458delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | ||||||
| chr7:117092278 | CAAAAAA | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG00323.hp1 HG02109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-7463_152-7458d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | ||||||
| chr7:117092278 | CAAAAAAA | C | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
22 | HG00408.hp1 HG00673.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.152-7464_152-7458d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092278 | ||||||
| chr7:117092294 | AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0183 |
2 | HG02071.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.152-7457_152-7429d others(31): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092294 | ||||||
| chr7:117092323 | C | CA | 34 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
34 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-7425dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092323 | ||||||
| chr7:117092323 | CA | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0131 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-7425delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117092323 | ||||||
| chr7:117092797 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-6965C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117092797 | |||||||
| chr7:117093152 | G | T | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0131 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-6610G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093152 | |||||||
| chr7:117093478 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.152-6284G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093478 | |||||||
| chr7:117093529 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-6233G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093529 | |||||||
| chr7:117093705 | A | C | 20 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0093 others(17): Show |
20 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.152-6057A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093705 | |||||||
| chr7:117093720 | C | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02027.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.152-6042C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093720 | |||||||
| chr7:117093778 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(11): Show |
14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-5984G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093778 | |||||||
| chr7:117093856 | A | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-5906A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093856 | |||||||
| chr7:117093883 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.152-5879C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117093883 | |||||||
| chr7:117094586 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152-5176C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094586 | |||||||
| chr7:117094677 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-5085C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094677 | |||||||
| chr7:117094935 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-4827G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094935 | |||||||
| chr7:117094942 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0181 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152-4820A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117094942 | |||||||
| chr7:117095138 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-4624A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095138 | |||||||
| chr7:117095540 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.152-4222A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095540 | |||||||
| chr7:117095654 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-4108A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095654 | |||||||
| chr7:117095962 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152-3800G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117095962 | |||||||
| chr7:117096054 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152-3708C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096054 | |||||||
| chr7:117096067 | C | CA | 22 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0028 others(19): Show |
22 | HG00642.hp2 HG00738.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.152-3664dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | ||||||
| chr7:117096067 | C | CAA | 6 | a0001c0001t0001g0055 a0001c0001t0001g0090 a0001c0001t0001g0121 others(3): Show |
6 | HG02257.hp1 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-3665_152-3664d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | ||||||
| chr7:117096067 | CA | C | 38 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(35): Show |
38 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.152-3664delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | ||||||
| chr7:117096067 | CAA | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(26): Show |
29 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.152-3665_152-3664d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | ||||||
| chr7:117096067 | CAAA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0093 others(3): Show |
6 | HG01433.hp1 HG02040.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-3666_152-3664d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | ||||||
| chr7:117096067 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-3674_152-3664d others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | ||||||
| chr7:117096067 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-3675_152-3664d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096067 | ||||||
| chr7:117096178 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.152-3584G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096178 | |||||||
| chr7:117096281 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.152-3481C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096281 | |||||||
| chr7:117096315 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-3447C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096315 | |||||||
| chr7:117096328 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0177 |
3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.152-3434G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096328 | |||||||
| chr7:117096332 | TCTGCCTT others(12): Show |
T | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.152-3427_152-3409d others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117096332 | ||||||
| chr7:117096537 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-3225C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096537 | |||||||
| chr7:117096628 | G | A | 19 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG00738.hp2 HG01358.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-3134G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096628 | |||||||
| chr7:117096734 | G | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0162 |
2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.152-3028G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117096734 | |||||||
| chr7:117097060 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 |
3 | HG02683.hp2 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.152-2702A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097060 | |||||||
| chr7:117097093 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-2669A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097093 | |||||||
| chr7:117097250 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.152-2512C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097250 | |||||||
| chr7:117097326 | G | C | 27 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-2436G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097326 | |||||||
| chr7:117097327 | C | CT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0153 others(2): Show |
5 | HG02293.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-2420dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097327 | ||||||
| chr7:117097422 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-2340T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097422 | |||||||
| chr7:117097599 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0093 others(4): Show |
7 | HG01433.hp1 HG02723.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-2163C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097599 | |||||||
| chr7:117097767 | T | G | 1 | a0001c0001t0001g0007 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.152-1995T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097767 | |||||||
| chr7:117097822 | C | CTA | 42 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(39): Show |
42 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.152-1920_152-1919d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | ||||||
| chr7:117097822 | C | CTATA | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(14): Show |
17 | HG00642.hp1 HG00673.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.152-1922_152-1919d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | ||||||
| chr7:117097822 | C | CTATATA | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.152-1924_152-1919d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | ||||||
| chr7:117097822 | C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152-1928_152-1919d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097822 | ||||||
| chr7:117097880 | C | CTATATA | 4 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG00642.hp1 HG00673.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1858_152-1853d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(1): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0053 others(1): Show |
4 | HG00280.hp2 HG02280.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1860_152-1853d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(3): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0015 others(1): Show |
4 | HG02630.hp2 NA18988.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1862_152-1853d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(5): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0100 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-1864_152-1853d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(7): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0106 others(5): Show |
8 | HG01978.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-1866_152-1853d others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(9): Show |
6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0050 others(3): Show |
6 | HG01358.hp2 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-1868_152-1853d others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(11): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0055 others(4): Show |
7 | HG00642.hp2 HG01978.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-1870_152-1853d others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(13): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0105 others(1): Show |
4 | HG00099.hp1 HG01256.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1872_152-1853d others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(15): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0117 |
2 | HG01081.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.152-1874_152-1853d others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(17): Show |
4 | a0001c0001t0001g0048 a0001c0001t0001g0113 a0001c0001t0001g0120 others(1): Show |
4 | HG00738.hp2 HG02258.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1876_152-1853d others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(19): Show |
1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152-1878_152-1853d others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(21): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0139 |
2 | NA18971.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.152-1880_152-1853d others(30): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | C | CTATATAT others(23): Show |
1 | a0001c0001t0001g0129 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097880 | CTATATAT others(1): Show |
C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0068 others(1): Show |
4 | HG02280.hp1 HG02723.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1860_152-1853d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097880 | ||||||
| chr7:117097884 | A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-1869_152-1868i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097884 | ||||||
| chr7:117097888 | A | ATATATGA others(8): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01433.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-1869_152-1868i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097888 | ||||||
| chr7:117097904 | ATATATTT others(2): Show |
A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0091 others(2): Show |
5 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-1856_152-1848d others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097904 | ||||||
| chr7:117097906 | A | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0080 |
3 | HG00741.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-1856A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097906 | |||||||
| chr7:117097908 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0150 |
2 | NA18981.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0153 a0001c0001t0001g0176 others(1): Show |
4 | HG03041.hp2 HG04184.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1853_152-1852i others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(29): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0177 |
3 | HG00438.hp1 NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0127 |
2 | HG01071.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | HG00099.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0149 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0158 |
3 | HG01934.hp1 HG02071.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0187 |
2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0075 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0109 a0001c0001t0001g0156 a0001c0001t0001g0165 |
3 | HG02965.hp1 NA18747.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0175 |
2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0172 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0182 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(25): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0079 |
2 | HG02523.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0146 |
3 | HG02055.hp1 HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(33): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0084 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.152-1853_152-1852i others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | ATATTTTT others(3): Show |
1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097908 | A | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0080 |
3 | HG00741.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-1854A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097908 | |||||||
| chr7:117097908 | ATTTTTTT | A | 14 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(11): Show |
14 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.152-1840_152-1834d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117097908 | ||||||
| chr7:117097909 | T | TATATATA | 2 | a0001c0001t0001g0041 a0001c0001t0001g0188 |
2 | HG01943.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097909 | T | TATATATA others(2): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0181 |
3 | HG02040.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097909 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097909 | T | TATATATA others(6): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01943.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097909 | T | TATATATA others(8): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0110 a0001c0001t0001g0160 |
3 | HG00323.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.152-1853_152-1852i others(17): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097909 | T | TATATATA others(10): Show |
4 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0065 others(1): Show |
4 | HG02647.hp1 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1853_152-1852i others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097909 | T | TATATATA others(12): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0073 others(1): Show |
4 | HG01081.hp2 HG01496.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1853_152-1852i others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097909 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.152-1853_152-1852i others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097909 | |||||||
| chr7:117097910 | T | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(41): Show |
44 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.152-1852T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097910 | |||||||
| chr7:117097911 | T | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(14): Show |
17 | HG00323.hp2 HG01081.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-1851T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097911 | |||||||
| chr7:117097912 | T | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(13): Show |
16 | HG00099.hp1 HG00280.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.152-1850T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097912 | |||||||
| chr7:117097913 | T | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0049 others(1): Show |
4 | HG01081.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1849T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097913 | |||||||
| chr7:117097914 | T | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0102 others(1): Show |
4 | HG00280.hp2 HG01978.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1848T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097914 | |||||||
| chr7:117097915 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0022 |
2 | HG02257.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.152-1847T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097915 | |||||||
| chr7:117097916 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152-1846T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097916 | |||||||
| chr7:117097917 | T | A | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.152-1845T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097917 | |||||||
| chr7:117097970 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152-1792C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117097970 | |||||||
| chr7:117098008 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0070 |
2 | HG01433.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.152-1754C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098008 | |||||||
| chr7:117098102 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-1660G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098102 | |||||||
| chr7:117098186 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01071.hp1 HG01255.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.152-1576G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098186 | |||||||
| chr7:117098524 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152-1238G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098524 | |||||||
| chr7:117098534 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.152-1228T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098534 | |||||||
| chr7:117098589 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.152-1173A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098589 | |||||||
| chr7:117098765 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0032 |
2 | HG02071.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.152-997T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117098765 | |||||||
| chr7:117099046 | C | CA | 20 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0099 others(17): Show |
20 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-697dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAA | 11 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0057 others(8): Show |
11 | HG01192.hp1 HG01358.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-698_152-697dup others(2): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAA | 32 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0043 others(29): Show |
32 | HG00438.hp1 HG01255.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.152-699_152-697dup others(3): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAA | 11 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0091 others(8): Show |
11 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-700_152-697dup others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAA | 18 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
18 | HG00408.hp1 HG01192.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-701_152-697dup others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0037 others(3): Show |
6 | HG00673.hp1 HG01071.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-703_152-697dup others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0145 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.152-707_152-697dup others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.152-709_152-697dup others(13): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0142 |
3 | HG02717.hp2 HG02895.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.152-710_152-697dup others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152-711_152-697dup others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0131 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.152-714_152-697dup others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.152-715_152-697dup others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099046 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0141 |
3 | HG00408.hp2 HG02523.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.152-697_152-696ins others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099046 | ||||||
| chr7:117099052 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152-699_152-686del others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099052 | ||||||
| chr7:117099055 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.152-696_152-686del others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099055 | ||||||
| chr7:117099063 | AAAC | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(4): Show |
7 | HG02055.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-696_152-694del others(3): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr7 | 117099063 | ||||||
| chr7:117099065 | AC | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
23 | HG00099.hp2 HG00642.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-696delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099065 | |||||||
| chr7:117099066 | C | A | 136 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.152-696C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099066 | |||||||
| chr7:117099081 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-681A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099081 | |||||||
| chr7:117099315 | T | G | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0131 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.152-447T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099315 | |||||||
| chr7:117099448 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152-314A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099448 | |||||||
| chr7:117099571 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152-191A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099571 | |||||||
| chr7:117099650 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(2): Show |
5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-112A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 1/15 | chr7 | 117099650 | |||||||
| chr7:117100284 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+440C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117100284 | |||||||
| chr7:117100606 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+762T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117100606 | |||||||
| chr7:117100758 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+914G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117100758 | |||||||
| chr7:117101025 | G | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+1181G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101025 | |||||||
| chr7:117101174 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+1330G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101174 | |||||||
| chr7:117101492 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234+1648T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101492 | |||||||
| chr7:117101541 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+1697A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117101541 | |||||||
| chr7:117102033 | T | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(12): Show |
15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+2189T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102033 | |||||||
| chr7:117102302 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0112 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.234+2458C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102302 | |||||||
| chr7:117102376 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.234+2532G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102376 | |||||||
| chr7:117102393 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0108 |
2 | NA20805.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.234+2549A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102393 | |||||||
| chr7:117102482 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.234+2638C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102482 | |||||||
| chr7:117102944 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.234+3100T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117102944 | |||||||
| chr7:117103243 | G | GA | 6 | a0001c0001t0001g0125 a0001c0001t0001g0139 a0001c0001t0001g0149 others(3): Show |
6 | HG02258.hp1 NA18965.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+3408dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117103243 | ||||||
| chr7:117103293 | A | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+3449A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117103293 | |||||||
| chr7:117103325 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.234+3481A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117103325 | |||||||
| chr7:117103621 | TCTAAGA | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+3779_234+3784d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117103621 | ||||||
| chr7:117103746 | T | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0131 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+3902T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117103746 | |||||||
| chr7:117104113 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.234+4269G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104113 | |||||||
| chr7:117104372 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0181 |
2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.234+4528G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104372 | |||||||
| chr7:117104463 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.234+4619T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104463 | |||||||
| chr7:117104555 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.234+4711C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104555 | |||||||
| chr7:117104623 | T | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(11): Show |
14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+4779T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104623 | |||||||
| chr7:117104686 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4842G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104686 | |||||||
| chr7:117104793 | T | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+4949T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117104793 | |||||||
| chr7:117105009 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.234+5165C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105009 | |||||||
| chr7:117105036 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5192T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105036 | |||||||
| chr7:117105175 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.234+5331G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105175 | |||||||
| chr7:117105427 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0093 others(4): Show |
7 | HG01433.hp1 HG02723.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+5583C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105427 | |||||||
| chr7:117105499 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5655G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105499 | |||||||
| chr7:117105505 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5661T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105505 | |||||||
| chr7:117105726 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+5882A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105726 | |||||||
| chr7:117105925 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 |
3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6081G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105925 | |||||||
| chr7:117105988 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.234+6144T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117105988 | |||||||
| chr7:117105998 | G | GT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(3): Show |
6 | HG02083.hp1 HG03098.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+6165dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117105998 | ||||||
| chr7:117105998 | GT | G | 57 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(54): Show |
57 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.234+6165delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117105998 | ||||||
| chr7:117106004 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.234+6160T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106004 | |||||||
| chr7:117106005 | T | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.234+6161T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106005 | |||||||
| chr7:117106046 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.234+6202C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106046 | |||||||
| chr7:117106047 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0151 a0001c0001t0001g0156 others(2): Show |
5 | HG02027.hp1 HG02083.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+6203G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106047 | |||||||
| chr7:117106150 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
82 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.234+6306C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106150 | |||||||
| chr7:117106159 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6315G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106159 | |||||||
| chr7:117106183 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+6339A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106183 | |||||||
| chr7:117106261 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.234+6417G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106261 | |||||||
| chr7:117106409 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.234+6565A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106409 | |||||||
| chr7:117106454 | T | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6610T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106454 | |||||||
| chr7:117106616 | C | CT | 7 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0100 others(4): Show |
7 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+6794dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117106616 | ||||||
| chr7:117106616 | CT | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0068 others(7): Show |
10 | HG01433.hp2 HG01496.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.234+6794delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117106616 | ||||||
| chr7:117106651 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+6807T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106651 | |||||||
| chr7:117106781 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+6937C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106781 | |||||||
| chr7:117106810 | C | T | 28 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
28 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.234+6966C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106810 | |||||||
| chr7:117106893 | T | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.234+7049T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117106893 | |||||||
| chr7:117107123 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+7279A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107123 | |||||||
| chr7:117107206 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+7362G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107206 | |||||||
| chr7:117107603 | C | CT | 21 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0033 others(18): Show |
21 | HG00099.hp1 HG00741.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+7785dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117107603 | ||||||
| chr7:117107603 | CT | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0058 others(22): Show |
25 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.234+7785delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117107603 | ||||||
| chr7:117107867 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.234+8023G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107867 | |||||||
| chr7:117107944 | C | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.234+8100C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117107944 | |||||||
| chr7:117108276 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.234+8432C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117108276 | |||||||
| chr7:117108843 | T | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.234+8999T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117108843 | |||||||
| chr7:117109196 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.234+9352A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109196 | |||||||
| chr7:117109217 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.234+9373T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109217 | |||||||
| chr7:117109330 | GAGA | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+9493_234+9495d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117109330 | ||||||
| chr7:117109369 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.234+9525C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109369 | |||||||
| chr7:117109461 | T | TAGA | 2 | a0001c0001t0001g0085 a0001c0001t0001g0166 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.234+9621_234+9623d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117109461 | ||||||
| chr7:117109475 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+9631G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109475 | |||||||
| chr7:117109673 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.234+9829C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109673 | |||||||
| chr7:117109767 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.235-9794A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109767 | |||||||
| chr7:117109773 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-9788G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117109773 | |||||||
| chr7:117110156 | G | C | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.235-9405G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110156 | |||||||
| chr7:117110255 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0001g0157 |
3 | HG01255.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.235-9306G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110255 | |||||||
| chr7:117110440 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-9121G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110440 | |||||||
| chr7:117110649 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.235-8912G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117110649 | |||||||
| chr7:117111072 | GAGCTTGT others(10): Show |
G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.235-8485_235-8469d others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117111072 | ||||||
| chr7:117111190 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0081 |
2 | NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.235-8371C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111190 | |||||||
| chr7:117111569 | G | A | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0093 others(4): Show |
7 | HG01433.hp1 HG02723.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-7992G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111569 | |||||||
| chr7:117111821 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 |
3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7740T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111821 | |||||||
| chr7:117111860 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7701G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111860 | |||||||
| chr7:117111863 | G | GT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(12): Show |
15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.235-7697dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117111863 | ||||||
| chr7:117111943 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-7618T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117111943 | |||||||
| chr7:117112108 | G | GTGTGTGT others(17): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7452_235-7451i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117112108 | ||||||
| chr7:117112119 | T | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-7442T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112119 | |||||||
| chr7:117112129 | G | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(4): Show |
7 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-7432G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112129 | |||||||
| chr7:117112238 | A | G | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(4): Show |
7 | HG01433.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-7323A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112238 | |||||||
| chr7:117112365 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.235-7196A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112365 | |||||||
| chr7:117112612 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.235-6949C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112612 | |||||||
| chr7:117112633 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0112 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.235-6928G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117112633 | |||||||
| chr7:117113042 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.235-6519G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113042 | |||||||
| chr7:117113297 | T | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-6264T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113297 | |||||||
| chr7:117113444 | GAA | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(2): Show |
5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-6115_235-6114d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr7 | 117113444 | ||||||
| chr7:117113451 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-6110A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113451 | |||||||
| chr7:117113766 | G | T | 20 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0093 others(17): Show |
20 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.235-5795G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117113766 | |||||||
| chr7:117114099 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235-5462A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114099 | |||||||
| chr7:117114340 | G | A | 20 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0093 others(17): Show |
20 | HG00408.hp2 HG00438.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.235-5221G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114340 | |||||||
| chr7:117114634 | G | A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.235-4927G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114634 | |||||||
| chr7:117114808 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(11): Show |
14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.235-4753A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114808 | |||||||
| chr7:117114921 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.235-4640G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114921 | |||||||
| chr7:117114931 | G | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-4630G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117114931 | |||||||
| chr7:117115058 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.235-4503C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115058 | |||||||
| chr7:117115281 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.235-4280A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115281 | |||||||
| chr7:117115474 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.235-4087C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115474 | |||||||
| chr7:117115624 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-3937G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117115624 | |||||||
| chr7:117116469 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.235-3092G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116469 | |||||||
| chr7:117116481 | C | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-3080C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116481 | |||||||
| chr7:117116695 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(2): Show |
5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2866C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116695 | |||||||
| chr7:117116773 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.235-2788C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116773 | |||||||
| chr7:117116782 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-2779A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116782 | |||||||
| chr7:117116842 | A | G | 5 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0167 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-2719A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117116842 | |||||||
| chr7:117117079 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-2482G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117079 | |||||||
| chr7:117117342 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0020 |
3 | HG00642.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.235-2219G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117342 | |||||||
| chr7:117117400 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.235-2161T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117400 | |||||||
| chr7:117117473 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.235-2088A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117473 | |||||||
| chr7:117117505 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-2056A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117505 | |||||||
| chr7:117117702 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-1859G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117702 | |||||||
| chr7:117117790 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG00673.hp2 HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.235-1771G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117790 | |||||||
| chr7:117117805 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.235-1756C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117805 | |||||||
| chr7:117117937 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.235-1624T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117117937 | |||||||
| chr7:117118003 | C | T | 27 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.235-1558C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118003 | |||||||
| chr7:117118116 | A | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0167 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-1445A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118116 | |||||||
| chr7:117118613 | T | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0131 others(10): Show |
13 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-948T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118613 | |||||||
| chr7:117118707 | G | A | 58 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(55): Show |
58 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.235-854G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117118707 | |||||||
| chr7:117119109 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.235-452G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117119109 | |||||||
| chr7:117119280 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.235-281T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117119280 | |||||||
| chr7:117119361 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.235-200C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 2/15 | chr7 | 117119361 | |||||||
| chr7:117119796 | T | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+76T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117119796 | |||||||
| chr7:117119880 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0112 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.394+160G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117119880 | |||||||
| chr7:117119935 | C | CT | 36 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(33): Show |
36 | HG00323.hp2 HG00438.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.394+226dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117119935 | ||||||
| chr7:117120006 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.394+286G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120006 | |||||||
| chr7:117120411 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+691G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120411 | |||||||
| chr7:117120478 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.394+758G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120478 | |||||||
| chr7:117120586 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.394+866C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120586 | |||||||
| chr7:117120981 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394+1261G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117120981 | |||||||
| chr7:117121589 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+1869A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121589 | |||||||
| chr7:117121659 | A | G | 15 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(12): Show |
15 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.394+1939A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121659 | |||||||
| chr7:117121782 | A | G | 6 | a0001c0001t0001g0123 a0001c0001t0001g0132 a0001c0001t0001g0136 others(3): Show |
6 | HG00738.hp2 HG01358.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.394+2062A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121782 | |||||||
| chr7:117121887 | T | TAAGAGGA others(263): Show |
1 | a0001c0001t0001g0038 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.394+2176_394+2177i others(272): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | ||||||
| chr7:117121887 | T | TAAGAGGA others(269): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01943.hp1 HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.394+2176_394+2177i others(278): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | ||||||
| chr7:117121887 | T | TAAGAGGA others(270): Show |
1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.394+2176_394+2177i others(279): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | ||||||
| chr7:117121887 | T | TAAGAGGA others(271): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(2): Show |
5 | HG02040.hp2 HG02273.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+2176_394+2177i others(280): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | ||||||
| chr7:117121887 | T | TAAGAGGA others(276): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0039 |
2 | NA18990.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.394+2176_394+2177i others(285): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | ||||||
| chr7:117121887 | T | TAAGAGGA others(277): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0020 |
2 | HG00642.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.394+2176_394+2177i others(286): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117121887 | ||||||
| chr7:117121992 | T | C | 18 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(15): Show |
18 | HG00738.hp2 HG01358.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.394+2272T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117121992 | |||||||
| chr7:117122098 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+2378T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122098 | |||||||
| chr7:117122246 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.394+2526A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122246 | |||||||
| chr7:117122267 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.394+2547T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122267 | |||||||
| chr7:117122355 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.394+2635G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122355 | |||||||
| chr7:117122536 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+2816A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122536 | |||||||
| chr7:117122858 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.394+3138G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117122858 | |||||||
| chr7:117123206 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.394+3486G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123206 | |||||||
| chr7:117123282 | A | G | 27 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.394+3562A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123282 | |||||||
| chr7:117123522 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.394+3802G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123522 | |||||||
| chr7:117123891 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.394+4171A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123891 | |||||||
| chr7:117123983 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.394+4263A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117123983 | |||||||
| chr7:117124036 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.394+4316A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117124036 | |||||||
| chr7:117124129 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0167 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+4409C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117124129 | |||||||
| chr7:117124295 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(12): Show |
15 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.394+4575C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117124295 | |||||||
| chr7:117125045 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-4748T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117125045 | |||||||
| chr7:117125215 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.395-4578C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117125215 | |||||||
| chr7:117125225 | G | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.395-4568G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117125225 | |||||||
| chr7:117126261 | C | CT | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-3524dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr7 | 117126261 | ||||||
| chr7:117126835 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.395-2958T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126835 | |||||||
| chr7:117126863 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.395-2930C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126863 | |||||||
| chr7:117126867 | G | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG02818.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.395-2926G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126867 | |||||||
| chr7:117126981 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-2812A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126981 | |||||||
| chr7:117126996 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395-2797G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117126996 | |||||||
| chr7:117127500 | T | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-2293T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117127500 | |||||||
| chr7:117127910 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.395-1883G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117127910 | |||||||
| chr7:117128161 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 |
3 | HG02109.hp2 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-1632G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128161 | |||||||
| chr7:117128341 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.395-1452C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128341 | |||||||
| chr7:117128533 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-1260T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128533 | |||||||
| chr7:117128820 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02257.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.395-973A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128820 | |||||||
| chr7:117128898 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.395-895G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117128898 | |||||||
| chr7:117129168 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.395-625A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117129168 | |||||||
| chr7:117129448 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.395-345C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117129448 | |||||||
| chr7:117129516 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.395-277A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 3/15 | chr7 | 117129516 | |||||||
| chr7:117130351 | A | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.450-140A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 4/15 | chr7 | 117130351 | |||||||
| chr7:117130661 | A | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(12): Show |
15 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+55A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 5/15 | chr7 | 117130661 | |||||||
| chr7:117132075 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.641+115G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132075 | |||||||
| chr7:117132252 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.641+292T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132252 | |||||||
| chr7:117132273 | A | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0129 |
2 | HG01358.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.641+313A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132273 | |||||||
| chr7:117132343 | A | G | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG00438.hp2 HG02040.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+383A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132343 | |||||||
| chr7:117132798 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.641+838C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117132798 | |||||||
| chr7:117133089 | A | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.642-1035A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133089 | |||||||
| chr7:117133106 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.642-1018C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133106 | |||||||
| chr7:117133180 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.642-944G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133180 | |||||||
| chr7:117133650 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(2): Show |
5 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-474G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133650 | |||||||
| chr7:117133791 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.642-333C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133791 | |||||||
| chr7:117133835 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.642-289G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133835 | |||||||
| chr7:117133910 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.642-214T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 6/15 | chr7 | 117133910 | |||||||
| chr7:117134208 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.710+16G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134208 | |||||||
| chr7:117134447 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.710+255G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134447 | |||||||
| chr7:117134447 | G | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.710+255G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134447 | |||||||
| chr7:117134959 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.710+767C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134959 | |||||||
| chr7:117134992 | A | T | 17 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+800A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134992 | |||||||
| chr7:117134993 | T | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0072 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+801T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117134993 | |||||||
| chr7:117135546 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.711-535T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117135546 | |||||||
| chr7:117135593 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.711-488A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117135593 | |||||||
| chr7:117136047 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.711-34T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 7/15 | chr7 | 117136047 | |||||||
| chr7:117136386 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.865+151A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136386 | |||||||
| chr7:117136543 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.865+308G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136543 | |||||||
| chr7:117136562 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.865+327T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136562 | |||||||
| chr7:117136672 | T | C | 25 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0051 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.865+437T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136672 | |||||||
| chr7:117136817 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.865+582A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136817 | |||||||
| chr7:117136947 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.865+712G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117136947 | |||||||
| chr7:117137268 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.865+1033C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137268 | |||||||
| chr7:117137441 | A | G | 5 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0167 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.866-994A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137441 | |||||||
| chr7:117137448 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.866-987A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137448 | |||||||
| chr7:117137577 | A | G | 27 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.866-858A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137577 | |||||||
| chr7:117137755 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.866-680T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137755 | |||||||
| chr7:117137852 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.866-583A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137852 | |||||||
| chr7:117137853 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.866-582C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137853 | |||||||
| chr7:117137868 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.866-567A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117137868 | |||||||
| chr7:117138385 | C | T | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 others(1): Show |
4 | NA18965.hp2 NA18971.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-50C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117138385 | |||||||
| chr7:117138404 | A | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG00408.hp1 HG01192.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-31A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 8/15 | chr7 | 117138404 | |||||||
| chr7:117138704 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0176 |
2 | HG00323.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.963+172A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117138704 | |||||||
| chr7:117138792 | T | G | 25 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(22): Show |
25 | HG00408.hp2 HG00438.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.963+260T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117138792 | |||||||
| chr7:117139021 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(11): Show |
14 | HG00642.hp1 HG00673.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.963+489A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139021 | |||||||
| chr7:117139540 | C | T | 47 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(44): Show |
47 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.963+1008C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139540 | |||||||
| chr7:117139631 | A | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+1099A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139631 | |||||||
| chr7:117139914 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+1382G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139914 | |||||||
| chr7:117139992 | C | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0104 |
2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.963+1460C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117139992 | |||||||
| chr7:117140055 | T | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0160 a0001c0001t0001g0162 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+1523T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140055 | |||||||
| chr7:117140129 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+1597A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140129 | |||||||
| chr7:117140134 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0085 a0001c0001t0001g0125 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1602A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140134 | |||||||
| chr7:117140329 | T | C | 12 | a0001c0001t0001g0053 a0001c0001t0001g0088 a0001c0001t0001g0090 others(9): Show |
12 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+1797T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140329 | |||||||
| chr7:117140445 | A | G | 35 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0047 others(32): Show |
35 | HG01433.hp1 HG01496.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.963+1913A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140445 | |||||||
| chr7:117140520 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.963+1988G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140520 | |||||||
| chr7:117140564 | A | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+2032A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140564 | |||||||
| chr7:117140572 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0092 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.963+2040C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140572 | |||||||
| chr7:117140686 | A | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0088 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+2154A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140686 | |||||||
| chr7:117140801 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+2269G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140801 | |||||||
| chr7:117140813 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.963+2281T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140813 | |||||||
| chr7:117140882 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.963+2350A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140882 | |||||||
| chr7:117140912 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(14): Show |
17 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+2380A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117140912 | |||||||
| chr7:117141076 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0116 |
2 | HG00280.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.963+2544G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141076 | |||||||
| chr7:117141112 | A | T | 1 | a0001c0001t0001g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.963+2580A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141112 | |||||||
| chr7:117141190 | C | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+2658C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141190 | |||||||
| chr7:117141224 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+2692C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141224 | |||||||
| chr7:117141381 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+2849G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141381 | |||||||
| chr7:117141503 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.963+2971G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141503 | |||||||
| chr7:117141748 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+3216C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141748 | |||||||
| chr7:117141809 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(10): Show |
13 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.963+3277G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141809 | |||||||
| chr7:117141815 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+3283G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141815 | |||||||
| chr7:117141858 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0188 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+3326C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141858 | |||||||
| chr7:117141921 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+3389C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117141921 | |||||||
| chr7:117142172 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+3640G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142172 | |||||||
| chr7:117142293 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+3761A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142293 | |||||||
| chr7:117142352 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+3820C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142352 | |||||||
| chr7:117142381 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.963+3849T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142381 | |||||||
| chr7:117142427 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.963+3895G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142427 | |||||||
| chr7:117142481 | GA | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+3959delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117142481 | ||||||
| chr7:117142811 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+4279C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142811 | |||||||
| chr7:117142847 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.963+4315T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142847 | |||||||
| chr7:117142862 | G | A | 14 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.963+4330G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142862 | |||||||
| chr7:117142935 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+4403T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117142935 | |||||||
| chr7:117143429 | C | A | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0133 others(5): Show |
8 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+4897C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143429 | |||||||
| chr7:117143593 | C | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0001g0142 others(1): Show |
4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+5061C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143593 | |||||||
| chr7:117143621 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+5089C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143621 | |||||||
| chr7:117143962 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+5430A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117143962 | |||||||
| chr7:117144401 | G | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0001g0142 others(1): Show |
4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+5869G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144401 | |||||||
| chr7:117144523 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+5991C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144523 | |||||||
| chr7:117144584 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
74 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.963+6052A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144584 | |||||||
| chr7:117144633 | C | CA | 49 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.963+6117dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117144633 | ||||||
| chr7:117144633 | C | CAAA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(14): Show |
17 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.963+6115_963+6117d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117144633 | ||||||
| chr7:117144691 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.963+6159C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144691 | |||||||
| chr7:117144850 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+6318A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144850 | |||||||
| chr7:117144853 | T | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0001g0142 others(1): Show |
4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+6321T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117144853 | |||||||
| chr7:117145014 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+6482A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145014 | |||||||
| chr7:117145057 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
14 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.963+6525A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145057 | |||||||
| chr7:117145113 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.963+6581A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145113 | |||||||
| chr7:117145157 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+6625A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145157 | |||||||
| chr7:117145204 | CA | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.963+6681delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117145204 | ||||||
| chr7:117145234 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0188 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+6702A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145234 | |||||||
| chr7:117145320 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
14 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.963+6788A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145320 | |||||||
| chr7:117145524 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+6992T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145524 | |||||||
| chr7:117145633 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+7101G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145633 | |||||||
| chr7:117145973 | C | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.963+7441C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117145973 | |||||||
| chr7:117146068 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.963+7536A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146068 | |||||||
| chr7:117146133 | A | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+7601A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146133 | |||||||
| chr7:117146369 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.963+7837G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146369 | |||||||
| chr7:117146491 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.963+7959A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146491 | |||||||
| chr7:117146580 | G | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+8048G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146580 | |||||||
| chr7:117146696 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.963+8164G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117146696 | |||||||
| chr7:117147122 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+8590A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147122 | |||||||
| chr7:117147280 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+8748G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147280 | |||||||
| chr7:117147382 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+8850C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147382 | |||||||
| chr7:117147455 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+8923C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147455 | |||||||
| chr7:117147755 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+9223C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147755 | |||||||
| chr7:117147890 | AAGCATAC | A | 11 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+9360_963+9366d others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117147890 | ||||||
| chr7:117147899 | T | A | 11 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+9367T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147899 | |||||||
| chr7:117147991 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+9459G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117147991 | |||||||
| chr7:117148031 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+9499T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148031 | |||||||
| chr7:117148153 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+9621C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148153 | |||||||
| chr7:117148231 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.963+9699A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148231 | |||||||
| chr7:117148363 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+9831T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148363 | |||||||
| chr7:117148386 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+9854A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148386 | |||||||
| chr7:117148675 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.963+10143G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148675 | |||||||
| chr7:117148756 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.963+10224G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148756 | |||||||
| chr7:117148994 | T | C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+10462T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117148994 | |||||||
| chr7:117149173 | C | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+10641C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149173 | |||||||
| chr7:117149217 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+10685A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149217 | |||||||
| chr7:117149222 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0188 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+10690G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149222 | |||||||
| chr7:117149302 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+10770A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149302 | |||||||
| chr7:117149461 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.963+10929A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149461 | |||||||
| chr7:117149592 | C | CT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0082 others(9): Show |
12 | HG00280.hp2 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+11083dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | ||||||
| chr7:117149592 | CT | C | 23 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0051 others(20): Show |
23 | HG01433.hp2 HG01496.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.963+11083delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | ||||||
| chr7:117149592 | CTT | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0046 others(8): Show |
11 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+11082_963+1108 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | ||||||
| chr7:117149592 | CTTT | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(37): Show |
40 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(37): Show |
intron_variant | MODIFIER | c.963+11081_963+1108 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | ||||||
| chr7:117149592 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.963+11073_963+1108 others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117149592 | ||||||
| chr7:117149714 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.963+11182C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149714 | |||||||
| chr7:117149880 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
69 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.963+11348G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149880 | |||||||
| chr7:117149889 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.963+11357G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149889 | |||||||
| chr7:117149918 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.963+11386A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149918 | |||||||
| chr7:117149975 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0118 |
2 | HG03492.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.963+11443G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117149975 | |||||||
| chr7:117150138 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+11606C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150138 | |||||||
| chr7:117150205 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(14): Show |
17 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.963+11673G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150205 | |||||||
| chr7:117150439 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.963+11907G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150439 | |||||||
| chr7:117150558 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+12026C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117150558 | |||||||
| chr7:117151048 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+12516G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151048 | |||||||
| chr7:117151085 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0105 |
2 | HG00099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.963+12553G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151085 | |||||||
| chr7:117151117 | G | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+12585G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151117 | |||||||
| chr7:117151470 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.963+12938A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151470 | |||||||
| chr7:117151530 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+12998T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151530 | |||||||
| chr7:117151544 | A | AT | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+13019dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117151544 | ||||||
| chr7:117151706 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.963+13174A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151706 | |||||||
| chr7:117151717 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+13185T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151717 | |||||||
| chr7:117151839 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+13307G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117151839 | |||||||
| chr7:117152083 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0166 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.963+13551C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152083 | |||||||
| chr7:117152118 | C | CAA | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(49): Show |
52 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.963+13594_963+1359 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152118 | ||||||
| chr7:117152128 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0059 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.963+13596T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152128 | |||||||
| chr7:117152162 | TTATATAT others(12): Show |
T | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.963+13641_963+1365 others(23): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152162 | ||||||
| chr7:117152173 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.963+13641A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152173 | |||||||
| chr7:117152177 | C | CTA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG00099.hp1 HG01071.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.963+13690_963+1369 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | C | CTATA | 12 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0025 others(9): Show |
12 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+13688_963+1369 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | C | CTATATA | 4 | a0001c0001t0001g0030 a0001c0001t0001g0078 a0001c0001t0001g0110 others(1): Show |
4 | HG00323.hp2 HG00408.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+13686_963+1369 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | C | CTATATAT others(1): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0077 others(3): Show |
6 | HG00673.hp1 HG01071.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+13684_963+1369 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0144 |
2 | NA18747.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.963+13682_963+1369 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTA | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0032 others(7): Show |
10 | HG01081.hp2 HG01358.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+13690_963+1369 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATA | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0080 others(1): Show |
4 | HG00741.hp1 HG01255.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+13688_963+1369 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATA | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0136 a0001c0001t0001g0156 |
3 | HG00738.hp2 HG02965.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.963+13686_963+1369 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0166 |
3 | HG02451.hp2 HG02976.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.963+13684_963+1369 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(3): Show |
C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0153 a0001c0001t0001g0159 |
3 | HG02683.hp2 NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.963+13682_963+1369 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(5): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.963+13680_963+1369 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.963+13676_963+1369 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(11): Show |
C | 11 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(8): Show |
11 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+13674_963+1369 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(21): Show |
C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(10): Show |
13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.963+13664_963+1369 others(32): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(25): Show |
C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+13660_963+1369 others(36): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(27): Show |
C | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.963+13658_963+1369 others(38): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152177 | CTATATAT others(29): Show |
C | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.963+13656_963+1369 others(40): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152177 | ||||||
| chr7:117152184 | TATA | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+13653_963+1365 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152184 | |||||||
| chr7:117152184 | TATATATA others(8): Show |
T | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.963+13653_963+1366 others(19): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152184 | |||||||
| chr7:117152184 | TATATATA others(10): Show |
T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.963+13653_963+1366 others(21): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152184 | |||||||
| chr7:117152185 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.963+13653A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152185 | |||||||
| chr7:117152189 | A | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.963+13657A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152189 | |||||||
| chr7:117152202 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.963+13683_963+1368 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117152202 | ||||||
| chr7:117152203 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.963+13671A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152203 | |||||||
| chr7:117152222 | T | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
53 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.963+13690T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152222 | |||||||
| chr7:117152250 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.963+13718G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152250 | |||||||
| chr7:117152283 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.963+13751A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152283 | |||||||
| chr7:117152754 | A | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+14222A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152754 | |||||||
| chr7:117152771 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.963+14239G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152771 | |||||||
| chr7:117152859 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+14327T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152859 | |||||||
| chr7:117152949 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0188 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+14417C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117152949 | |||||||
| chr7:117153033 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+14501A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153033 | |||||||
| chr7:117153374 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.963+14842T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153374 | |||||||
| chr7:117153376 | G | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0001g0142 others(1): Show |
4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+14844G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153376 | |||||||
| chr7:117153388 | A | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0001g0142 others(1): Show |
4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+14856A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153388 | |||||||
| chr7:117153456 | A | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0001g0142 others(1): Show |
4 | HG02895.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+14924A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153456 | |||||||
| chr7:117153546 | T | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0087 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.963+15014T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153546 | |||||||
| chr7:117153694 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.963+15162A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117153694 | |||||||
| chr7:117154068 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.963+15536C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154068 | |||||||
| chr7:117154230 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.963+15698G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154230 | |||||||
| chr7:117154380 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.963+15848A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154380 | |||||||
| chr7:117154941 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964-15921A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117154941 | |||||||
| chr7:117155576 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-15286G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117155576 | |||||||
| chr7:117155804 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-15058A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117155804 | |||||||
| chr7:117155815 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.964-15047A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117155815 | |||||||
| chr7:117156029 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.964-14833A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156029 | |||||||
| chr7:117156050 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-14812C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156050 | |||||||
| chr7:117156094 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0188 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-14768A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156094 | |||||||
| chr7:117156222 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0142 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-14640C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156222 | |||||||
| chr7:117156442 | T | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-14420T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156442 | |||||||
| chr7:117156584 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-14278A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156584 | |||||||
| chr7:117156599 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0112 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-14263T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156599 | |||||||
| chr7:117156904 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.964-13958T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156904 | |||||||
| chr7:117156955 | A | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-13907A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117156955 | |||||||
| chr7:117157025 | C | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-13837C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157025 | |||||||
| chr7:117157085 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-13777A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157085 | |||||||
| chr7:117157216 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-13646T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157216 | |||||||
| chr7:117157625 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.964-13237A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157625 | |||||||
| chr7:117157888 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0138 |
3 | NA19000.hp2 NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.964-12974C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157888 | |||||||
| chr7:117157985 | A | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(1): Show |
4 | HG00673.hp1 HG01071.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-12877A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117157985 | |||||||
| chr7:117158372 | A | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-12490A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117158372 | |||||||
| chr7:117158659 | A | G | 13 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(10): Show |
13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-12203A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117158659 | |||||||
| chr7:117158835 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.964-12027C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117158835 | |||||||
| chr7:117159118 | G | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11744G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159118 | |||||||
| chr7:117159352 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.964-11510C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159352 | |||||||
| chr7:117159358 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0062 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-11504T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159358 | |||||||
| chr7:117159386 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11476C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159386 | |||||||
| chr7:117159396 | A | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11466A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159396 | |||||||
| chr7:117159399 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.964-11463G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159399 | |||||||
| chr7:117159412 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-11450T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159412 | |||||||
| chr7:117159521 | A | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-11341A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159521 | |||||||
| chr7:117159533 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(49): Show |
52 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.964-11329T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159533 | |||||||
| chr7:117159582 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.964-11280A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159582 | |||||||
| chr7:117159635 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.964-11227G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159635 | |||||||
| chr7:117159815 | C | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.964-11047C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159815 | |||||||
| chr7:117159871 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-10991C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159871 | |||||||
| chr7:117159872 | G | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0156 others(4): Show |
7 | HG00438.hp1 HG00642.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-10990G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159872 | |||||||
| chr7:117159929 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-10933C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159929 | |||||||
| chr7:117159958 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.964-10904T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117159958 | |||||||
| chr7:117160043 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0188 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-10819A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160043 | |||||||
| chr7:117160182 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-10680A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160182 | |||||||
| chr7:117160243 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-10619A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160243 | |||||||
| chr7:117160246 | AG | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(42): Show |
45 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.964-10615delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160246 | |||||||
| chr7:117160284 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.964-10578A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160284 | |||||||
| chr7:117160542 | ATC | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-10308_964-1030 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160542 | ||||||
| chr7:117160618 | A | G | 11 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.964-10244A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160618 | |||||||
| chr7:117160653 | G | GTA | 2 | a0001c0001t0001g0058 a0001c0001t0001g0064 |
2 | HG01496.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.964-10194_964-1019 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | ||||||
| chr7:117160653 | G | GTGTATAT others(3): Show |
33 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(30): Show |
33 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.964-10208_964-1020 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | ||||||
| chr7:117160653 | G | GTGTATAT others(5): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0023 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.964-10208_964-1020 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | ||||||
| chr7:117160653 | G | GTGTATAT others(7): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0162 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.964-10208_964-1020 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117160653 | ||||||
| chr7:117160655 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.964-10207A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160655 | |||||||
| chr7:117160661 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964-10201A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117160661 | |||||||
| chr7:117161075 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.964-9787A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161075 | |||||||
| chr7:117161090 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-9772G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161090 | |||||||
| chr7:117161100 | GT | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(33): Show |
36 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.964-9749delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161100 | ||||||
| chr7:117161100 | GTT | G | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0062 others(9): Show |
12 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.964-9750_964-9749d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161100 | ||||||
| chr7:117161113 | T | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0088 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.964-9749T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161113 | |||||||
| chr7:117161223 | A | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-9639A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161223 | |||||||
| chr7:117161269 | G | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-9593G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161269 | |||||||
| chr7:117161317 | G | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0061 others(17): Show |
20 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.964-9545G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161317 | |||||||
| chr7:117161506 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0115 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-9356G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161506 | |||||||
| chr7:117161591 | C | CT | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
113 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.964-9251dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161591 | ||||||
| chr7:117161591 | C | CTT | 13 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0063 others(10): Show |
13 | HG00323.hp1 HG00741.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-9252_964-9251d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161591 | ||||||
| chr7:117161591 | CT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0038 others(11): Show |
14 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.964-9251delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117161591 | ||||||
| chr7:117161596 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.964-9266T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161596 | |||||||
| chr7:117161600 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-9262T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161600 | |||||||
| chr7:117161703 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.964-9159G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161703 | |||||||
| chr7:117161739 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964-9123A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161739 | |||||||
| chr7:117161779 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.964-9083T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161779 | |||||||
| chr7:117161798 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(69): Show |
72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.964-9064T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161798 | |||||||
| chr7:117161955 | G | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.964-8907G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117161955 | |||||||
| chr7:117162037 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0035 others(2): Show |
5 | HG00408.hp1 HG02004.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-8825G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162037 | |||||||
| chr7:117162119 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0098 |
2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.964-8743T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162119 | |||||||
| chr7:117162218 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-8644T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162218 | |||||||
| chr7:117162254 | A | AT | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0148 |
3 | NA18960.hp2 NA18990.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.964-8607dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117162254 | ||||||
| chr7:117162258 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-8604G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162258 | |||||||
| chr7:117162336 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-8526G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162336 | |||||||
| chr7:117162728 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.964-8134A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162728 | |||||||
| chr7:117162744 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0042 |
3 | HG00408.hp1 HG02004.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.964-8118A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162744 | |||||||
| chr7:117162792 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964-8070A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117162792 | |||||||
| chr7:117163037 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-7825G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163037 | |||||||
| chr7:117163258 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.964-7604C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163258 | |||||||
| chr7:117163333 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(69): Show |
72 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.964-7529G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163333 | |||||||
| chr7:117163741 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-7121C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163741 | |||||||
| chr7:117163774 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.964-7088G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163774 | |||||||
| chr7:117163948 | A | G | 11 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0095 others(8): Show |
11 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.964-6914A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163948 | |||||||
| chr7:117163962 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0113 |
3 | HG04184.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.964-6900T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117163962 | |||||||
| chr7:117164269 | G | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0049 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.964-6593G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164269 | |||||||
| chr7:117164313 | A | AC | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(32): Show |
35 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-6542dupC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117164313 | ||||||
| chr7:117164551 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.964-6311A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164551 | |||||||
| chr7:117164627 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-6235C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164627 | |||||||
| chr7:117164876 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
77 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.964-5986A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164876 | |||||||
| chr7:117164880 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0113 |
3 | HG04184.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.964-5982G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164880 | |||||||
| chr7:117164983 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.964-5879G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117164983 | |||||||
| chr7:117165064 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.964-5798G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165064 | |||||||
| chr7:117165087 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG01192.hp2 HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.964-5775A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165087 | |||||||
| chr7:117165155 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.964-5707G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165155 | |||||||
| chr7:117165393 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964-5469G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165393 | |||||||
| chr7:117165437 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.964-5425G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165437 | |||||||
| chr7:117165454 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.964-5408G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165454 | |||||||
| chr7:117165458 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-5404C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165458 | |||||||
| chr7:117165814 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-5048G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165814 | |||||||
| chr7:117165868 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0128 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-4994G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117165868 | |||||||
| chr7:117166049 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.964-4813C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166049 | |||||||
| chr7:117166097 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.964-4765A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166097 | |||||||
| chr7:117166280 | T | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-4582T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166280 | |||||||
| chr7:117166450 | AT | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(68): Show |
71 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.964-4398delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117166450 | ||||||
| chr7:117166655 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.964-4207T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166655 | |||||||
| chr7:117166655 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.964-4207T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166655 | |||||||
| chr7:117166761 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0076 a0001c0001t0001g0116 |
3 | HG00280.hp1 HG01943.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.964-4101C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166761 | |||||||
| chr7:117166762 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0112 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-4100G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166762 | |||||||
| chr7:117166839 | A | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(18): Show |
21 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.964-4023A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166839 | |||||||
| chr7:117166890 | C | CA | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(38): Show |
41 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-3960dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117166890 | ||||||
| chr7:117166890 | C | CAA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0086 others(5): Show |
8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-3961_964-3960d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117166890 | ||||||
| chr7:117166908 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.964-3954T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117166908 | |||||||
| chr7:117167053 | C | CTT | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-3798_964-3797d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117167053 | ||||||
| chr7:117167070 | TG | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0159 |
2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.964-3791delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167070 | |||||||
| chr7:117167071 | G | GT | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-3783dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117167071 | ||||||
| chr7:117167103 | G | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0061 others(10): Show |
13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-3759G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167103 | |||||||
| chr7:117167173 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964-3689A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167173 | |||||||
| chr7:117167225 | C | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-3637C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167225 | |||||||
| chr7:117167319 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964-3543C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117167319 | |||||||
| chr7:117168024 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.964-2838T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168024 | |||||||
| chr7:117168272 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-2590G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168272 | |||||||
| chr7:117168436 | G | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(5): Show |
8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-2426G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168436 | |||||||
| chr7:117168613 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-2249C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168613 | |||||||
| chr7:117168719 | T | C | 20 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(17): Show |
20 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.964-2143T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168719 | |||||||
| chr7:117168966 | A | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0140 |
3 | HG02647.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.964-1896A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168966 | |||||||
| chr7:117168976 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-1886G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117168976 | |||||||
| chr7:117169104 | A | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-1758A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169104 | |||||||
| chr7:117169119 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(49): Show |
52 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.964-1743C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169119 | |||||||
| chr7:117169127 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1735A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169127 | |||||||
| chr7:117169128 | A | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1734A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169128 | |||||||
| chr7:117169135 | TC | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
48 | HG00408.hp2 HG00438.hp2 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.964-1725delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169135 | ||||||
| chr7:117169137 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.964-1725C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169137 | |||||||
| chr7:117169137 | CT | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(20): Show |
23 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.964-1709delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169137 | ||||||
| chr7:117169282 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0073 |
2 | HG01081.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.964-1580C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169282 | |||||||
| chr7:117169286 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1576T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169286 | |||||||
| chr7:117169456 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-1406A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169456 | |||||||
| chr7:117169568 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(5): Show |
8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-1294G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169568 | |||||||
| chr7:117169704 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.964-1158C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169704 | |||||||
| chr7:117169820 | TTTTG | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-1040_964-1037d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169820 | ||||||
| chr7:117169821 | TTTG | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0062 others(6): Show |
9 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-1039_964-1037d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117169821 | ||||||
| chr7:117169824 | G | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(23): Show |
26 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.964-1038G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169824 | |||||||
| chr7:117169921 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.964-941G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117169921 | |||||||
| chr7:117170079 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-783G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117170079 | |||||||
| chr7:117170680 | C | CAAAT | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.964-167_964-164dup others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117170680 | ||||||
| chr7:117170758 | TC | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-102delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr7 | 117170758 | ||||||
| chr7:117170764 | C | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.964-98C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117170764 | |||||||
| chr7:117170766 | G | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0170 a0001c0001t0001g0178 |
3 | HG01192.hp1 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.964-96G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 9/15 | chr7 | 117170766 | |||||||
| chr7:117170983 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
73 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1078+7T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117170983 | |||||||
| chr7:117171085 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+109T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171085 | |||||||
| chr7:117171255 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+279A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171255 | |||||||
| chr7:117171303 | T | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+327T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171303 | |||||||
| chr7:117171400 | A | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0112 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+424A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171400 | |||||||
| chr7:117171609 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+633C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117171609 | |||||||
| chr7:117171946 | C | CTTT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0054 others(21): Show |
24 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.1078+984_1078+986d others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117171946 | ||||||
| chr7:117171946 | C | CTTTT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(18): Show |
21 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.1078+983_1078+986d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117171946 | ||||||
| chr7:117171946 | CT | C | 7 | a0001c0001t0001g0068 a0001c0001t0001g0086 a0001c0001t0001g0089 others(4): Show |
7 | HG01256.hp2 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078+986delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117171946 | ||||||
| chr7:117172012 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0142 |
2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1078+1036A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172012 | |||||||
| chr7:117172037 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0106 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078+1061A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172037 | |||||||
| chr7:117172084 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+1108A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172084 | |||||||
| chr7:117172347 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1078+1371T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172347 | |||||||
| chr7:117172685 | C | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+1709C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172685 | |||||||
| chr7:117172730 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+1754A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172730 | |||||||
| chr7:117172761 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+1785G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172761 | |||||||
| chr7:117172786 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+1810A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172786 | |||||||
| chr7:117172920 | G | A | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(19): Show |
22 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1078+1944G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117172920 | |||||||
| chr7:117173186 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1078+2210A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117173186 | |||||||
| chr7:117173225 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1078+2249C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117173225 | |||||||
| chr7:117174041 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1078+3065C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174041 | |||||||
| chr7:117174180 | T | G | 21 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(18): Show |
21 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1078+3204T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174180 | |||||||
| chr7:117174273 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1078+3297G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174273 | |||||||
| chr7:117174511 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1078+3535C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174511 | |||||||
| chr7:117174721 | T | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+3745T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117174721 | |||||||
| chr7:117175017 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1078+4041G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175017 | |||||||
| chr7:117175101 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+4125T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175101 | |||||||
| chr7:117175103 | C | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4127C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175103 | |||||||
| chr7:117175205 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4229C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175205 | |||||||
| chr7:117175445 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4469C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175445 | |||||||
| chr7:117175457 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+4481A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175457 | |||||||
| chr7:117175543 | T | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(11): Show |
14 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078+4567T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175543 | |||||||
| chr7:117175934 | G | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(17): Show |
20 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1078+4958G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175934 | |||||||
| chr7:117175934 | GA | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0062 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1078+4959delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117175934 | |||||||
| chr7:117176230 | C | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+5254C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176230 | |||||||
| chr7:117176412 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+5436G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176412 | |||||||
| chr7:117176552 | T | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0184 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1078+5576T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176552 | |||||||
| chr7:117176883 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0159 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1078+5907T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117176883 | |||||||
| chr7:117177078 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+6102T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177078 | |||||||
| chr7:117177378 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0061 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1078+6402C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177378 | |||||||
| chr7:117177408 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078+6432T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177408 | |||||||
| chr7:117177584 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1078+6608G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177584 | |||||||
| chr7:117177738 | C | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1078+6762C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177738 | |||||||
| chr7:117177760 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0166 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1078+6784G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177760 | |||||||
| chr7:117177982 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1078+7006A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117177982 | |||||||
| chr7:117178239 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+7263T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178239 | |||||||
| chr7:117178275 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1078+7299A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178275 | |||||||
| chr7:117178327 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+7351A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178327 | |||||||
| chr7:117178464 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+7488T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178464 | |||||||
| chr7:117178534 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1078+7558G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178534 | |||||||
| chr7:117178774 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0115 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078+7798C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117178774 | |||||||
| chr7:117179081 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+8105C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179081 | |||||||
| chr7:117179098 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+8122C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179098 | |||||||
| chr7:117179456 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(52): Show |
55 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1078+8480T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179456 | |||||||
| chr7:117179621 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+8645T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179621 | |||||||
| chr7:117179854 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1078+8878A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179854 | |||||||
| chr7:117179876 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1078+8900G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117179876 | |||||||
| chr7:117180115 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1078+9139T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180115 | |||||||
| chr7:117180126 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1078+9150C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180126 | |||||||
| chr7:117180127 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+9151C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180127 | |||||||
| chr7:117180130 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+9154G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180130 | |||||||
| chr7:117180233 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-9088T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180233 | |||||||
| chr7:117180378 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-8943C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180378 | |||||||
| chr7:117180562 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1079-8759T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180562 | |||||||
| chr7:117180785 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-8536G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180785 | |||||||
| chr7:117180899 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079-8422G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117180899 | |||||||
| chr7:117181201 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1079-8120A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181201 | |||||||
| chr7:117181277 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0159 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1079-8044C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181277 | |||||||
| chr7:117181586 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1079-7735A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181586 | |||||||
| chr7:117181592 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1079-7729T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181592 | |||||||
| chr7:117181692 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(68): Show |
71 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1079-7629A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181692 | |||||||
| chr7:117181723 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1079-7598A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181723 | |||||||
| chr7:117181738 | C | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-7583C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117181738 | |||||||
| chr7:117182206 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-7115C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182206 | |||||||
| chr7:117182271 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-7050G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182271 | |||||||
| chr7:117182339 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1079-6982T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182339 | |||||||
| chr7:117182368 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1079-6953G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182368 | |||||||
| chr7:117182441 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0184 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1079-6880A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182441 | |||||||
| chr7:117182446 | G | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0115 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079-6875G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182446 | |||||||
| chr7:117182606 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1079-6715G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182606 | |||||||
| chr7:117182614 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1079-6707T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182614 | |||||||
| chr7:117182615 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1079-6706A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182615 | |||||||
| chr7:117182801 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1079-6520T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182801 | |||||||
| chr7:117182938 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1079-6383C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117182938 | |||||||
| chr7:117183100 | TTTTGTTT others(1): Show |
T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-6197_1079-619 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117183100 | ||||||
| chr7:117183100 | TTTTGTTT others(5): Show |
T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0104 |
2 | HG00280.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.1079-6201_1079-619 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117183100 | ||||||
| chr7:117183214 | A | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1079-6107A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183214 | |||||||
| chr7:117183280 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1079-6041T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183280 | |||||||
| chr7:117183287 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1079-6034G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183287 | |||||||
| chr7:117183350 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1079-5971C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183350 | |||||||
| chr7:117183755 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0112 others(4): Show |
7 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079-5566A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183755 | |||||||
| chr7:117183907 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1079-5414A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117183907 | |||||||
| chr7:117183992 | GACAAAAA others(5): Show |
G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0061 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-5316_1079-530 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117183992 | ||||||
| chr7:117184063 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0061 others(10): Show |
13 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1079-5258G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184063 | |||||||
| chr7:117184284 | TG | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(74): Show |
77 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1079-5036delG | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184284 | |||||||
| chr7:117184541 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079-4780G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184541 | |||||||
| chr7:117184582 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-4739G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184582 | |||||||
| chr7:117184660 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1079-4661A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184660 | |||||||
| chr7:117184704 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1079-4617G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184704 | |||||||
| chr7:117184868 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079-4453G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184868 | |||||||
| chr7:117184876 | A | G | 21 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0046 others(18): Show |
21 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1079-4445A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184876 | |||||||
| chr7:117184921 | T | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0125 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1079-4400T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184921 | |||||||
| chr7:117184924 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1079-4397T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184924 | |||||||
| chr7:117184943 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1079-4378C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184943 | |||||||
| chr7:117184969 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1079-4352T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117184969 | |||||||
| chr7:117185046 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1079-4275A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185046 | |||||||
| chr7:117185237 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1079-4084A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185237 | |||||||
| chr7:117185467 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079-3854C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185467 | |||||||
| chr7:117185571 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1079-3750C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185571 | |||||||
| chr7:117185596 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1079-3725A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185596 | |||||||
| chr7:117185647 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-3674C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185647 | |||||||
| chr7:117185794 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
74 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1079-3527A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117185794 | |||||||
| chr7:117186176 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1079-3145G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117186176 | |||||||
| chr7:117186435 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0061 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1079-2886C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117186435 | |||||||
| chr7:117186735 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1079-2586C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117186735 | |||||||
| chr7:117187088 | T | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-2233T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187088 | |||||||
| chr7:117187106 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-2215T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187106 | |||||||
| chr7:117187138 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1079-2183T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187138 | |||||||
| chr7:117187527 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-1794T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187527 | |||||||
| chr7:117187684 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1079-1637T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187684 | |||||||
| chr7:117187866 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1079-1455C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117187866 | |||||||
| chr7:117188007 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-1314G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117188007 | |||||||
| chr7:117188103 | A | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-1218A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117188103 | |||||||
| chr7:117188326 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0014 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1079-995G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117188326 | |||||||
| chr7:117188773 | T | TATATATA others(41): Show |
1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079-547_1079-546i others(50): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | ||||||
| chr7:117188773 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1079-547_1079-546i others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | ||||||
| chr7:117188773 | T | TATATATA others(15): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079-547_1079-546i others(24): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | ||||||
| chr7:117188773 | T | TATATATC others(3): Show |
38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079-547_1079-546i others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr7 | 117188773 | ||||||
| chr7:117189013 | G | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1079-308G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 10/15 | chr7 | 117189013 | |||||||
| chr7:117189409 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1151+16T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117189409 | |||||||
| chr7:117189569 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1151+176C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117189569 | |||||||
| chr7:117189685 | TA | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1151+294delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr7 | 117189685 | ||||||
| chr7:117190018 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1151+625G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190018 | |||||||
| chr7:117190049 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1151+656C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190049 | |||||||
| chr7:117190351 | C | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1152-483C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190351 | |||||||
| chr7:117190356 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1152-478G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190356 | |||||||
| chr7:117190423 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0142 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152-411C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190423 | |||||||
| chr7:117190680 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1152-154C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190680 | |||||||
| chr7:117190726 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1152-108A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 11/15 | chr7 | 117190726 | |||||||
| chr7:117191014 | G | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0086 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1254+78G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191014 | |||||||
| chr7:117191448 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1254+512G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191448 | |||||||
| chr7:117191449 | A | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+513A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191449 | |||||||
| chr7:117191887 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1254+951A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117191887 | |||||||
| chr7:117191961 | T | TATC | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
75 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1254+1027_1254+102 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117191961 | ||||||
| chr7:117192626 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0079 others(2): Show |
5 | HG01934.hp2 HG02071.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+1690C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192626 | |||||||
| chr7:117192866 | G | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0087 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1254+1930G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192866 | |||||||
| chr7:117192869 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1254+1933T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192869 | |||||||
| chr7:117192880 | G | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1254+1944G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192880 | |||||||
| chr7:117192905 | G | T | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1254+1969G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192905 | |||||||
| chr7:117192906 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1254+1970C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117192906 | |||||||
| chr7:117193124 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0180 |
2 | NA18981.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1254+2188T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193124 | |||||||
| chr7:117193150 | T | TAC | 6 | a0001c0001t0001g0057 a0001c0001t0001g0082 a0001c0001t0001g0108 others(3): Show |
6 | HG02965.hp2 HG03209.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254+2245_1254+224 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193150 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0113 |
2 | HG04184.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1254+2237_1254+224 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193150 | T | TACACACA others(5): Show |
11 | a0001c0001t0001g0023 a0001c0001t0001g0099 a0001c0001t0001g0125 others(8): Show |
11 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+2235_1254+224 others(16): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193150 | T | TACACACA others(7): Show |
16 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(13): Show |
16 | HG01192.hp2 HG01943.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1254+2233_1254+224 others(18): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193150 | T | TACACACA others(9): Show |
12 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0088 others(9): Show |
12 | HG00673.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1254+2231_1254+224 others(20): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193150 | T | TACACACA others(11): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0059 others(4): Show |
7 | HG02055.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+2229_1254+224 others(22): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193150 | TACAC | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0049 others(12): Show |
15 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1254+2243_1254+224 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193150 | TACACAC | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0115 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+2241_1254+224 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117193150 | ||||||
| chr7:117193230 | G | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG01496.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+2294G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193230 | |||||||
| chr7:117193401 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1254+2465T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193401 | |||||||
| chr7:117193430 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
76 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1254+2494A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193430 | |||||||
| chr7:117193484 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1254+2548C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193484 | |||||||
| chr7:117193614 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
38 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1254+2678C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193614 | |||||||
| chr7:117193881 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1254+2945G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117193881 | |||||||
| chr7:117194118 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0061 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1254+3182C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194118 | |||||||
| chr7:117194294 | A | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0085 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+3358A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194294 | |||||||
| chr7:117194537 | T | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0115 a0001c0001t0001g0142 others(1): Show |
4 | HG02451.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+3601T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194537 | |||||||
| chr7:117194719 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(15): Show |
18 | HG01496.hp2 HG02572.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1254+3783T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194719 | |||||||
| chr7:117194809 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1254+3873C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117194809 | |||||||
| chr7:117195074 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1254+4138G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195074 | |||||||
| chr7:117195086 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1254+4150A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195086 | |||||||
| chr7:117195154 | TA | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(45): Show |
48 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.1254+4227delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117195154 | ||||||
| chr7:117195169 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0062 others(8): Show |
11 | HG02572.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+4233A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195169 | |||||||
| chr7:117195170 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1254+4234T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195170 | |||||||
| chr7:117195349 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0069 others(1): Show |
4 | HG02280.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+4413T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195349 | |||||||
| chr7:117195680 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1254+4744C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195680 | |||||||
| chr7:117195817 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1254+4881C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195817 | |||||||
| chr7:117195838 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0052 others(6): Show |
9 | HG02280.hp1 HG02895.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+4902C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117195838 | |||||||
| chr7:117196386 | CCAACA | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1254+5451_1254+545 others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196386 | |||||||
| chr7:117196514 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0064 a0001c0001t0001g0184 |
3 | HG01496.hp2 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1254+5578G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196514 | |||||||
| chr7:117196619 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1254+5683T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196619 | |||||||
| chr7:117196624 | C | CT | 11 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(8): Show |
11 | HG01433.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1254+5715dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | ||||||
| chr7:117196624 | C | CTTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG02615.hp2 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+5713_1254+571 others(7): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | ||||||
| chr7:117196624 | CT | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0086 a0001c0001t0001g0089 others(4): Show |
7 | HG02451.hp2 HG02647.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+5715delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | ||||||
| chr7:117196624 | CTTTT | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0139 others(2): Show |
5 | HG03098.hp2 HG03492.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+5712_1254+571 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | ||||||
| chr7:117196624 | CTTTTT | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(93): Show |
96 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1254+5711_1254+571 others(9): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | ||||||
| chr7:117196624 | CTTTTTTT others(3): Show |
C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1254+5706_1254+571 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196624 | ||||||
| chr7:117196680 | G | GTTTTCAA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1254+5746_1254+575 others(11): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117196680 | ||||||
| chr7:117196852 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0126 |
3 | HG00741.hp2 HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1254+5916T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196852 | |||||||
| chr7:117196940 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0106 a0001c0001t0001g0122 |
3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1254+6004A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117196940 | |||||||
| chr7:117197556 | T | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1254+6620T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117197556 | |||||||
| chr7:117197738 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1254+6802A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117197738 | |||||||
| chr7:117198257 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1254+7321G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198257 | |||||||
| chr7:117198316 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1254+7380G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198316 | |||||||
| chr7:117198592 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1254+7656T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198592 | |||||||
| chr7:117198700 | CA | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1254+7765delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198700 | |||||||
| chr7:117198978 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1254+8042C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117198978 | |||||||
| chr7:117199184 | T | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1254+8248T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199184 | |||||||
| chr7:117199368 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1254+8432A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199368 | |||||||
| chr7:117199539 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1254+8603A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199539 | |||||||
| chr7:117199583 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1254+8647T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199583 | |||||||
| chr7:117199612 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0069 others(1): Show |
4 | HG02280.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+8676A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199612 | |||||||
| chr7:117199666 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1254+8730T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199666 | |||||||
| chr7:117199685 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1254+8749C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199685 | |||||||
| chr7:117199691 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1254+8755C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199691 | |||||||
| chr7:117199811 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1254+8875A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199811 | |||||||
| chr7:117199896 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1254+8960C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117199896 | |||||||
| chr7:117200026 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0142 |
2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+9090C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200026 | |||||||
| chr7:117200154 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1254+9218T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200154 | |||||||
| chr7:117200438 | C | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1255-9349C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200438 | |||||||
| chr7:117200742 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1255-9045C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200742 | |||||||
| chr7:117200779 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1255-9008A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200779 | |||||||
| chr7:117200818 | CT | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
111 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1255-8953delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200818 | ||||||
| chr7:117200818 | CTT | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0026 others(28): Show |
31 | HG00323.hp2 HG00408.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1255-8954_1255-895 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200818 | ||||||
| chr7:117200833 | T | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
53 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1255-8954T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200833 | |||||||
| chr7:117200834 | T | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1255-8953T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200834 | |||||||
| chr7:117200834 | TA | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0052 others(14): Show |
17 | HG02258.hp1 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1255-8943delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200834 | ||||||
| chr7:117200834 | TAA | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0088 others(1): Show |
4 | HG02976.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-8944_1255-894 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117200834 | ||||||
| chr7:117200836 | A | T | 8 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255-8951A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200836 | |||||||
| chr7:117200889 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1255-8898A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117200889 | |||||||
| chr7:117201060 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1255-8727A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201060 | |||||||
| chr7:117201112 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0086 a0001c0001t0001g0089 others(4): Show |
7 | HG02647.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1255-8675G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201112 | |||||||
| chr7:117201197 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1255-8590A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201197 | |||||||
| chr7:117201310 | C | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0043 others(33): Show |
36 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1255-8477C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201310 | |||||||
| chr7:117201445 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1255-8342C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201445 | |||||||
| chr7:117201560 | G | GT | 47 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0043 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG02027.hp2 others(44): Show |
intron_variant | MODIFIER | c.1255-8215dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117201560 | ||||||
| chr7:117201617 | G | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1255-8170G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201617 | |||||||
| chr7:117201644 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0154 |
3 | HG01934.hp1 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1255-8143G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201644 | |||||||
| chr7:117201820 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1255-7967C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201820 | |||||||
| chr7:117201894 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-7893G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201894 | |||||||
| chr7:117201900 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1255-7887A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201900 | |||||||
| chr7:117201949 | GCTCGAAG others(304): Show |
G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1255-7823_1255-751 others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117201949 | ||||||
| chr7:117201961 | C | CT | 30 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0043 others(27): Show |
30 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.1255-7809dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117201961 | ||||||
| chr7:117201963 | T | TG | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-7824_1255-782 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117201963 | |||||||
| chr7:117202587 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1255-7200C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202587 | |||||||
| chr7:117202734 | A | C | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-7053A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202734 | |||||||
| chr7:117202792 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1255-6995G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202792 | |||||||
| chr7:117202863 | GT | G | 13 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1255-6917delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117202863 | ||||||
| chr7:117202870 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1255-6917T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202870 | |||||||
| chr7:117202876 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1255-6911C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202876 | |||||||
| chr7:117202894 | A | T | 8 | a0001c0001t0001g0032 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG00408.hp2 HG00438.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1255-6893A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202894 | |||||||
| chr7:117202895 | T | G | 1 | a0001c0001t0001g0028 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1255-6892T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117202895 | |||||||
| chr7:117203002 | G | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1255-6785G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117203002 | |||||||
| chr7:117203030 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0142 |
2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1255-6757A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117203030 | |||||||
| chr7:117203046 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1255-6741G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117203046 | |||||||
| chr7:117204074 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1255-5713G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204074 | |||||||
| chr7:117204297 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1255-5490T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204297 | |||||||
| chr7:117204566 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1255-5221T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204566 | |||||||
| chr7:117204571 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1255-5216T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204571 | |||||||
| chr7:117204705 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-5082A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204705 | |||||||
| chr7:117204889 | G | T | 14 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1255-4898G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204889 | |||||||
| chr7:117204901 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1255-4886A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204901 | |||||||
| chr7:117204927 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1255-4860C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117204927 | |||||||
| chr7:117205197 | CTACCTA | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0098 a0001c0001t0001g0104 others(1): Show |
4 | HG00099.hp1 HG00280.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-4584_1255-457 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117205197 | ||||||
| chr7:117205203 | A | G | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-4584A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205203 | |||||||
| chr7:117205207 | C | CT | 21 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(18): Show |
21 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1255-4573dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117205207 | ||||||
| chr7:117205463 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1255-4324G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205463 | |||||||
| chr7:117205536 | T | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-4251T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205536 | |||||||
| chr7:117205657 | A | G | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-4130A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205657 | |||||||
| chr7:117205784 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1255-4003A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205784 | |||||||
| chr7:117205910 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1255-3877A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117205910 | |||||||
| chr7:117206185 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-3602G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206185 | |||||||
| chr7:117206225 | G | T | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-3562G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206225 | |||||||
| chr7:117206402 | A | G | 21 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(18): Show |
21 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1255-3385A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206402 | |||||||
| chr7:117206435 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1255-3352G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206435 | |||||||
| chr7:117206803 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1255-2984A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206803 | |||||||
| chr7:117206846 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1255-2941A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206846 | |||||||
| chr7:117206890 | T | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0166 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1255-2897T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117206890 | |||||||
| chr7:117207149 | A | AT | 12 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0086 others(9): Show |
12 | HG00438.hp2 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1255-2624dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117207149 | ||||||
| chr7:117207149 | AT | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
113 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1255-2624delT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117207149 | ||||||
| chr7:117207151 | T | TG | 13 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1255-2636_1255-263 others(5): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207151 | |||||||
| chr7:117207246 | A | G | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-2541A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207246 | |||||||
| chr7:117207431 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-2356C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207431 | |||||||
| chr7:117207497 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1255-2290C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207497 | |||||||
| chr7:117207503 | C | T | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-2284C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207503 | |||||||
| chr7:117207664 | T | TA | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-2122dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117207664 | ||||||
| chr7:117207701 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1255-2086T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117207701 | |||||||
| chr7:117208140 | T | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1255-1647T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208140 | |||||||
| chr7:117208262 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0097 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-1525A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208262 | |||||||
| chr7:117208366 | C | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1255-1421C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208366 | |||||||
| chr7:117208576 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1255-1211A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208576 | |||||||
| chr7:117208682 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1255-1105A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208682 | |||||||
| chr7:117208786 | G | A | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-1001G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208786 | |||||||
| chr7:117208902 | G | GGTGT | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG02109.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1255-846_1255-843d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | ||||||
| chr7:117208902 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1255-885G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208902 | |||||||
| chr7:117208902 | GGT | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0063 others(3): Show |
6 | HG01978.hp2 HG02257.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-844_1255-843d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | ||||||
| chr7:117208902 | GGTGT | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0045 others(12): Show |
15 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255-846_1255-843d others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | ||||||
| chr7:117208902 | GGTGTGT | G | 7 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0113 others(4): Show |
7 | HG00741.hp1 HG02040.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-848_1255-843d others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | ||||||
| chr7:117208902 | GGTGTGTG others(1): Show |
G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1255-850_1255-843d others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | ||||||
| chr7:117208902 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1255-852_1255-843d others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | ||||||
| chr7:117208902 | GGTGTGTG others(5): Show |
G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0153 a0001c0001t0001g0159 |
3 | NA18965.hp2 NA18971.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1255-854_1255-843d others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr7 | 117208902 | ||||||
| chr7:117208910 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-877T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117208910 | |||||||
| chr7:117209045 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1255-742G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209045 | |||||||
| chr7:117209056 | G | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0149 |
2 | NA18973.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1255-731G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209056 | |||||||
| chr7:117209273 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1255-514G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209273 | |||||||
| chr7:117209401 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0107 |
2 | HG00741.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1255-386A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209401 | |||||||
| chr7:117209519 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0159 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1255-268T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209519 | |||||||
| chr7:117209671 | G | C | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1255-116G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 12/15 | chr7 | 117209671 | |||||||
| chr7:117210306 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1405+369G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210306 | |||||||
| chr7:117210499 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0103 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1405+562A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210499 | |||||||
| chr7:117210528 | T | C | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+591T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210528 | |||||||
| chr7:117210716 | C | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1405+779C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210716 | |||||||
| chr7:117210776 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1405+839G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117210776 | |||||||
| chr7:117211043 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0112 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1405+1106T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211043 | |||||||
| chr7:117211103 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0052 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1405+1166G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211103 | |||||||
| chr7:117211299 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1405+1362C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211299 | |||||||
| chr7:117211427 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0164 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1405+1490A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211427 | |||||||
| chr7:117211438 | T | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0151 |
2 | HG02027.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1405+1501T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211438 | |||||||
| chr7:117211481 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1405+1544G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211481 | |||||||
| chr7:117211526 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0097 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+1589A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211526 | |||||||
| chr7:117211685 | G | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1405+1748G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211685 | |||||||
| chr7:117211921 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1405+1984G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117211921 | |||||||
| chr7:117212177 | G | A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
14 | HG00408.hp1 HG01934.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1405+2240G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212177 | |||||||
| chr7:117212347 | C | G | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+2410C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212347 | |||||||
| chr7:117212659 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1405+2722T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212659 | |||||||
| chr7:117212702 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1405+2765T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212702 | |||||||
| chr7:117212758 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0112 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1405+2821A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212758 | |||||||
| chr7:117212886 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1405+2949A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117212886 | |||||||
| chr7:117213079 | C | T | 4 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0097 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+3142C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213079 | |||||||
| chr7:117213226 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1405+3289G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213226 | |||||||
| chr7:117213306 | T | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1405+3369T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213306 | |||||||
| chr7:117213356 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1405+3419A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213356 | |||||||
| chr7:117213636 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1405+3699G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213636 | |||||||
| chr7:117213641 | TA | T | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+3715delA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117213641 | ||||||
| chr7:117213643 | A | T | 13 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1405+3706A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213643 | |||||||
| chr7:117213708 | T | G | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1405+3771T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213708 | |||||||
| chr7:117213741 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0014 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1405+3804A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213741 | |||||||
| chr7:117213876 | G | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1405+3939G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213876 | |||||||
| chr7:117213940 | C | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1405+4003C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213940 | |||||||
| chr7:117213969 | G | A | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+4032G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117213969 | |||||||
| chr7:117214151 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1405+4214C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214151 | |||||||
| chr7:117214208 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1405+4271A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214208 | |||||||
| chr7:117214273 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1405+4336A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214273 | |||||||
| chr7:117214291 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0187 |
2 | NA19000.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1405+4354C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214291 | |||||||
| chr7:117214375 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0112 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1405+4438G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214375 | |||||||
| chr7:117214725 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0016 others(2): Show |
5 | HG03492.hp2 HG04228.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406-4359C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214725 | |||||||
| chr7:117214749 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1406-4335C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214749 | |||||||
| chr7:117214795 | G | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-4289G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214795 | |||||||
| chr7:117214910 | T | TTG | 4 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0116 others(1): Show |
4 | HG00738.hp1 HG01943.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1406-4130_1406-412 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214910 | TTG | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(7): Show |
10 | HG01192.hp1 HG01358.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1406-4130_1406-412 others(6): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214910 | TTGTG | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0040 others(9): Show |
12 | HG01071.hp2 HG02040.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1406-4132_1406-412 others(8): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214910 | TTGTGTG | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(82): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1406-4134_1406-412 others(10): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214910 | TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0088 others(6): Show |
9 | HG00642.hp1 HG01081.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1406-4136_1406-412 others(12): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214910 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | HG00323.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406-4138_1406-412 others(14): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214910 | TTGTGTGT others(15): Show |
T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0052 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-4150_1406-412 others(26): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214910 | TTGTGTGT others(17): Show |
T | 23 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(20): Show |
23 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-4152_1406-412 others(28): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117214910 | ||||||
| chr7:117214958 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1406-4126A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214958 | |||||||
| chr7:117214977 | T | C | 27 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0052 others(24): Show |
27 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1406-4107T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117214977 | |||||||
| chr7:117215037 | G | A | 18 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(15): Show |
18 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1406-4047G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215037 | |||||||
| chr7:117215059 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1406-4025A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215059 | |||||||
| chr7:117215326 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0112 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1406-3758G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215326 | |||||||
| chr7:117215355 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0103 |
3 | HG01433.hp1 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1406-3729T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215355 | |||||||
| chr7:117215787 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1406-3297A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117215787 | |||||||
| chr7:117216082 | TC | T | 4 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0097 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-2996delC | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117216082 | ||||||
| chr7:117216129 | A | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1406-2955A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216129 | |||||||
| chr7:117216146 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1406-2938T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216146 | |||||||
| chr7:117216590 | G | C | 47 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0032 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(44): Show |
intron_variant | MODIFIER | c.1406-2494G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216590 | |||||||
| chr7:117216619 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1406-2465A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117216619 | |||||||
| chr7:117217178 | A | T | 1 | a0001c0001t0001g0172 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1406-1906A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217178 | |||||||
| chr7:117217288 | G | GA | 17 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0045 others(14): Show |
17 | HG00673.hp2 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1406-1785dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117217288 | ||||||
| chr7:117217296 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1406-1788A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217296 | |||||||
| chr7:117217300 | C | A | 23 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(20): Show |
23 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-1784C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217300 | |||||||
| chr7:117217304 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1406-1780A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217304 | |||||||
| chr7:117217319 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1406-1765C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217319 | |||||||
| chr7:117217493 | G | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0054 others(16): Show |
19 | HG00408.hp2 HG00438.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1406-1591G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217493 | |||||||
| chr7:117217622 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1406-1462C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217622 | |||||||
| chr7:117217686 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1406-1398A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117217686 | |||||||
| chr7:117218187 | A | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0142 |
2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1406-897A>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218187 | |||||||
| chr7:117218330 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1406-754A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218330 | |||||||
| chr7:117218344 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1406-740G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218344 | |||||||
| chr7:117218754 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0166 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1406-330A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218754 | |||||||
| chr7:117218886 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1406-198A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117218886 | |||||||
| chr7:117218900 | A | ATG | 3 | a0001c0001t0001g0052 a0001c0001t0001g0166 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1406-179_1406-178d others(4): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr7 | 117218900 | ||||||
| chr7:117219073 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1406-11C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 13/15 | chr7 | 117219073 | |||||||
| chr7:117219219 | A | T | 1 | a0001c0001t0001g0014 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498+43A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219219 | |||||||
| chr7:117219638 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(9): Show |
12 | HG01081.hp1 HG01192.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1498+462T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219638 | |||||||
| chr7:117219728 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1498+552C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219728 | |||||||
| chr7:117219801 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0151 |
2 | HG02027.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1498+625G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219801 | |||||||
| chr7:117219806 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1498+630C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219806 | |||||||
| chr7:117219861 | G | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1498+685G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219861 | |||||||
| chr7:117219948 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1498+772T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117219948 | |||||||
| chr7:117220075 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1498+899A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220075 | |||||||
| chr7:117220139 | G | C | 20 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(17): Show |
20 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1498+963G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220139 | |||||||
| chr7:117220227 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1498+1051A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220227 | |||||||
| chr7:117220247 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1498+1071G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220247 | |||||||
| chr7:117220271 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1498+1095C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220271 | |||||||
| chr7:117220306 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0166 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1498+1130G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220306 | |||||||
| chr7:117220771 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1499-1152C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117220771 | |||||||
| chr7:117221091 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
102 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1499-832C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221091 | |||||||
| chr7:117221199 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1499-724T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221199 | |||||||
| chr7:117221492 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0055 others(1): Show |
4 | HG02258.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-431A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221492 | |||||||
| chr7:117221615 | G | GA | 5 | a0001c0001t0001g0025 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG02071.hp2 HG02083.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-301dupA | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr7 | 117221615 | ||||||
| chr7:117221760 | G | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0142 a0001c0001t0001g0145 |
3 | HG02895.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1499-163G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 14/15 | chr7 | 117221760 | |||||||
| chr7:117222204 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1638+142T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222204 | |||||||
| chr7:117222206 | G | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1638+144G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222206 | |||||||
| chr7:117222475 | A | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
8 | HG00408.hp1 HG01934.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1638+413A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222475 | |||||||
| chr7:117222554 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638+492G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222554 | |||||||
| chr7:117222650 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0069 others(1): Show |
4 | HG02280.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1638+588G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222650 | |||||||
| chr7:117222862 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1638+800T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222862 | |||||||
| chr7:117222922 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1638+860G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222922 | |||||||
| chr7:117222950 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1638+888G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117222950 | |||||||
| chr7:117223041 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1638+979G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223041 | |||||||
| chr7:117223074 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1638+1012G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223074 | |||||||
| chr7:117223278 | C | T | 14 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1638+1216C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223278 | |||||||
| chr7:117223449 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638+1387G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223449 | |||||||
| chr7:117223608 | ACTGTCAC others(4): Show |
A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0142 a0001c0001t0001g0145 |
3 | HG02895.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1638+1550_1638+156 others(15): Show |
ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr7 | 117223608 | ||||||
| chr7:117223735 | G | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(25): Show |
28 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1638+1673G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117223735 | |||||||
| chr7:117224277 | C | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0020 others(38): Show |
41 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1638+2215C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224277 | |||||||
| chr7:117224466 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0180 |
2 | NA19004.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1638+2404C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224466 | |||||||
| chr7:117224836 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1638+2774C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224836 | |||||||
| chr7:117224995 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1638+2933G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117224995 | |||||||
| chr7:117225145 | G | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1638+3083G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225145 | |||||||
| chr7:117225145 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1638+3083G>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225145 | |||||||
| chr7:117225251 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1638+3189T>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225251 | |||||||
| chr7:117225355 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1638+3293C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225355 | |||||||
| chr7:117225681 | A | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0064 a0001c0001t0001g0184 |
3 | HG01496.hp2 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1638+3619A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225681 | |||||||
| chr7:117225831 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1638+3769C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117225831 | |||||||
| chr7:117226143 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1639-3619A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226143 | |||||||
| chr7:117226262 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1639-3500A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226262 | |||||||
| chr7:117226719 | C | G | 14 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1639-3043C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226719 | |||||||
| chr7:117226757 | C | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(80): Show |
83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639-3005C>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226757 | |||||||
| chr7:117226822 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1639-2940T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117226822 | |||||||
| chr7:117227030 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(80): Show |
83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639-2732C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227030 | |||||||
| chr7:117227212 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1639-2550G>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227212 | |||||||
| chr7:117227241 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(32): Show |
35 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1639-2521C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227241 | |||||||
| chr7:117227242 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0167 |
2 | HG03139.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1639-2520G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227242 | |||||||
| chr7:117227600 | G | GT | 3 | a0001c0001t0001g0052 a0001c0001t0001g0166 a0001c0002t0001g0044 |
3 | HG02970.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1639-2161dupT | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr7 | 117227600 | ||||||
| chr7:117227743 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0129 a0001c0001t0001g0147 others(2): Show |
5 | HG01255.hp1 HG01256.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1639-2019A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227743 | |||||||
| chr7:117227802 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0112 |
3 | HG02630.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1639-1960C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227802 | |||||||
| chr7:117227876 | G | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0047 others(10): Show |
13 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1639-1886G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117227876 | |||||||
| chr7:117228095 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0112 |
3 | HG02630.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1639-1667G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228095 | |||||||
| chr7:117228133 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0142 a0001c0001t0001g0145 |
3 | HG02895.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1639-1629C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228133 | |||||||
| chr7:117228357 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1639-1405T>C | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228357 | |||||||
| chr7:117228518 | T | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(32): Show |
35 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1639-1244T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228518 | |||||||
| chr7:117228525 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1639-1237G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228525 | |||||||
| chr7:117228531 | T | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(80): Show |
83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639-1231T>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228531 | |||||||
| chr7:117228642 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(32): Show |
35 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1639-1120C>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228642 | |||||||
| chr7:117228763 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1639-999G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228763 | |||||||
| chr7:117228766 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1639-996C>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228766 | |||||||
| chr7:117228779 | A | G | 1 | a0001c0001t0001g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1639-983A>G | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117228779 | |||||||
| chr7:117229183 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1639-579G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117229183 | |||||||
| chr7:117229425 | A | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0126 |
3 | HG00741.hp2 HG01256.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1639-337A>T | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117229425 | |||||||
| chr7:117229687 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1639-75G>A | ST7 | ENSG00000004866.22 | transcript | ENST00000323984.8 | protein_coding | 15/15 | chr7 | 117229687 |