Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5191 |
| ensemblid | ENSG00000112357.14 |
| hgncid | 8860 |
| symbol | PEX7 |
| name | peroxisomal biogenesis factor 7 |
| refseq_nuc | NM_000288.4 |
| refseq_prot | NP_000279.1 |
| ensembl_nuc | ENST00000318471.5 |
| ensembl_prot | ENSP00000315680.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 136822592 |
| end | 136913934 |
| strand | + |
| ver | v1.2 |
| region | chr6:136822592-136913934 |
| region5000 | chr6:136817592-136918934 |
| regionname0 | PEX7_chr6_136822592_136913934 |
| regionname5000 | PEX7_chr6_136817592_136918934 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 323 | 329 | 92 | 61 | 132 | 12 | 30 | 98 | PEX7_chr6_136817592_136918934 | PEX7 | MSAVC others(318): Show |
chr6 | 136817592 | 136918934 |
| a0002 | 0/0 | 323 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | MSAVC others(318): Show |
chr6 | 136817592 | 136918934 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 969 | 329 | 92 | 61 | 132 | 12 | 30 | PEX7_chr6_136817592_136918934 | PEX7 | ATGAG others(964): Show |
chr6 | 136817592 | 136918934 | ||
| a0002c0002 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | ATGAG others(964): Show |
chr6 | 136817592 | 136918934 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1454 | 144 | 22 | 36 | 62 | 8 | 14 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1449): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0002 | 0/0 | 1457 | 142 | 31 | 23 | 69 | 4 | 15 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0003 | 0/0 | 1453 | 14 | 14 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1448): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0004 | 0/0 | 1457 | 11 | 9 | 1 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0005 | 0/0 | 1454 | 6 | 5 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1449): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0006 | 0/0 | 1457 | 4 | 4 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0007 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1449): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0008 | 0/0 | 1457 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0009 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0010 | 0/0 | 1457 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| a0001c0001t0011 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| a0002c0002t0004 | 0/0 | 1457 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | AACCG others(1452): Show |
chr6 | 136817592 | 136918934 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0010 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0002 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| a0002c0002t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | FIN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01255 | hp2 | a0002 | c0002 | t0004 | g0147 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0282 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0278 | EUR | IBS | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0148 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CDX | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0151 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0289 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0123 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0291 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ESN | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | GWD | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0146 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | STU | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0290 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18947 | hp1 | a0001 | c0001 | t0010 | g0262 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | LWK | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | LWK | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | YRI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | TSI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | GIH | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0032 | REF | REF | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | PEX7_chr6_136817592_136918934 | PEX7 | chr6 | 136817592 | 136918934 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:136822793 | C | T | 1 | a0002 | 1 | HG01255.hp2 | missense_variant&splice_region_variant | MODERATE | c.128C>T | p.Ala43Val | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | 202/1454 | 128/972 | 43/323 | chr6 | 136822793 | |||
| chr6:136913929 | AT | A | 1 | a0001 | 14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
splice_region_variant | LOW | c.*407delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 136913929 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:136822601 | A | T | 1 | a0001c0001t0006 | 4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-65A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | chr6 | 136822601 | |||||||
| chr6:136822610 | C | T | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(4): Show |
38 | HG00639.hp2 HG01255.hp2 HG01884.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-56C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | 56 | chr6 | 136822610 | ||||||
| chr6:136822635 | G | A | 2 | a0001c0001t0007 a0001c0001t0008 |
5 | HG02622.hp1 HG02970.hp1 HG03139.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-31G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/10 | 31 | chr6 | 136822635 | ||||||
| chr6:136913613 | A | G | 1 | a0001c0001t0010 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | 87 | chr6 | 136913613 | ||||||
| chr6:136913781 | T | TGTA | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(5): Show |
163 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*257_*258insAGT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | 258 | INFO_REALIGN_3_PRIME | chr6 | 136913781 | |||||
| chr6:136913832 | T | G | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(3): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*306T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 10/10 | 306 | chr6 | 136913832 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:136822842 | G | GGGGGCC | 154 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(151): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.130+48_130+53dupGG others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 136822842 | ||||||
| chr6:136822888 | C | T | 1 | a0001c0001t0002g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.130+93C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136822888 | |||||||
| chr6:136822889 | T | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+94T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136822889 | |||||||
| chr6:136822946 | C | T | 1 | a0001c0001t0006g0295 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130+151C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136822946 | |||||||
| chr6:136823011 | C | A | 1 | a0001c0001t0002g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.130+216C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823011 | |||||||
| chr6:136823080 | G | C | 4 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+285G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823080 | |||||||
| chr6:136823105 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0177 others(1): Show |
5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+310G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823105 | |||||||
| chr6:136823152 | C | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.130+357C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823152 | |||||||
| chr6:136823166 | G | T | 1 | a0001c0001t0009g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+371G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823166 | |||||||
| chr6:136823217 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.130+422A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823217 | |||||||
| chr6:136823306 | C | T | 1 | a0001c0001t0009g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+511C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823306 | |||||||
| chr6:136823500 | A | G | 159 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(156): Show |
171 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.130+705A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823500 | |||||||
| chr6:136823614 | C | G | 212 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(209): Show |
230 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.130+819C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823614 | |||||||
| chr6:136823688 | C | A | 1 | a0001c0001t0002g0179 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130+893C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823688 | |||||||
| chr6:136823729 | G | C | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.130+934G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823729 | |||||||
| chr6:136823745 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.130+950C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823745 | |||||||
| chr6:136823782 | C | T | 148 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(145): Show |
160 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.130+987C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823782 | |||||||
| chr6:136823847 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.130+1052G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136823847 | |||||||
| chr6:136824112 | C | A | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.131-1102C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824112 | |||||||
| chr6:136824112 | C | G | 1 | a0001c0001t0002g0293 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.131-1102C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824112 | |||||||
| chr6:136824538 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.131-676T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824538 | |||||||
| chr6:136824589 | A | G | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-625A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824589 | |||||||
| chr6:136824623 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.131-591A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824623 | |||||||
| chr6:136824675 | A | G | 4 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-539A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824675 | |||||||
| chr6:136824939 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.131-275A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136824939 | |||||||
| chr6:136825045 | A | G | 1 | a0001c0001t0009g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-169A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 1/9 | chr6 | 136825045 | |||||||
| chr6:136825504 | T | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.188+233T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825504 | |||||||
| chr6:136825524 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188+253C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825524 | |||||||
| chr6:136825673 | A | G | 1 | a0001c0001t0002g0292 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.188+402A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825673 | |||||||
| chr6:136825806 | T | G | 1 | a0001c0001t0002g0293 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.189-513T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825806 | |||||||
| chr6:136825813 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189-506G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136825813 | |||||||
| chr6:136826244 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.189-75A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136826244 | |||||||
| chr6:136826292 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189-27T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 2/9 | chr6 | 136826292 | |||||||
| chr6:136826553 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.339+84A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826553 | |||||||
| chr6:136826577 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01496.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.339+108C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826577 | |||||||
| chr6:136826635 | G | A | 23 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(20): Show |
27 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.339+166G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826635 | |||||||
| chr6:136826892 | A | G | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+423A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826892 | |||||||
| chr6:136826922 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.339+453T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136826922 | |||||||
| chr6:136827144 | T | A | 1 | a0001c0001t0002g0139 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.339+675T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827144 | |||||||
| chr6:136827182 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.339+713A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827182 | |||||||
| chr6:136827238 | G | T | 4 | a0001c0001t0006g0289 a0001c0001t0006g0290 a0001c0001t0006g0291 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+769G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827238 | |||||||
| chr6:136827370 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.339+901A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827370 | |||||||
| chr6:136827388 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.339+919T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827388 | |||||||
| chr6:136827392 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.339+923T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827392 | |||||||
| chr6:136827504 | T | TTG | 23 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(20): Show |
25 | HG00323.hp1 HG00597.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.339+1079_339+1080d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | T | TTGTG | 32 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(29): Show |
36 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.339+1077_339+1080d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | T | TTGTGTG | 17 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
18 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.339+1075_339+1080d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(6): Show |
10 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.339+1073_339+1080d others(10): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | TTG | T | 30 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0069 others(27): Show |
34 | HG00639.hp2 HG01169.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.339+1079_339+1080d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | TTGTG | T | 14 | a0001c0001t0001g0130 a0001c0001t0001g0157 a0001c0001t0001g0158 others(11): Show |
14 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.339+1077_339+1080d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | TTGTGTG | T | 10 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(7): Show |
10 | HG02027.hp1 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+1075_339+1080d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | TTGTGTGT others(1): Show |
T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0164 others(13): Show |
16 | HG01106.hp2 HG01433.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.339+1073_339+1080d others(10): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | TTGTGTGT others(3): Show |
T | 118 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0155 others(115): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.339+1071_339+1080d others(12): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | TTGTGTGT others(5): Show |
T | 11 | a0001c0001t0002g0021 a0001c0001t0002g0179 a0001c0001t0002g0186 others(8): Show |
12 | HG01106.hp1 HG01192.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.339+1069_339+1080d others(14): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827504 | TTGTGTGT others(7): Show |
T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.339+1067_339+1080d others(16): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136827504 | ||||||
| chr6:136827657 | C | T | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+1188C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827657 | |||||||
| chr6:136827687 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.339+1218C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827687 | |||||||
| chr6:136827766 | A | G | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+1297A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827766 | |||||||
| chr6:136827776 | C | G | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.339+1307C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827776 | |||||||
| chr6:136827951 | T | G | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.339+1482T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136827951 | |||||||
| chr6:136828073 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.339+1604A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828073 | |||||||
| chr6:136828093 | G | T | 181 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(178): Show |
198 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.339+1624G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828093 | |||||||
| chr6:136828139 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.339+1670A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828139 | |||||||
| chr6:136828304 | A | G | 23 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(20): Show |
27 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.339+1835A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828304 | |||||||
| chr6:136828399 | T | C | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+1930T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828399 | |||||||
| chr6:136828435 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.339+1966G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828435 | |||||||
| chr6:136828457 | A | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0288 |
3 | HG02056.hp2 NA18612.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.339+1988A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828457 | |||||||
| chr6:136828534 | G | T | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.339+2065G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828534 | |||||||
| chr6:136828627 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.339+2158C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828627 | |||||||
| chr6:136828628 | G | C | 4 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0177 others(1): Show |
5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+2159G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828628 | |||||||
| chr6:136828765 | C | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0177 others(1): Show |
5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+2296C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828765 | |||||||
| chr6:136828892 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.339+2423A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828892 | |||||||
| chr6:136828949 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.339+2480A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136828949 | |||||||
| chr6:136829024 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.339+2555A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829024 | |||||||
| chr6:136829026 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.339+2557C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829026 | |||||||
| chr6:136829273 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.339+2804T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829273 | |||||||
| chr6:136829305 | GC | G | 4 | a0001c0001t0001g0284 a0001c0001t0002g0023 a0001c0001t0002g0282 others(1): Show |
5 | HG01243.hp1 HG01433.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2839delC | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136829305 | ||||||
| chr6:136829309 | A | T | 4 | a0001c0001t0001g0284 a0001c0001t0002g0023 a0001c0001t0002g0282 others(1): Show |
5 | HG01243.hp1 HG01433.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2840A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829309 | |||||||
| chr6:136829356 | G | A | 214 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(211): Show |
232 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.339+2887G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829356 | |||||||
| chr6:136829405 | T | C | 196 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(193): Show |
213 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.339+2936T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829405 | |||||||
| chr6:136829566 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.339+3097C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829566 | |||||||
| chr6:136829597 | A | G | 4 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0177 others(1): Show |
5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+3128A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829597 | |||||||
| chr6:136829757 | C | T | 1 | a0001c0001t0008g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.339+3288C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829757 | |||||||
| chr6:136829758 | G | A | 22 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(19): Show |
26 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+3289G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829758 | |||||||
| chr6:136829987 | G | GT | 6 | a0001c0001t0001g0178 a0001c0001t0001g0279 a0001c0001t0001g0280 others(3): Show |
6 | HG01256.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+3530dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136829987 | ||||||
| chr6:136829987 | GT | G | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+3530delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136829987 | ||||||
| chr6:136829988 | T | G | 1 | a0001c0001t0008g0123 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.339+3519T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136829988 | |||||||
| chr6:136830041 | G | T | 6 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(3): Show |
6 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+3572G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830041 | |||||||
| chr6:136830123 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.339+3654A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830123 | |||||||
| chr6:136830160 | G | A | 9 | a0001c0001t0001g0124 a0001c0001t0004g0142 a0001c0001t0004g0143 others(6): Show |
9 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.339+3691G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830160 | |||||||
| chr6:136830630 | A | G | 4 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+4161A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830630 | |||||||
| chr6:136830693 | T | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.339+4224T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830693 | |||||||
| chr6:136830878 | CAT | C | 4 | a0001c0001t0006g0289 a0001c0001t0006g0290 a0001c0001t0006g0291 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+4412_339+4413d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136830878 | ||||||
| chr6:136830970 | T | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.339+4501T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136830970 | |||||||
| chr6:136831076 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.339+4607G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831076 | |||||||
| chr6:136831369 | C | T | 188 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(185): Show |
205 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.339+4900C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831369 | |||||||
| chr6:136831483 | T | C | 201 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(198): Show |
218 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.339+5014T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831483 | |||||||
| chr6:136831531 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.339+5062C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831531 | |||||||
| chr6:136831565 | A | G | 2 | a0001c0001t0004g0121 a0001c0001t0004g0122 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.339+5096A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831565 | |||||||
| chr6:136831646 | A | G | 4 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0177 others(1): Show |
5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+5177A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831646 | |||||||
| chr6:136831719 | G | A | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0144 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+5250G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831719 | |||||||
| chr6:136831796 | T | A | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.339+5327T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831796 | |||||||
| chr6:136831798 | C | G | 1 | a0001c0001t0002g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339+5329C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831798 | |||||||
| chr6:136831908 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.339+5439G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831908 | |||||||
| chr6:136831934 | G | A | 2 | a0001c0001t0005g0104 a0001c0001t0005g0105 |
2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.339+5465G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136831934 | |||||||
| chr6:136832048 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.339+5579T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832048 | |||||||
| chr6:136832192 | T | C | 196 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(193): Show |
213 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.339+5723T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832192 | |||||||
| chr6:136832221 | T | C | 2 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
2 | HG00741.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.339+5752T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832221 | |||||||
| chr6:136832449 | T | C | 6 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+5980T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832449 | |||||||
| chr6:136832517 | T | G | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(147): Show |
162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.339+6048T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832517 | |||||||
| chr6:136832560 | G | C | 1 | a0001c0001t0001g0033 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.339+6091G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832560 | |||||||
| chr6:136832667 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.339+6198C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832667 | |||||||
| chr6:136832668 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.339+6199G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832668 | |||||||
| chr6:136832723 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.339+6254A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832723 | |||||||
| chr6:136832836 | C | T | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(147): Show |
162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.339+6367C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832836 | |||||||
| chr6:136832912 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0035 others(2): Show |
9 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.339+6443T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136832912 | |||||||
| chr6:136833231 | G | C | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG02074.hp1 NA18944.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.339+6762G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833231 | |||||||
| chr6:136833268 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.339+6799C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833268 | |||||||
| chr6:136833388 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.339+6919G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833388 | |||||||
| chr6:136833460 | T | G | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.339+6991T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833460 | |||||||
| chr6:136833482 | G | A | 215 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(212): Show |
233 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.339+7013G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833482 | |||||||
| chr6:136833804 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339+7335A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833804 | |||||||
| chr6:136833889 | T | C | 22 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(19): Show |
26 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+7420T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136833889 | |||||||
| chr6:136834023 | A | C | 1 | a0001c0001t0002g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339+7554A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834023 | |||||||
| chr6:136834028 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.339+7559A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834028 | |||||||
| chr6:136834045 | C | T | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+7576C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834045 | |||||||
| chr6:136834094 | C | A | 1 | a0001c0001t0001g0015 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.339+7625C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834094 | |||||||
| chr6:136834108 | A | C | 4 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0177 others(1): Show |
5 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+7639A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834108 | |||||||
| chr6:136834215 | TG | T | 7 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0135 others(4): Show |
7 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+7748delG | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136834215 | ||||||
| chr6:136834361 | C | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(180): Show |
199 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.339+7892C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834361 | |||||||
| chr6:136834419 | G | C | 22 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(19): Show |
26 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+7950G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834419 | |||||||
| chr6:136834548 | T | A | 29 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0007 others(26): Show |
33 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.339+8079T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834548 | |||||||
| chr6:136834586 | A | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0144 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.339+8117A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834586 | |||||||
| chr6:136834625 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.339+8156T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834625 | |||||||
| chr6:136834672 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.339+8203C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834672 | |||||||
| chr6:136834704 | T | C | 14 | a0001c0001t0002g0017 a0001c0001t0002g0140 a0001c0001t0002g0141 others(11): Show |
15 | HG01255.hp2 HG01981.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.339+8235T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834704 | |||||||
| chr6:136834788 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG00642.hp2 HG01081.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+8319C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136834788 | |||||||
| chr6:136835004 | A | G | 1 | a0001c0001t0002g0276 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.339+8535A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835004 | |||||||
| chr6:136835020 | A | G | 1 | a0001c0001t0006g0291 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+8551A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835020 | |||||||
| chr6:136835125 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.339+8656G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835125 | |||||||
| chr6:136835285 | T | A | 2 | a0001c0001t0003g0110 a0001c0001t0003g0111 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.339+8816T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835285 | |||||||
| chr6:136835382 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.339+8913G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835382 | |||||||
| chr6:136835549 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.339+9080A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835549 | |||||||
| chr6:136835559 | T | A | 4 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+9090T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835559 | |||||||
| chr6:136835788 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0002g0275 a0001c0001t0008g0123 |
3 | HG01256.hp2 HG01358.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.339+9319A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835788 | |||||||
| chr6:136835875 | A | C | 4 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 others(1): Show |
4 | HG02622.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+9406A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136835875 | |||||||
| chr6:136836052 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.340-9563T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836052 | |||||||
| chr6:136836142 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.340-9473T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836142 | |||||||
| chr6:136836233 | AAG | A | 186 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(183): Show |
202 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.340-9377_340-9376d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136836233 | ||||||
| chr6:136836297 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.340-9318A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836297 | |||||||
| chr6:136836446 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.340-9169C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836446 | |||||||
| chr6:136836483 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.340-9132C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836483 | |||||||
| chr6:136836621 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.340-8994T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836621 | |||||||
| chr6:136836724 | G | A | 25 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0007 others(22): Show |
29 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.340-8891G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836724 | |||||||
| chr6:136836869 | C | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.340-8746C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836869 | |||||||
| chr6:136836900 | T | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0094 |
3 | HG01358.hp1 HG01981.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.340-8715T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136836900 | |||||||
| chr6:136837009 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.340-8606C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837009 | |||||||
| chr6:136837112 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0296 |
4 | HG02630.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-8503G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837112 | |||||||
| chr6:136837279 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0008g0028 |
3 | HG02622.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.340-8336G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837279 | |||||||
| chr6:136837317 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0002g0175 a0001c0001t0007g0025 others(3): Show |
6 | HG02622.hp1 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-8298G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837317 | |||||||
| chr6:136837341 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.340-8274G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837341 | |||||||
| chr6:136837361 | C | CA | 13 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0050 others(10): Show |
14 | HG02155.hp2 NA18612.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.340-8240dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAA | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-8243_340-8240d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAA | 20 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(17): Show |
24 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.340-8245_340-8240d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0125 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.340-8249_340-8240d others(12): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.340-8250_340-8240d others(13): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(3): Show |
6 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-8251_340-8240d others(14): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0008g0123 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.340-8252_340-8240d others(15): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0171 a0001c0001t0001g0284 a0001c0001t0002g0140 others(5): Show |
8 | HG01257.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-8253_340-8240d others(16): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(8): Show |
114 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0130 others(111): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.340-8240_340-8239i others(17): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(9): Show |
29 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0156 others(26): Show |
29 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.340-8240_340-8239i others(18): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837361 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.340-8240_340-8239i others(19): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837361 | ||||||
| chr6:136837391 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.340-8224A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837391 | |||||||
| chr6:136837506 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0002g0126 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.340-8109T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837506 | |||||||
| chr6:136837530 | T | C | 24 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(21): Show |
26 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.340-8085T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837530 | |||||||
| chr6:136837626 | G | C | 189 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(186): Show |
205 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.340-7989G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837626 | |||||||
| chr6:136837695 | A | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0169 others(1): Show |
4 | HG00423.hp2 HG00597.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-7920A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837695 | |||||||
| chr6:136837738 | C | T | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-7877C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837738 | |||||||
| chr6:136837812 | C | CCA | 21 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0059 others(18): Show |
21 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.340-7771_340-7770d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | ||||||
| chr6:136837812 | C | CCACA | 36 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0089 others(33): Show |
40 | HG00639.hp2 HG01081.hp2 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.340-7773_340-7770d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | ||||||
| chr6:136837812 | CCA | C | 68 | a0001c0001t0001g0016 a0001c0001t0001g0102 a0001c0001t0001g0154 others(65): Show |
74 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.340-7771_340-7770d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | ||||||
| chr6:136837812 | CCACACA | C | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-7775_340-7770d others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136837812 | ||||||
| chr6:136837813 | C | T | 21 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0023 others(18): Show |
23 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.340-7802C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837813 | |||||||
| chr6:136837815 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.340-7800C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837815 | |||||||
| chr6:136837869 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.340-7746G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136837869 | |||||||
| chr6:136838222 | A | G | 12 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-7393A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838222 | |||||||
| chr6:136838498 | C | A | 3 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0004g0144 |
3 | HG02559.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.340-7117C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838498 | |||||||
| chr6:136838543 | C | A | 3 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0134 |
3 | HG04204.hp1 NA18942.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.340-7072C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838543 | |||||||
| chr6:136838964 | A | G | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.340-6651A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136838964 | |||||||
| chr6:136839060 | G | T | 2 | a0001c0001t0004g0108 a0001c0001t0004g0109 |
2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.340-6555G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839060 | |||||||
| chr6:136839061 | G | T | 2 | a0001c0001t0004g0108 a0001c0001t0004g0109 |
2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.340-6554G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839061 | |||||||
| chr6:136839244 | T | A | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.340-6371T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839244 | |||||||
| chr6:136839273 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.340-6342C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839273 | |||||||
| chr6:136839364 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.340-6251G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839364 | |||||||
| chr6:136839368 | A | G | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-6247A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839368 | |||||||
| chr6:136839414 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.340-6201G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839414 | |||||||
| chr6:136839639 | T | A | 1 | a0001c0001t0002g0192 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.340-5976T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839639 | |||||||
| chr6:136839677 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-5938G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839677 | |||||||
| chr6:136839712 | A | G | 12 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-5903A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839712 | |||||||
| chr6:136839837 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.340-5778A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839837 | |||||||
| chr6:136839845 | A | G | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.340-5770A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136839845 | |||||||
| chr6:136840214 | A | C | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-5401A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840214 | |||||||
| chr6:136840368 | T | C | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.340-5247T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840368 | |||||||
| chr6:136840409 | G | A | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-5206G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840409 | |||||||
| chr6:136840455 | A | T | 1 | a0001c0001t0002g0285 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.340-5160A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840455 | |||||||
| chr6:136840508 | T | TGTA | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.340-5106_340-5105i others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136840508 | ||||||
| chr6:136840533 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.340-5082C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136840533 | |||||||
| chr6:136841084 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.340-4531C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841084 | |||||||
| chr6:136841159 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0094 |
3 | HG01358.hp1 HG01981.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.340-4456G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841159 | |||||||
| chr6:136841161 | G | C | 115 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(112): Show |
125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.340-4454G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841161 | |||||||
| chr6:136841390 | A | C | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-4225A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841390 | |||||||
| chr6:136841394 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0086 a0001c0001t0001g0174 |
4 | HG00639.hp1 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-4221C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841394 | |||||||
| chr6:136841413 | A | G | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(16): Show |
23 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.340-4202A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841413 | |||||||
| chr6:136841535 | T | C | 1 | a0001c0001t0002g0293 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.340-4080T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841535 | |||||||
| chr6:136841620 | C | G | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.340-3995C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841620 | |||||||
| chr6:136841774 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.340-3841G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841774 | |||||||
| chr6:136841824 | G | A | 204 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(201): Show |
221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.340-3791G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841824 | |||||||
| chr6:136841849 | G | A | 15 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0106 others(12): Show |
15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340-3766G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841849 | |||||||
| chr6:136841876 | G | A | 203 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(200): Show |
220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.340-3739G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841876 | |||||||
| chr6:136841904 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.340-3711A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841904 | |||||||
| chr6:136841907 | A | T | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-3708A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136841907 | |||||||
| chr6:136842002 | C | CT | 20 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(17): Show |
20 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.340-3599dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136842002 | ||||||
| chr6:136842275 | G | C | 1 | a0001c0001t0003g0012 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.340-3340G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842275 | |||||||
| chr6:136842285 | A | G | 201 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(198): Show |
218 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.340-3330A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842285 | |||||||
| chr6:136842308 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-3307A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842308 | |||||||
| chr6:136842466 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.340-3149T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842466 | |||||||
| chr6:136842481 | C | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-3134C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842481 | |||||||
| chr6:136842586 | A | AT | 2 | a0001c0001t0002g0023 a0001c0001t0002g0283 |
3 | HG01243.hp1 HG01433.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.340-3026dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136842586 | ||||||
| chr6:136842761 | G | C | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-2854G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136842761 | |||||||
| chr6:136843021 | G | A | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-2594G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843021 | |||||||
| chr6:136843275 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.340-2340A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843275 | |||||||
| chr6:136843444 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.340-2171G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843444 | |||||||
| chr6:136843458 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.340-2157G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843458 | |||||||
| chr6:136843484 | G | T | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.340-2131G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843484 | |||||||
| chr6:136843660 | T | C | 156 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(153): Show |
169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.340-1955T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843660 | |||||||
| chr6:136843699 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.340-1916C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843699 | |||||||
| chr6:136843861 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.340-1754G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843861 | |||||||
| chr6:136843914 | C | T | 7 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0134 others(4): Show |
7 | HG02027.hp1 HG04204.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1701C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843914 | |||||||
| chr6:136843994 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG00544.hp2 HG00558.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-1621A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136843994 | |||||||
| chr6:136844092 | C | T | 12 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-1523C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844092 | |||||||
| chr6:136844111 | A | T | 203 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(200): Show |
220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.340-1504A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844111 | |||||||
| chr6:136844135 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0002g0260 |
2 | NA18960.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.340-1480C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844135 | |||||||
| chr6:136844349 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.340-1266C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844349 | |||||||
| chr6:136844372 | G | GA | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-1232dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136844372 | ||||||
| chr6:136844372 | GA | G | 115 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(112): Show |
125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.340-1232delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 136844372 | ||||||
| chr6:136844577 | A | G | 1 | a0001c0001t0002g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.340-1038A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844577 | |||||||
| chr6:136844614 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.340-1001T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844614 | |||||||
| chr6:136844795 | C | T | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0235 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.340-820C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844795 | |||||||
| chr6:136844808 | A | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-807A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844808 | |||||||
| chr6:136844817 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.340-798C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136844817 | |||||||
| chr6:136845087 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.340-528G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845087 | |||||||
| chr6:136845129 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.340-486T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845129 | |||||||
| chr6:136845333 | G | A | 17 | a0001c0001t0002g0018 a0001c0001t0002g0149 a0001c0001t0002g0185 others(14): Show |
18 | HG00544.hp1 HG01169.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-282G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845333 | |||||||
| chr6:136845507 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.340-108G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845507 | |||||||
| chr6:136845512 | A | G | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-103A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845512 | |||||||
| chr6:136845544 | G | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.340-71G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 3/9 | chr6 | 136845544 | |||||||
| chr6:136845720 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.417+28C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 4/9 | chr6 | 136845720 | |||||||
| chr6:136845839 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.417+147G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 4/9 | chr6 | 136845839 | |||||||
| chr6:136846195 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+14T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846195 | |||||||
| chr6:136846225 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.526+44G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846225 | |||||||
| chr6:136846256 | G | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.526+75G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846256 | |||||||
| chr6:136846287 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+106A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846287 | |||||||
| chr6:136846307 | T | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+126T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846307 | |||||||
| chr6:136846337 | T | C | 1 | a0001c0001t0002g0193 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.526+156T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846337 | |||||||
| chr6:136846338 | A | C | 1 | a0001c0001t0002g0223 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.526+157A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846338 | |||||||
| chr6:136846338 | A | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0094 |
2 | HG01981.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.526+157A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846338 | |||||||
| chr6:136846345 | T | A | 1 | a0001c0001t0002g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526+164T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846345 | |||||||
| chr6:136846388 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.526+207A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846388 | |||||||
| chr6:136846588 | G | A | 4 | a0001c0001t0006g0289 a0001c0001t0006g0290 a0001c0001t0006g0291 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+407G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846588 | |||||||
| chr6:136846589 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.526+408C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846589 | |||||||
| chr6:136846607 | C | G | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.526+426C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846607 | |||||||
| chr6:136846696 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.526+515G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846696 | |||||||
| chr6:136846793 | G | A | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.526+612G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846793 | |||||||
| chr6:136846906 | G | A | 155 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(152): Show |
168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.526+725G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136846906 | |||||||
| chr6:136847026 | T | C | 9 | a0001c0001t0002g0265 a0001c0001t0004g0142 a0001c0001t0004g0143 others(6): Show |
9 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.526+845T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847026 | |||||||
| chr6:136847043 | G | A | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+862G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847043 | |||||||
| chr6:136847120 | GTTGGCTG others(4652): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.526+981_526+5639de others(1): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136847120 | ||||||
| chr6:136847212 | GTT | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.526+1035_526+1036d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136847212 | ||||||
| chr6:136847287 | C | T | 175 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(172): Show |
188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.526+1106C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847287 | |||||||
| chr6:136847342 | A | T | 115 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(112): Show |
125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.526+1161A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847342 | |||||||
| chr6:136847395 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526+1214T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847395 | |||||||
| chr6:136847438 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+1257G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847438 | |||||||
| chr6:136847590 | A | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+1409A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847590 | |||||||
| chr6:136847663 | G | A | 1 | a0001c0001t0005g0119 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.526+1482G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847663 | |||||||
| chr6:136847952 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526+1771C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136847952 | |||||||
| chr6:136848071 | A | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+1890A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848071 | |||||||
| chr6:136848130 | G | T | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+1949G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848130 | |||||||
| chr6:136848143 | T | G | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+1962T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848143 | |||||||
| chr6:136848260 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(2): Show |
6 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+2079T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848260 | |||||||
| chr6:136848290 | A | G | 138 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(135): Show |
150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.526+2109A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848290 | |||||||
| chr6:136848364 | A | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+2183A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848364 | |||||||
| chr6:136848530 | A | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+2349A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848530 | |||||||
| chr6:136848531 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG01081.hp2 HG01123.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.526+2350C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848531 | |||||||
| chr6:136848559 | AG | A | 3 | a0001c0001t0004g0143 a0001c0001t0004g0146 a0002c0002t0004g0147 |
3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.526+2381delG | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136848559 | ||||||
| chr6:136848561 | G | C | 21 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0159 others(18): Show |
23 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.526+2380G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848561 | |||||||
| chr6:136848561 | G | T | 5 | a0001c0001t0002g0021 a0001c0001t0002g0179 a0001c0001t0002g0278 others(2): Show |
6 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+2380G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848561 | |||||||
| chr6:136848663 | T | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+2482T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848663 | |||||||
| chr6:136848710 | T | A | 1 | a0001c0001t0001g0280 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526+2529T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848710 | |||||||
| chr6:136848780 | A | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.526+2599A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848780 | |||||||
| chr6:136848795 | A | G | 26 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0023 others(23): Show |
29 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.526+2614A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848795 | |||||||
| chr6:136848837 | C | G | 1 | a0001c0001t0002g0294 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.526+2656C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848837 | |||||||
| chr6:136848850 | A | G | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+2669A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848850 | |||||||
| chr6:136848888 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526+2707G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136848888 | |||||||
| chr6:136849010 | T | A | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.526+2829T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849010 | |||||||
| chr6:136849013 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0002g0126 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.526+2832T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849013 | |||||||
| chr6:136849168 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.526+2987G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849168 | |||||||
| chr6:136849172 | T | G | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.526+2991T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849172 | |||||||
| chr6:136849324 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.526+3143T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849324 | |||||||
| chr6:136849331 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+3150G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849331 | |||||||
| chr6:136849352 | T | C | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0008g0123 |
3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.526+3171T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849352 | |||||||
| chr6:136849468 | C | T | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.526+3287C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849468 | |||||||
| chr6:136849494 | C | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0296 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.526+3313C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849494 | |||||||
| chr6:136849510 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.526+3329A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849510 | |||||||
| chr6:136849618 | G | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.526+3437G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849618 | |||||||
| chr6:136849870 | T | C | 186 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(183): Show |
199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.526+3689T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136849870 | |||||||
| chr6:136850026 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.526+3845T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850026 | |||||||
| chr6:136850064 | T | G | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.526+3883T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850064 | |||||||
| chr6:136850184 | C | CT | 10 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0004g0142 others(7): Show |
10 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+4013dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850184 | ||||||
| chr6:136850195 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.526+4014G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850195 | |||||||
| chr6:136850233 | A | G | 1 | a0001c0001t0002g0276 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.526+4052A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850233 | |||||||
| chr6:136850268 | G | A | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.526+4087G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850268 | |||||||
| chr6:136850293 | G | C | 20 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0140 others(17): Show |
20 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.526+4112G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850293 | |||||||
| chr6:136850455 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0232 |
2 | HG02083.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.526+4274G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850455 | |||||||
| chr6:136850488 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.526+4307G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850488 | |||||||
| chr6:136850497 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.526+4316C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850497 | |||||||
| chr6:136850603 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.526+4422C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850603 | |||||||
| chr6:136850640 | G | C | 1 | a0001c0001t0002g0253 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.526+4459G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850640 | |||||||
| chr6:136850741 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.526+4560G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850741 | |||||||
| chr6:136850742 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.526+4561C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850742 | |||||||
| chr6:136850833 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.526+4652A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850833 | |||||||
| chr6:136850917 | G | GT | 29 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(26): Show |
33 | HG00140.hp1 HG00544.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.526+4757dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | ||||||
| chr6:136850917 | G | GTT | 30 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0156 others(27): Show |
30 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.526+4756_526+4757d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | ||||||
| chr6:136850917 | G | GTTT | 11 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0155 others(8): Show |
11 | HG01255.hp1 HG01258.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+4755_526+4757d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | ||||||
| chr6:136850917 | GT | G | 51 | a0001c0001t0001g0050 a0001c0001t0001g0066 a0001c0001t0001g0067 others(48): Show |
56 | HG00423.hp1 HG00438.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.526+4757delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | ||||||
| chr6:136850917 | GTT | G | 80 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(77): Show |
85 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.526+4756_526+4757d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | ||||||
| chr6:136850917 | GTTT | G | 10 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0175 others(7): Show |
10 | HG00099.hp1 HG01169.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.526+4755_526+4757d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850917 | ||||||
| chr6:136850927 | T | TG | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+4746_526+4747i others(3): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850927 | |||||||
| chr6:136850969 | CT | C | 13 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0172 others(10): Show |
13 | HG00558.hp2 HG02027.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.526+4798delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850969 | ||||||
| chr6:136850979 | T | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+4798T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136850979 | |||||||
| chr6:136850980 | AT | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(4): Show |
8 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+4809delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850980 | ||||||
| chr6:136850998 | A | AT | 138 | a0001c0001t0001g0153 a0001c0001t0001g0180 a0001c0001t0002g0002 others(135): Show |
149 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.526+4831dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850998 | ||||||
| chr6:136850998 | A | ATT | 6 | a0001c0001t0001g0152 a0001c0001t0002g0140 a0001c0001t0002g0141 others(3): Show |
6 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.526+4830_526+4831d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850998 | ||||||
| chr6:136850998 | AT | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0050 others(10): Show |
14 | HG02155.hp2 HG03139.hp1 HG03516.hp2 others(11): Show |
intron_variant | MODIFIER | c.526+4831delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136850998 | ||||||
| chr6:136851149 | C | A | 12 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+4968C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851149 | |||||||
| chr6:136851221 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.526+5040A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851221 | |||||||
| chr6:136851335 | A | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0248 |
3 | HG01433.hp2 HG03654.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.526+5154A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851335 | |||||||
| chr6:136851365 | G | T | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+5184G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851365 | |||||||
| chr6:136851435 | A | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0210 |
3 | HG00140.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.526+5254A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851435 | |||||||
| chr6:136851450 | G | A | 1 | a0001c0001t0002g0249 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.526+5269G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851450 | |||||||
| chr6:136851570 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0002g0185 others(1): Show |
4 | HG02572.hp1 NA18956.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+5389T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851570 | |||||||
| chr6:136851582 | T | A | 1 | a0001c0001t0005g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.526+5401T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851582 | |||||||
| chr6:136851755 | T | A | 1 | a0001c0001t0001g0004 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.526+5574T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851755 | |||||||
| chr6:136851784 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.526+5603C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851784 | |||||||
| chr6:136851874 | T | G | 7 | a0001c0001t0001g0090 a0001c0001t0002g0236 a0001c0001t0003g0110 others(4): Show |
7 | HG00642.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+5693T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851874 | |||||||
| chr6:136851883 | T | C | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+5702T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851883 | |||||||
| chr6:136851895 | A | T | 1 | a0001c0001t0002g0211 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.526+5714A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851895 | |||||||
| chr6:136851942 | G | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+5761G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851942 | |||||||
| chr6:136851944 | T | C | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+5763T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851944 | |||||||
| chr6:136851945 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+5764G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851945 | |||||||
| chr6:136851998 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.526+5817G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136851998 | |||||||
| chr6:136852000 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+5819G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852000 | |||||||
| chr6:136852040 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0075 others(5): Show |
10 | NA18949.hp2 NA18960.hp1 NA18973.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+5859C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852040 | |||||||
| chr6:136852060 | G | A | 204 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(201): Show |
221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.526+5879G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852060 | |||||||
| chr6:136852083 | G | A | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.526+5902G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852083 | |||||||
| chr6:136852180 | A | G | 1 | a0001c0001t0004g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526+5999A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852180 | |||||||
| chr6:136852388 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.526+6207C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852388 | |||||||
| chr6:136852497 | G | A | 12 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.526+6316G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852497 | |||||||
| chr6:136852506 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+6325T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852506 | |||||||
| chr6:136852560 | A | G | 15 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0106 others(12): Show |
15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.526+6379A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852560 | |||||||
| chr6:136852714 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.526+6533T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852714 | |||||||
| chr6:136852891 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.526+6710C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852891 | |||||||
| chr6:136852892 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.526+6711A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852892 | |||||||
| chr6:136852930 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.526+6749C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852930 | |||||||
| chr6:136852965 | A | C | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+6784A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136852965 | |||||||
| chr6:136853006 | A | G | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+6825A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853006 | |||||||
| chr6:136853121 | A | G | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+6940A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853121 | |||||||
| chr6:136853284 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+7103C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853284 | |||||||
| chr6:136853407 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+7226G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853407 | |||||||
| chr6:136853416 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.526+7235C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853416 | |||||||
| chr6:136853474 | C | CT | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+7294dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136853474 | ||||||
| chr6:136853567 | C | T | 138 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(135): Show |
150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.526+7386C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136853567 | |||||||
| chr6:136854017 | T | C | 4 | a0001c0001t0002g0188 a0001c0001t0002g0199 a0001c0001t0002g0224 others(1): Show |
4 | HG01952.hp2 HG02004.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+7836T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854017 | |||||||
| chr6:136854080 | CTTTACGG others(3): Show |
C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.526+7900_526+7909d others(12): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854080 | |||||||
| chr6:136854133 | A | G | 11 | a0001c0001t0002g0139 a0001c0001t0002g0181 a0001c0001t0002g0182 others(8): Show |
11 | HG02015.hp2 HG02083.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+7952A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854133 | |||||||
| chr6:136854220 | A | G | 3 | a0001c0001t0004g0143 a0001c0001t0004g0146 a0002c0002t0004g0147 |
3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.526+8039A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854220 | |||||||
| chr6:136854344 | A | G | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+8163A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854344 | |||||||
| chr6:136854603 | G | A | 1 | a0001c0001t0010g0262 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.526+8422G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854603 | |||||||
| chr6:136854626 | A | G | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+8445A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854626 | |||||||
| chr6:136854643 | C | T | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(5): Show |
8 | HG02027.hp1 HG03490.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+8462C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854643 | |||||||
| chr6:136854677 | T | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+8496T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854677 | |||||||
| chr6:136854756 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526+8575C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854756 | |||||||
| chr6:136854947 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.526+8766G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854947 | |||||||
| chr6:136854952 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.526+8771G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854952 | |||||||
| chr6:136854993 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
8 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+8812C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854993 | |||||||
| chr6:136854995 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.526+8814G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136854995 | |||||||
| chr6:136855051 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526+8870G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855051 | |||||||
| chr6:136855085 | C | CA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0210 a0001c0001t0004g0143 others(2): Show |
6 | HG00140.hp1 HG01255.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.526+8917dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136855085 | ||||||
| chr6:136855210 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.526+9029A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855210 | |||||||
| chr6:136855347 | C | CT | 36 | a0001c0001t0001g0054 a0001c0001t0001g0092 a0001c0001t0001g0152 others(33): Show |
37 | HG00639.hp2 HG01081.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.526+9180dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136855347 | ||||||
| chr6:136855405 | T | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.526+9224T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855405 | |||||||
| chr6:136855427 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.526+9246C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855427 | |||||||
| chr6:136855582 | C | T | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.526+9401C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855582 | |||||||
| chr6:136855746 | C | T | 110 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(107): Show |
120 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.526+9565C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855746 | |||||||
| chr6:136855836 | T | C | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.526+9655T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855836 | |||||||
| chr6:136855981 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 |
3 | HG03130.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.526+9800C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136855981 | |||||||
| chr6:136856034 | A | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.526+9853A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856034 | |||||||
| chr6:136856291 | T | TA | 27 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0001t0001g0082 others(24): Show |
28 | HG00544.hp2 HG01123.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.526+10136dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856291 | ||||||
| chr6:136856291 | TA | T | 37 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0044 others(34): Show |
39 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.526+10136delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856291 | ||||||
| chr6:136856465 | A | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-10162A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856465 | |||||||
| chr6:136856562 | G | GT | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-10062dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856562 | ||||||
| chr6:136856793 | C | T | 1 | a0001c0001t0002g0292 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.527-9834C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856793 | |||||||
| chr6:136856908 | A | G | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-9719A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136856908 | |||||||
| chr6:136856910 | A | ACAGTAAA others(333): Show |
1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.527-9702_527-9701i others(342): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856910 | ||||||
| chr6:136856910 | A | ACAGTAAA others(350): Show |
1 | a0001c0001t0001g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.527-9702_527-9701i others(359): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136856910 | ||||||
| chr6:136857050 | T | C | 1 | a0001c0001t0002g0292 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.527-9577T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857050 | |||||||
| chr6:136857316 | A | T | 210 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(207): Show |
228 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.527-9311A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857316 | |||||||
| chr6:136857482 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.527-9145C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857482 | |||||||
| chr6:136857686 | CT | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8939delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136857686 | ||||||
| chr6:136857705 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.527-8922T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857705 | |||||||
| chr6:136857863 | C | A | 5 | a0001c0001t0003g0110 a0001c0001t0003g0111 a0001c0001t0003g0112 others(2): Show |
5 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-8764C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857863 | |||||||
| chr6:136857962 | T | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8665T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136857962 | |||||||
| chr6:136858005 | A | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-8622A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858005 | |||||||
| chr6:136858118 | T | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.527-8509T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858118 | |||||||
| chr6:136858249 | G | A | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8378G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858249 | |||||||
| chr6:136858311 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-8316C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858311 | |||||||
| chr6:136858340 | T | C | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.527-8287T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858340 | |||||||
| chr6:136858471 | A | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-8156A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136858471 | |||||||
| chr6:136859277 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.527-7350G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859277 | |||||||
| chr6:136859517 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.527-7110G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859517 | |||||||
| chr6:136859552 | G | C | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.527-7075G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859552 | |||||||
| chr6:136859617 | T | C | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-7010T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859617 | |||||||
| chr6:136859938 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.527-6689C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859938 | |||||||
| chr6:136859948 | C | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.527-6679C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859948 | |||||||
| chr6:136859976 | A | C | 1 | a0001c0001t0001g0045 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.527-6651A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136859976 | |||||||
| chr6:136860014 | G | GA | 11 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(8): Show |
11 | HG02027.hp1 HG02129.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-6600dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860014 | ||||||
| chr6:136860200 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.527-6427T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860200 | |||||||
| chr6:136860276 | C | T | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0008g0123 |
3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.527-6351C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860276 | |||||||
| chr6:136860285 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.527-6342A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860285 | |||||||
| chr6:136860409 | C | CT | 76 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0038 others(73): Show |
82 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.527-6197dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | ||||||
| chr6:136860409 | C | CTT | 7 | a0001c0001t0002g0269 a0001c0001t0004g0143 a0001c0001t0004g0146 others(4): Show |
7 | HG00639.hp2 HG01255.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-6198_527-6197d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | ||||||
| chr6:136860409 | C | CTTT | 13 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0106 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.527-6199_527-6197d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | ||||||
| chr6:136860409 | CT | C | 13 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0039 others(10): Show |
13 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-6197delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860409 | ||||||
| chr6:136860586 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-6041G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860586 | |||||||
| chr6:136860668 | T | TA | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-5948dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860668 | ||||||
| chr6:136860677 | AAAG | A | 154 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(151): Show |
166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.527-5947_527-5945d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860677 | ||||||
| chr6:136860678 | AAG | A | 22 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.527-5947_527-5946d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136860678 | ||||||
| chr6:136860724 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0002g0126 |
2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.527-5903T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860724 | |||||||
| chr6:136860782 | A | C | 2 | a0001c0001t0004g0121 a0001c0001t0004g0122 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.527-5845A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860782 | |||||||
| chr6:136860891 | C | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-5736C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860891 | |||||||
| chr6:136860905 | C | T | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-5722C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860905 | |||||||
| chr6:136860982 | C | A | 4 | a0001c0001t0002g0024 a0001c0001t0002g0239 a0001c0001t0002g0264 others(1): Show |
5 | HG02056.hp2 NA18612.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-5645C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136860982 | |||||||
| chr6:136861108 | A | C | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0134 others(5): Show |
8 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-5519A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861108 | |||||||
| chr6:136861142 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(4): Show |
8 | HG01891.hp2 HG02015.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-5485C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861142 | |||||||
| chr6:136861143 | G | A | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-5484G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861143 | |||||||
| chr6:136861153 | T | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-5474T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861153 | |||||||
| chr6:136861310 | T | G | 2 | a0001c0001t0002g0215 a0001c0001t0002g0222 |
2 | NA18992.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.527-5317T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861310 | |||||||
| chr6:136861437 | A | G | 2 | a0001c0001t0003g0012 a0001c0001t0003g0118 |
3 | HG02257.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.527-5190A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861437 | |||||||
| chr6:136861457 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.527-5170A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861457 | |||||||
| chr6:136861468 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.527-5159A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861468 | |||||||
| chr6:136861630 | G | A | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-4997G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861630 | |||||||
| chr6:136861661 | C | T | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0235 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.527-4966C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861661 | |||||||
| chr6:136861837 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.527-4790A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136861837 | |||||||
| chr6:136862018 | T | TTTATATA others(32): Show |
1 | a0001c0001t0002g0159 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.527-4595_527-4557d others(41): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862018 | ||||||
| chr6:136862019 | T | TTATATAT others(123): Show |
1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.527-4568_527-4567i others(132): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862019 | ||||||
| chr6:136862019 | T | TTATATAT others(95): Show |
1 | a0001c0001t0001g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.527-4568_527-4567i others(104): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862019 | ||||||
| chr6:136862031 | A | ATATT | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0134 others(5): Show |
8 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-4595_527-4594i others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862031 | ||||||
| chr6:136862034 | T | A | 8 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0134 others(5): Show |
8 | HG02027.hp1 HG03710.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.527-4593T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862034 | |||||||
| chr6:136862034 | TTATATAT others(8): Show |
T | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-4571_527-4557d others(17): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136862034 | ||||||
| chr6:136862081 | T | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-4546T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862081 | |||||||
| chr6:136862133 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.527-4494C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862133 | |||||||
| chr6:136862198 | C | T | 1 | a0001c0001t0002g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.527-4429C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862198 | |||||||
| chr6:136862266 | CA | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.527-4360delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862266 | |||||||
| chr6:136862469 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-4158G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862469 | |||||||
| chr6:136862511 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.527-4116G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862511 | |||||||
| chr6:136862801 | T | C | 1 | a0001c0001t0002g0048 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.527-3826T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862801 | |||||||
| chr6:136862847 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.527-3780G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862847 | |||||||
| chr6:136862935 | G | A | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-3692G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136862935 | |||||||
| chr6:136863070 | G | C | 1 | a0001c0001t0002g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.527-3557G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863070 | |||||||
| chr6:136863313 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.527-3314A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863313 | |||||||
| chr6:136863352 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.527-3275T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863352 | |||||||
| chr6:136863354 | G | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.527-3273G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863354 | |||||||
| chr6:136863462 | G | A | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-3165G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863462 | |||||||
| chr6:136863488 | T | C | 12 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.527-3139T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863488 | |||||||
| chr6:136863522 | T | C | 183 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(180): Show |
196 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.527-3105T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863522 | |||||||
| chr6:136863678 | C | G | 2 | a0001c0001t0002g0213 a0001c0001t0004g0144 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.527-2949C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863678 | |||||||
| chr6:136863781 | C | T | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0271 |
3 | HG02132.hp2 NA18946.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.527-2846C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863781 | |||||||
| chr6:136863792 | G | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-2835G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863792 | |||||||
| chr6:136863805 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.527-2822A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863805 | |||||||
| chr6:136863877 | C | G | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(16): Show |
23 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.527-2750C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136863877 | |||||||
| chr6:136864004 | A | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-2623A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864004 | |||||||
| chr6:136864026 | G | A | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-2601G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864026 | |||||||
| chr6:136864155 | A | G | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.527-2472A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864155 | |||||||
| chr6:136864178 | G | T | 1 | a0001c0001t0001g0005 | 3 | HG02027.hp2 NA19011.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.527-2449G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864178 | |||||||
| chr6:136864216 | A | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-2411A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864216 | |||||||
| chr6:136864240 | C | CAAT | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-2385_527-2384i others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136864240 | ||||||
| chr6:136864315 | TA | T | 67 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(64): Show |
70 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.527-2302delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136864315 | ||||||
| chr6:136864315 | TAA | T | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.527-2303_527-2302d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr6 | 136864315 | ||||||
| chr6:136864604 | A | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-2023A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864604 | |||||||
| chr6:136864671 | A | G | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.527-1956A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864671 | |||||||
| chr6:136864697 | A | T | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.527-1930A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864697 | |||||||
| chr6:136864853 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0072 |
3 | HG01074.hp2 HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.527-1774C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864853 | |||||||
| chr6:136864956 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.527-1671T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136864956 | |||||||
| chr6:136865251 | G | C | 1 | a0001c0001t0006g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.527-1376G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865251 | |||||||
| chr6:136865299 | T | C | 1 | a0001c0001t0004g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.527-1328T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865299 | |||||||
| chr6:136865448 | G | A | 1 | a0001c0001t0004g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.527-1179G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865448 | |||||||
| chr6:136865521 | A | G | 3 | a0001c0001t0004g0143 a0001c0001t0004g0146 a0002c0002t0004g0147 |
3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.527-1106A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865521 | |||||||
| chr6:136865592 | C | G | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.527-1035C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865592 | |||||||
| chr6:136865614 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.527-1013C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865614 | |||||||
| chr6:136865757 | A | G | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.527-870A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865757 | |||||||
| chr6:136865777 | C | A | 1 | a0001c0001t0002g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.527-850C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865777 | |||||||
| chr6:136865794 | A | G | 6 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(3): Show |
6 | HG01255.hp2 HG01981.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.527-833A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865794 | |||||||
| chr6:136865807 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527-820G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865807 | |||||||
| chr6:136865811 | G | A | 10 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.527-816G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865811 | |||||||
| chr6:136865953 | T | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-674T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136865953 | |||||||
| chr6:136866000 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-627C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866000 | |||||||
| chr6:136866082 | G | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.527-545G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866082 | |||||||
| chr6:136866096 | A | C | 3 | a0001c0001t0004g0143 a0001c0001t0004g0146 a0002c0002t0004g0147 |
3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.527-531A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866096 | |||||||
| chr6:136866120 | A | T | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.527-507A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866120 | |||||||
| chr6:136866121 | T | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-506T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866121 | |||||||
| chr6:136866438 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.527-189G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866438 | |||||||
| chr6:136866468 | T | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.527-159T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866468 | |||||||
| chr6:136866503 | G | A | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.527-124G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866503 | |||||||
| chr6:136866530 | G | T | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.527-97G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 5/9 | chr6 | 136866530 | |||||||
| chr6:136866822 | G | A | 1 | a0001c0001t0001g0003 | 3 | HG03834.hp2 NA18955.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.633+89G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136866822 | |||||||
| chr6:136867272 | T | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+539T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867272 | |||||||
| chr6:136867285 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.633+552C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867285 | |||||||
| chr6:136867288 | T | C | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+555T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867288 | |||||||
| chr6:136867340 | G | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0167 |
3 | HG01261.hp2 HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.633+607G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867340 | |||||||
| chr6:136867422 | A | G | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.633+689A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867422 | |||||||
| chr6:136867458 | A | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.633+725A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867458 | |||||||
| chr6:136867471 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.633+738C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867471 | |||||||
| chr6:136867597 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.633+864G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867597 | |||||||
| chr6:136867650 | C | T | 10 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0126 others(7): Show |
10 | HG02027.hp1 HG02886.hp1 HG03490.hp1 others(7): Show |
intron_variant | MODIFIER | c.633+917C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867650 | |||||||
| chr6:136867675 | G | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.633+942G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867675 | |||||||
| chr6:136867777 | AAAC | A | 156 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(153): Show |
169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.633+1065_633+1067d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 136867777 | ||||||
| chr6:136867798 | C | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0177 |
3 | HG03098.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.633+1065C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867798 | |||||||
| chr6:136867798 | C | CAAA | 16 | a0001c0001t0001g0038 a0001c0001t0001g0124 a0001c0001t0001g0127 others(13): Show |
20 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.633+1069_633+1071d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr6 | 136867798 | ||||||
| chr6:136867909 | G | T | 1 | a0001c0001t0002g0159 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.633+1176G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867909 | |||||||
| chr6:136867969 | CCA | C | 15 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0106 others(12): Show |
15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.633+1237_633+1238d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867969 | |||||||
| chr6:136867977 | G | A | 1 | a0001c0001t0006g0295 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.633+1244G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136867977 | |||||||
| chr6:136868085 | C | T | 1 | a0001c0001t0008g0123 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.633+1352C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868085 | |||||||
| chr6:136868173 | C | G | 28 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(25): Show |
30 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.633+1440C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868173 | |||||||
| chr6:136868420 | T | C | 3 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | HG02040.hp2 NA18998.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.634-1470T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868420 | |||||||
| chr6:136868442 | T | C | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.634-1448T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868442 | |||||||
| chr6:136868841 | G | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.634-1049G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868841 | |||||||
| chr6:136868911 | G | C | 17 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0140 others(14): Show |
17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.634-979G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136868911 | |||||||
| chr6:136869070 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.634-820C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869070 | |||||||
| chr6:136869272 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.634-618C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869272 | |||||||
| chr6:136869703 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.634-187A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869703 | |||||||
| chr6:136869738 | C | T | 17 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0140 others(14): Show |
17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.634-152C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869738 | |||||||
| chr6:136869771 | T | C | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.634-119T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869771 | |||||||
| chr6:136869816 | T | C | 1 | a0001c0001t0003g0012 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.634-74T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 6/9 | chr6 | 136869816 | |||||||
| chr6:136870262 | A | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.747+259A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870262 | |||||||
| chr6:136870616 | T | C | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+613T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870616 | |||||||
| chr6:136870687 | C | G | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(19): Show |
24 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.747+684C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870687 | |||||||
| chr6:136870832 | G | A | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.747+829G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136870832 | |||||||
| chr6:136871027 | A | G | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.747+1024A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871027 | |||||||
| chr6:136871312 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.748-886T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871312 | |||||||
| chr6:136871390 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.748-808G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871390 | |||||||
| chr6:136871684 | C | G | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.748-514C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | chr6 | 136871684 | |||||||
| chr6:136871992 | A | AAT | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.748-203_748-202dup others(2): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 136871992 | ||||||
| chr6:136872298 | A | G | 25 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0140 others(22): Show |
25 | HG00639.hp2 HG01255.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+45A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872298 | |||||||
| chr6:136872358 | A | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0034 others(7): Show |
11 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+105A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872358 | |||||||
| chr6:136872416 | C | T | 17 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0140 others(14): Show |
17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+163C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872416 | |||||||
| chr6:136872616 | G | T | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+363G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872616 | |||||||
| chr6:136872754 | T | G | 2 | a0001c0001t0002g0204 a0001c0001t0002g0241 |
2 | HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.803+501T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872754 | |||||||
| chr6:136872895 | T | C | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+642T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872895 | |||||||
| chr6:136872950 | T | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+697T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136872950 | |||||||
| chr6:136873001 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+748C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873001 | |||||||
| chr6:136873232 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.803+979T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873232 | |||||||
| chr6:136873388 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.803+1135T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873388 | |||||||
| chr6:136873584 | G | A | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+1331G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873584 | |||||||
| chr6:136873629 | C | G | 1 | a0001c0001t0002g0292 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.803+1376C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873629 | |||||||
| chr6:136873696 | G | T | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0008g0123 |
3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+1443G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873696 | |||||||
| chr6:136873719 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.803+1466T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873719 | |||||||
| chr6:136873859 | C | G | 1 | a0001c0001t0002g0288 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.803+1606C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136873859 | |||||||
| chr6:136874044 | G | A | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(23): Show |
28 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.803+1791G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874044 | |||||||
| chr6:136874076 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.803+1823T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874076 | |||||||
| chr6:136874138 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+1885G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874138 | |||||||
| chr6:136874236 | G | C | 2 | a0001c0001t0002g0125 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.803+1983G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874236 | |||||||
| chr6:136874320 | C | T | 159 | a0001c0001t0001g0124 a0001c0001t0001g0152 a0001c0001t0001g0153 others(156): Show |
170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.803+2067C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874320 | |||||||
| chr6:136874400 | A | T | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.803+2147A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874400 | |||||||
| chr6:136874438 | A | C | 1 | a0001c0001t0002g0268 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.803+2185A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874438 | |||||||
| chr6:136874530 | C | G | 158 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0180 others(155): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.803+2277C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874530 | |||||||
| chr6:136874656 | G | A | 1 | a0001c0001t0008g0123 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.803+2403G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874656 | |||||||
| chr6:136874668 | C | CA | 15 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(12): Show |
15 | HG00423.hp1 HG00438.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.803+2435dupA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136874668 | ||||||
| chr6:136874668 | CA | C | 8 | a0001c0001t0001g0053 a0001c0001t0001g0170 a0001c0001t0001g0180 others(5): Show |
8 | HG00609.hp2 HG00639.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+2435delA | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136874668 | ||||||
| chr6:136874693 | A | C | 1 | a0001c0001t0002g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.803+2440A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874693 | |||||||
| chr6:136874807 | T | C | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+2554T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874807 | |||||||
| chr6:136874846 | A | T | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+2593A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136874846 | |||||||
| chr6:136875006 | G | T | 15 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0106 others(12): Show |
15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+2753G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875006 | |||||||
| chr6:136875094 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0097 |
2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.803+2841G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875094 | |||||||
| chr6:136875159 | C | CT | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+2917dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136875159 | ||||||
| chr6:136875230 | T | C | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+2977T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875230 | |||||||
| chr6:136875277 | T | TTAA | 158 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0180 others(155): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.803+3025_803+3027d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136875277 | ||||||
| chr6:136875362 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.803+3109A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875362 | |||||||
| chr6:136875511 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.803+3258T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875511 | |||||||
| chr6:136875557 | G | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+3304G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875557 | |||||||
| chr6:136875786 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803+3533A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875786 | |||||||
| chr6:136875850 | G | C | 1 | a0001c0001t0005g0119 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.803+3597G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875850 | |||||||
| chr6:136875888 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.803+3635A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875888 | |||||||
| chr6:136875957 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.803+3704C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136875957 | |||||||
| chr6:136876042 | AT | A | 175 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0030 others(172): Show |
192 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.803+3802delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136876042 | ||||||
| chr6:136876261 | TCTC | T | 12 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0003g0007 others(9): Show |
16 | HG02257.hp2 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.803+4011_803+4013d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136876261 | ||||||
| chr6:136876272 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.803+4019C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876272 | |||||||
| chr6:136876583 | C | T | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.803+4330C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876583 | |||||||
| chr6:136876605 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.803+4352C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876605 | |||||||
| chr6:136876667 | C | T | 1 | a0001c0001t0002g0255 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.803+4414C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876667 | |||||||
| chr6:136876729 | A | G | 12 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+4476A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876729 | |||||||
| chr6:136876875 | A | G | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+4622A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136876875 | |||||||
| chr6:136877075 | T | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0041 others(8): Show |
12 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+4822T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877075 | |||||||
| chr6:136877150 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803+4897A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877150 | |||||||
| chr6:136877461 | T | C | 1 | a0001c0001t0002g0278 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.803+5208T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877461 | |||||||
| chr6:136877912 | G | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+5659G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136877912 | |||||||
| chr6:136878212 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.803+5959G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878212 | |||||||
| chr6:136878217 | G | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+5964G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878217 | |||||||
| chr6:136878257 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.803+6004C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878257 | |||||||
| chr6:136878397 | A | G | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+6144A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878397 | |||||||
| chr6:136878413 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.803+6160C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878413 | |||||||
| chr6:136878589 | A | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0179 a0001c0001t0002g0282 others(1): Show |
5 | HG01106.hp1 HG01192.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+6336A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878589 | |||||||
| chr6:136878642 | A | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6389A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878642 | |||||||
| chr6:136878683 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.803+6430A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878683 | |||||||
| chr6:136878704 | C | T | 15 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0106 others(12): Show |
15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+6451C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878704 | |||||||
| chr6:136878878 | C | CTT | 150 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0180 others(147): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.803+6625_803+6626i others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136878878 | |||||||
| chr6:136879028 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803+6775C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879028 | |||||||
| chr6:136879052 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6799G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879052 | |||||||
| chr6:136879081 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6828C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879081 | |||||||
| chr6:136879084 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6831T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879084 | |||||||
| chr6:136879088 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803+6835C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879088 | |||||||
| chr6:136879167 | A | T | 15 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0106 others(12): Show |
15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+6914A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879167 | |||||||
| chr6:136879289 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803+7036T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879289 | |||||||
| chr6:136879598 | T | G | 1 | a0001c0001t0004g0143 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803+7345T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879598 | |||||||
| chr6:136879685 | A | C | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+7432A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879685 | |||||||
| chr6:136879707 | A | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0219 |
2 | HG01169.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.803+7454A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879707 | |||||||
| chr6:136879882 | A | C | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+7629A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136879882 | |||||||
| chr6:136880126 | T | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+7873T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880126 | |||||||
| chr6:136880140 | G | C | 1 | a0001c0001t0002g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803+7887G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880140 | |||||||
| chr6:136880287 | A | G | 1 | a0001c0001t0002g0264 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.803+8034A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880287 | |||||||
| chr6:136880791 | T | A | 1 | a0001c0001t0002g0243 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.803+8538T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880791 | |||||||
| chr6:136880861 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+8608G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880861 | |||||||
| chr6:136880971 | A | G | 1 | a0001c0001t0002g0048 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.803+8718A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880971 | |||||||
| chr6:136880974 | A | G | 3 | a0001c0001t0004g0143 a0001c0001t0004g0146 a0002c0002t0004g0147 |
3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.803+8721A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136880974 | |||||||
| chr6:136881140 | T | C | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.803+8887T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136881140 | |||||||
| chr6:136881367 | C | T | 10 | a0001c0001t0001g0180 a0001c0001t0002g0017 a0001c0001t0002g0126 others(7): Show |
11 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.803+9114C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136881367 | |||||||
| chr6:136881965 | C | G | 10 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.803+9712C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136881965 | |||||||
| chr6:136882058 | A | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+9805A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882058 | |||||||
| chr6:136882078 | T | C | 2 | a0001c0001t0003g0013 a0001c0001t0003g0115 |
3 | HG02647.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.803+9825T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882078 | |||||||
| chr6:136882093 | A | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 |
3 | NA18955.hp1 NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.803+9840A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882093 | |||||||
| chr6:136882175 | C | CT | 58 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(55): Show |
66 | HG00323.hp2 HG00558.hp2 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.803+9944dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882175 | ||||||
| chr6:136882175 | C | CTT | 7 | a0001c0001t0001g0052 a0001c0001t0001g0124 a0001c0001t0001g0157 others(4): Show |
7 | HG00423.hp2 HG00597.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+9943_803+9944d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882175 | ||||||
| chr6:136882175 | CT | C | 24 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0075 others(21): Show |
24 | HG01255.hp2 HG01981.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.803+9944delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882175 | ||||||
| chr6:136882177 | T | TC | 3 | a0001c0001t0001g0038 a0001c0001t0002g0176 a0001c0001t0002g0296 |
3 | HG02630.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.803+9924_803+9925i others(3): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882177 | |||||||
| chr6:136882178 | T | C | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0094 others(6): Show |
10 | HG01358.hp1 HG01981.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.803+9925T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882178 | |||||||
| chr6:136882346 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.803+10093C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882346 | |||||||
| chr6:136882548 | A | AAAT | 132 | a0001c0001t0001g0180 a0001c0001t0002g0002 a0001c0001t0002g0017 others(129): Show |
143 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.803+10314_803+1031 others(7): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136882548 | ||||||
| chr6:136882608 | G | A | 176 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(173): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.803+10355G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882608 | |||||||
| chr6:136882692 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.803+10439G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882692 | |||||||
| chr6:136882719 | C | T | 2 | a0001c0001t0002g0149 a0001c0001t0002g0206 |
2 | HG02056.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.803+10466C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882719 | |||||||
| chr6:136882769 | A | G | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+10516A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882769 | |||||||
| chr6:136882877 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803+10624C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882877 | |||||||
| chr6:136882878 | G | C | 161 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0180 others(158): Show |
172 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.803+10625G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882878 | |||||||
| chr6:136882880 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+10627A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882880 | |||||||
| chr6:136882928 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.803+10675G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136882928 | |||||||
| chr6:136883038 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.803+10785G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883038 | |||||||
| chr6:136883142 | C | T | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.803+10889C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883142 | |||||||
| chr6:136883184 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.803+10931C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883184 | |||||||
| chr6:136883420 | T | G | 11 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(8): Show |
11 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+11167T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883420 | |||||||
| chr6:136883453 | C | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.803+11200C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883453 | |||||||
| chr6:136883497 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.803+11244A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883497 | |||||||
| chr6:136883501 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.803+11248T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883501 | |||||||
| chr6:136883597 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.803+11344C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883597 | |||||||
| chr6:136883692 | C | T | 17 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0140 others(14): Show |
17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+11439C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883692 | |||||||
| chr6:136883740 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+11487G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883740 | |||||||
| chr6:136883741 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.803+11488G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883741 | |||||||
| chr6:136883960 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.803+11707G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136883960 | |||||||
| chr6:136884042 | C | T | 3 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 |
3 | NA18955.hp1 NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.803+11789C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884042 | |||||||
| chr6:136884070 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.803+11817A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884070 | |||||||
| chr6:136884230 | G | A | 17 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0140 others(14): Show |
17 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+11977G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884230 | |||||||
| chr6:136884357 | C | G | 2 | a0001c0001t0002g0205 a0001c0001t0002g0242 |
2 | NA19007.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.803+12104C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884357 | |||||||
| chr6:136884505 | A | G | 1 | a0001c0001t0002g0017 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.803+12252A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884505 | |||||||
| chr6:136884513 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.803+12260A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884513 | |||||||
| chr6:136884626 | TTTGAAA | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+12376_803+1238 others(10): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136884626 | ||||||
| chr6:136884635 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+12382C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884635 | |||||||
| chr6:136884834 | T | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+12581T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884834 | |||||||
| chr6:136884943 | C | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0274 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.803+12690C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884943 | |||||||
| chr6:136884944 | G | A | 3 | a0001c0001t0004g0143 a0001c0001t0004g0146 a0002c0002t0004g0147 |
3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.803+12691G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136884944 | |||||||
| chr6:136885124 | A | G | 184 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0152 others(181): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.803+12871A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885124 | |||||||
| chr6:136885187 | A | G | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.803+12934A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885187 | |||||||
| chr6:136885436 | G | A | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0296 |
3 | HG02109.hp1 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.804-12706G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885436 | |||||||
| chr6:136885790 | A | G | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.804-12352A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885790 | |||||||
| chr6:136885793 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.804-12349G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136885793 | |||||||
| chr6:136886166 | G | A | 114 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(111): Show |
124 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.804-11976G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886166 | |||||||
| chr6:136886293 | A | T | 1 | a0001c0001t0006g0295 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.804-11849A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886293 | |||||||
| chr6:136886435 | A | G | 1 | a0001c0001t0008g0123 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804-11707A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886435 | |||||||
| chr6:136886551 | G | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.804-11591G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136886551 | |||||||
| chr6:136886735 | ATGTC | A | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.804-11404_804-1140 others(8): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136886735 | ||||||
| chr6:136887489 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.804-10653A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136887489 | |||||||
| chr6:136887600 | A | G | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-10542A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136887600 | |||||||
| chr6:136887625 | TAAAAC | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(20): Show |
25 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.804-10513_804-1050 others(9): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136887625 | ||||||
| chr6:136887854 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.804-10288T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136887854 | |||||||
| chr6:136888141 | C | T | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.804-10001C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888141 | |||||||
| chr6:136888173 | G | C | 156 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(153): Show |
167 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.804-9969G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888173 | |||||||
| chr6:136888453 | A | G | 46 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0022 others(43): Show |
52 | HG00323.hp1 HG00438.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.804-9689A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888453 | |||||||
| chr6:136888570 | G | A | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-9572G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888570 | |||||||
| chr6:136888579 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.804-9563A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888579 | |||||||
| chr6:136888695 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.804-9447A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888695 | |||||||
| chr6:136888720 | A | T | 15 | a0001c0001t0002g0022 a0001c0001t0002g0192 a0001c0001t0002g0193 others(12): Show |
16 | HG02074.hp1 NA18944.hp1 NA18949.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-9422A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888720 | |||||||
| chr6:136888795 | T | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-9347T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888795 | |||||||
| chr6:136888804 | G | A | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0235 |
3 | HG02922.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.804-9338G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888804 | |||||||
| chr6:136888903 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(17): Show |
21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-9239T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136888903 | |||||||
| chr6:136889391 | C | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.804-8751C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889391 | |||||||
| chr6:136889431 | A | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-8711A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889431 | |||||||
| chr6:136889563 | T | C | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0008g0123 |
3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.804-8579T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889563 | |||||||
| chr6:136889574 | A | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(14): Show |
18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.804-8568A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889574 | |||||||
| chr6:136889806 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.804-8336A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889806 | |||||||
| chr6:136889948 | C | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
8 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-8194C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136889948 | |||||||
| chr6:136890183 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.804-7959C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890183 | |||||||
| chr6:136890257 | A | C | 8 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(5): Show |
8 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-7885A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890257 | |||||||
| chr6:136890350 | C | G | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0154 others(19): Show |
24 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.804-7792C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890350 | |||||||
| chr6:136890391 | A | G | 4 | a0001c0001t0002g0230 a0001c0001t0007g0025 a0001c0001t0007g0026 others(1): Show |
4 | HG03139.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.804-7751A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890391 | |||||||
| chr6:136890416 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-7726C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890416 | |||||||
| chr6:136890435 | C | A | 1 | a0001c0001t0002g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.804-7707C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890435 | |||||||
| chr6:136890514 | G | T | 128 | a0001c0001t0001g0180 a0001c0001t0002g0002 a0001c0001t0002g0018 others(125): Show |
138 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.804-7628G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890514 | |||||||
| chr6:136890785 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.804-7357C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136890785 | |||||||
| chr6:136891038 | G | C | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-7104G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891038 | |||||||
| chr6:136891235 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.804-6907G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891235 | |||||||
| chr6:136891279 | A | G | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.804-6863A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891279 | |||||||
| chr6:136891395 | T | C | 12 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0003g0007 others(9): Show |
16 | HG02257.hp2 HG02572.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.804-6747T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891395 | |||||||
| chr6:136891454 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(14): Show |
18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.804-6688A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891454 | |||||||
| chr6:136891651 | CT | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0080 others(15): Show |
19 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.804-6476delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136891651 | ||||||
| chr6:136891782 | A | C | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.804-6360A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891782 | |||||||
| chr6:136891817 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.804-6325G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891817 | |||||||
| chr6:136891916 | G | A | 1 | a0001c0001t0011g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.804-6226G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891916 | |||||||
| chr6:136891921 | C | T | 2 | a0001c0001t0003g0012 a0001c0001t0003g0118 |
3 | HG02257.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.804-6221C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136891921 | |||||||
| chr6:136892009 | A | G | 3 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | HG02040.hp2 NA18998.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.804-6133A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892009 | |||||||
| chr6:136892037 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.804-6105T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892037 | |||||||
| chr6:136892260 | T | C | 4 | a0001c0001t0002g0287 a0001c0001t0006g0289 a0001c0001t0006g0290 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.804-5882T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892260 | |||||||
| chr6:136892957 | T | A | 6 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(3): Show |
6 | HG01255.hp2 HG01981.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.804-5185T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136892957 | |||||||
| chr6:136893009 | T | C | 182 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(179): Show |
198 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.804-5133T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893009 | |||||||
| chr6:136893068 | C | T | 191 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(188): Show |
208 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.804-5074C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893068 | |||||||
| chr6:136893151 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0074 |
2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.804-4991G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893151 | |||||||
| chr6:136893199 | T | A | 1 | a0001c0001t0002g0232 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.804-4943T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893199 | |||||||
| chr6:136893202 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0015 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.804-4933_804-4932i others(33): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136893202 | ||||||
| chr6:136893268 | T | G | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.804-4874T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893268 | |||||||
| chr6:136893278 | G | C | 1 | a0001c0001t0002g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.804-4864G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893278 | |||||||
| chr6:136893320 | G | T | 1 | a0001c0001t0002g0234 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.804-4822G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893320 | |||||||
| chr6:136893444 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804-4698C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893444 | |||||||
| chr6:136893466 | C | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.804-4676C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893466 | |||||||
| chr6:136893503 | T | A | 9 | a0001c0001t0002g0017 a0001c0001t0002g0126 a0001c0001t0002g0176 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.804-4639T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893503 | |||||||
| chr6:136893549 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.804-4593G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893549 | |||||||
| chr6:136893688 | A | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(17): Show |
21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-4454A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136893688 | |||||||
| chr6:136894023 | G | A | 7 | a0001c0001t0002g0184 a0001c0001t0002g0200 a0001c0001t0002g0240 others(4): Show |
7 | HG02148.hp1 NA18948.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-4119G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894023 | |||||||
| chr6:136894186 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.804-3956C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894186 | |||||||
| chr6:136894218 | G | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.804-3924G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894218 | |||||||
| chr6:136894241 | A | G | 191 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(188): Show |
208 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.804-3901A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894241 | |||||||
| chr6:136894318 | A | T | 1 | a0001c0001t0002g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.804-3824A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894318 | |||||||
| chr6:136894390 | G | A | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-3752G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894390 | |||||||
| chr6:136894393 | C | T | 20 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(17): Show |
21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-3749C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894393 | |||||||
| chr6:136894415 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(17): Show |
21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-3727T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894415 | |||||||
| chr6:136894501 | A | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(17): Show |
21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-3641A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894501 | |||||||
| chr6:136894545 | G | A | 115 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(112): Show |
125 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.804-3597G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894545 | |||||||
| chr6:136894739 | G | A | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-3403G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894739 | |||||||
| chr6:136894928 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(4): Show |
8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-3214A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136894928 | |||||||
| chr6:136895003 | A | T | 2 | a0001c0001t0004g0145 a0001c0001t0008g0028 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.804-3139A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895003 | |||||||
| chr6:136895629 | C | T | 1 | a0001c0001t0003g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.804-2513C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895629 | |||||||
| chr6:136895631 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-2511T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895631 | |||||||
| chr6:136895709 | A | T | 148 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(145): Show |
159 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.804-2433A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895709 | |||||||
| chr6:136895778 | A | G | 1 | a0001c0001t0002g0250 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.804-2364A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895778 | |||||||
| chr6:136895803 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.804-2339C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136895803 | |||||||
| chr6:136895877 | TG | T | 9 | a0001c0001t0002g0017 a0001c0001t0002g0126 a0001c0001t0002g0176 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.804-2263delG | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136895877 | ||||||
| chr6:136896129 | C | T | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-2013C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136896129 | |||||||
| chr6:136896216 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.804-1926A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136896216 | |||||||
| chr6:136896604 | G | GTCCTTCC others(60): Show |
1 | a0001c0001t0002g0260 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.804-1475_804-1474i others(69): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 136896604 | ||||||
| chr6:136896974 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.804-1168T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136896974 | |||||||
| chr6:136897124 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0155 a0001c0001t0001g0156 others(11): Show |
15 | HG00323.hp2 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-1018G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897124 | |||||||
| chr6:136897507 | T | G | 1 | a0001c0001t0009g0151 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.804-635T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897507 | |||||||
| chr6:136897554 | T | C | 117 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(114): Show |
127 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.804-588T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897554 | |||||||
| chr6:136897632 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.804-510A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897632 | |||||||
| chr6:136897696 | A | G | 1 | a0001c0001t0002g0198 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.804-446A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136897696 | |||||||
| chr6:136898096 | T | G | 1 | a0001c0001t0002g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.804-46T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 8/9 | chr6 | 136898096 | |||||||
| chr6:136898294 | C | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(4): Show |
7 | HG02155.hp2 NA18612.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+53C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898294 | |||||||
| chr6:136898462 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.903+221A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898462 | |||||||
| chr6:136898589 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.903+348T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898589 | |||||||
| chr6:136898593 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+352C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898593 | |||||||
| chr6:136898800 | T | C | 9 | a0001c0001t0002g0017 a0001c0001t0002g0126 a0001c0001t0002g0176 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+559T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898800 | |||||||
| chr6:136898819 | T | A | 132 | a0001c0001t0001g0180 a0001c0001t0002g0002 a0001c0001t0002g0018 others(129): Show |
142 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.903+578T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898819 | |||||||
| chr6:136898855 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(14): Show |
18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+614A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136898855 | |||||||
| chr6:136899080 | C | CT | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0166 others(10): Show |
13 | HG01255.hp2 HG01884.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.903+857dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899080 | ||||||
| chr6:136899080 | C | CTT | 112 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0019 others(109): Show |
122 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.903+856_903+857dup others(2): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899080 | ||||||
| chr6:136899080 | CT | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0075 others(4): Show |
9 | NA18949.hp2 NA18960.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+857delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899080 | ||||||
| chr6:136899084 | T | TC | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+843_903+844ins others(1): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899084 | |||||||
| chr6:136899087 | T | TC | 3 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0027 |
3 | HG03139.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.903+846_903+847ins others(1): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899087 | |||||||
| chr6:136899142 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.903+901G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899142 | |||||||
| chr6:136899193 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.903+952A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899193 | |||||||
| chr6:136899197 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.903+956C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899197 | |||||||
| chr6:136899247 | A | AT | 12 | a0001c0001t0001g0180 a0001c0001t0004g0142 a0001c0001t0004g0143 others(9): Show |
12 | HG01255.hp2 HG01981.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+1020dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136899247 | ||||||
| chr6:136899265 | A | C | 9 | a0001c0001t0002g0017 a0001c0001t0002g0126 a0001c0001t0002g0176 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+1024A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899265 | |||||||
| chr6:136899269 | T | C | 2 | a0001c0001t0004g0145 a0001c0001t0008g0028 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.903+1028T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899269 | |||||||
| chr6:136899275 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.903+1034C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899275 | |||||||
| chr6:136899571 | G | A | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.903+1330G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899571 | |||||||
| chr6:136899648 | G | A | 9 | a0001c0001t0002g0017 a0001c0001t0002g0126 a0001c0001t0002g0176 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.903+1407G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899648 | |||||||
| chr6:136899927 | C | G | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.903+1686C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899927 | |||||||
| chr6:136899968 | T | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(14): Show |
18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+1727T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136899968 | |||||||
| chr6:136900104 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.903+1863G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900104 | |||||||
| chr6:136900117 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.903+1876G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900117 | |||||||
| chr6:136900228 | A | T | 1 | a0001c0001t0002g0017 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.903+1987A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900228 | |||||||
| chr6:136900468 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.903+2227C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900468 | |||||||
| chr6:136900690 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.903+2449G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900690 | |||||||
| chr6:136900821 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.903+2580G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900821 | |||||||
| chr6:136900831 | T | A | 4 | a0001c0001t0002g0024 a0001c0001t0002g0239 a0001c0001t0002g0264 others(1): Show |
5 | HG02056.hp2 NA18612.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+2590T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136900831 | |||||||
| chr6:136901093 | T | C | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0008g0123 |
3 | HG02109.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.903+2852T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901093 | |||||||
| chr6:136901152 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+2911C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901152 | |||||||
| chr6:136901249 | T | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(28): Show |
32 | HG00639.hp2 HG01192.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.903+3008T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901249 | |||||||
| chr6:136901453 | G | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(14): Show |
18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+3212G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901453 | |||||||
| chr6:136901533 | A | G | 156 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(153): Show |
167 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.903+3292A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901533 | |||||||
| chr6:136901832 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.903+3591C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901832 | |||||||
| chr6:136901846 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.903+3605C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901846 | |||||||
| chr6:136901974 | G | A | 6 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0001c0001t0004g0145 others(3): Show |
6 | HG01255.hp2 HG01981.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.903+3733G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136901974 | |||||||
| chr6:136902301 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0277 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.903+4060G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902301 | |||||||
| chr6:136902421 | T | C | 1 | a0001c0001t0004g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.903+4180T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902421 | |||||||
| chr6:136902541 | C | T | 2 | a0001c0001t0002g0215 a0001c0001t0002g0222 |
2 | NA18992.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.903+4300C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902541 | |||||||
| chr6:136902637 | T | C | 1 | a0001c0001t0002g0247 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.903+4396T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902637 | |||||||
| chr6:136902729 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.903+4488A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902729 | |||||||
| chr6:136902770 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.903+4529A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136902770 | |||||||
| chr6:136903032 | T | C | 2 | a0001c0001t0005g0116 a0001c0001t0005g0120 |
2 | HG00639.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.903+4791T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903032 | |||||||
| chr6:136903205 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.903+4964A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903205 | |||||||
| chr6:136903336 | C | CT | 116 | a0001c0001t0001g0074 a0001c0001t0001g0086 a0001c0001t0001g0089 others(113): Show |
126 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.903+5114dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136903336 | ||||||
| chr6:136903724 | G | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(17): Show |
21 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.903+5483G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903724 | |||||||
| chr6:136903762 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.903+5521C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903762 | |||||||
| chr6:136903828 | A | C | 1 | a0001c0001t0002g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.903+5587A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903828 | |||||||
| chr6:136903829 | CT | C | 41 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0049 others(38): Show |
43 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.903+5603delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136903829 | ||||||
| chr6:136903863 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+5622G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903863 | |||||||
| chr6:136903908 | G | C | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.903+5667G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136903908 | |||||||
| chr6:136904104 | TAGA | T | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+5867_903+5869d others(5): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136904104 | ||||||
| chr6:136904143 | G | A | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+5902G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904143 | |||||||
| chr6:136904373 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0086 a0001c0001t0001g0174 |
4 | HG00639.hp1 HG01433.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.903+6132T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904373 | |||||||
| chr6:136904444 | T | C | 2 | a0001c0001t0002g0140 a0001c0001t0002g0141 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.903+6203T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904444 | |||||||
| chr6:136904632 | C | CT | 9 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0001t0001g0069 others(6): Show |
9 | HG00544.hp1 HG00597.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.903+6409dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136904632 | ||||||
| chr6:136904632 | CT | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0163 a0001c0001t0002g0017 others(10): Show |
15 | HG00323.hp2 HG01516.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.903+6409delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136904632 | ||||||
| chr6:136904670 | G | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0054 others(2): Show |
5 | NA18953.hp1 NA18969.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+6429G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904670 | |||||||
| chr6:136904678 | A | T | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.903+6437A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904678 | |||||||
| chr6:136904705 | C | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(14): Show |
18 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.903+6464C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904705 | |||||||
| chr6:136904779 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.903+6538T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904779 | |||||||
| chr6:136904783 | A | G | 2 | a0001c0001t0002g0125 a0001c0001t0002g0177 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.903+6542A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904783 | |||||||
| chr6:136904874 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.903+6633C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136904874 | |||||||
| chr6:136905025 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.903+6784G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905025 | |||||||
| chr6:136905133 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.903+6892C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905133 | |||||||
| chr6:136905320 | T | C | 3 | a0001c0001t0004g0143 a0001c0001t0004g0146 a0002c0002t0004g0147 |
3 | HG01255.hp2 HG01981.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.903+7079T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905320 | |||||||
| chr6:136905422 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.903+7181C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905422 | |||||||
| chr6:136905559 | C | T | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+7318C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905559 | |||||||
| chr6:136905695 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.903+7454A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136905695 | |||||||
| chr6:136906051 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0115 |
6 | HG02572.hp1 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-7407C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906051 | |||||||
| chr6:136906137 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.904-7321A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906137 | |||||||
| chr6:136906301 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.904-7157T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906301 | |||||||
| chr6:136906433 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.904-7025C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906433 | |||||||
| chr6:136906534 | G | T | 9 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(6): Show |
9 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-6924G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906534 | |||||||
| chr6:136906749 | C | G | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(16): Show |
23 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.904-6709C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906749 | |||||||
| chr6:136906841 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 |
3 | HG03130.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.904-6617C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906841 | |||||||
| chr6:136906956 | G | A | 180 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(177): Show |
196 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.904-6502G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906956 | |||||||
| chr6:136906962 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.904-6496C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136906962 | |||||||
| chr6:136907159 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0272 |
2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.904-6299C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907159 | |||||||
| chr6:136907213 | C | G | 1 | a0001c0001t0002g0251 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.904-6245C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907213 | |||||||
| chr6:136907496 | TC | T | 25 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0031 others(22): Show |
30 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.904-5961delC | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907496 | |||||||
| chr6:136907509 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.904-5949A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907509 | |||||||
| chr6:136907514 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0279 others(12): Show |
16 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.904-5944T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136907514 | |||||||
| chr6:136908006 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.904-5452G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908006 | |||||||
| chr6:136908105 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.904-5353A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908105 | |||||||
| chr6:136908219 | G | A | 1 | a0001c0001t0002g0263 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.904-5239G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908219 | |||||||
| chr6:136908262 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.904-5196A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908262 | |||||||
| chr6:136908332 | T | A | 1 | a0001c0001t0002g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.904-5126T>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908332 | |||||||
| chr6:136908340 | GT | G | 5 | a0001c0001t0003g0110 a0001c0001t0003g0111 a0001c0001t0003g0112 others(2): Show |
5 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-5110delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136908340 | ||||||
| chr6:136908389 | G | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.904-5069G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908389 | |||||||
| chr6:136908642 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0152 others(4): Show |
8 | HG01192.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-4816A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908642 | |||||||
| chr6:136908676 | CAA | C | 10 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.904-4781_904-4780d others(4): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908676 | |||||||
| chr6:136908721 | A | G | 1 | a0001c0001t0002g0255 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.904-4737A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908721 | |||||||
| chr6:136908764 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(8): Show |
12 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.904-4694A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908764 | |||||||
| chr6:136908823 | G | T | 4 | a0001c0001t0002g0139 a0001c0001t0002g0197 a0001c0001t0002g0249 others(1): Show |
4 | HG03710.hp2 NA18942.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-4635G>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908823 | |||||||
| chr6:136908830 | T | TC | 5 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(2): Show |
6 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-4625dupC | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136908830 | ||||||
| chr6:136908833 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.904-4625C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908833 | |||||||
| chr6:136908870 | CT | C | 3 | a0001c0001t0002g0133 a0001c0001t0002g0139 a0001c0001t0002g0294 |
3 | HG03490.hp1 HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.904-4587delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908870 | |||||||
| chr6:136908903 | G | A | 7 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0002g0125 others(4): Show |
7 | HG02258.hp2 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-4555G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908903 | |||||||
| chr6:136908974 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.904-4484A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136908974 | |||||||
| chr6:136909048 | T | C | 12 | a0001c0001t0001g0124 a0001c0001t0003g0007 a0001c0001t0003g0012 others(9): Show |
16 | HG01255.hp2 HG01981.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.904-4410T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909048 | |||||||
| chr6:136909079 | A | G | 16 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0038 others(13): Show |
16 | HG02145.hp2 HG02572.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.904-4379A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909079 | |||||||
| chr6:136909147 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.904-4311A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909147 | |||||||
| chr6:136909178 | A | G | 1 | a0001c0001t0002g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.904-4280A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909178 | |||||||
| chr6:136909311 | A | AAAAC | 7 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(4): Show |
8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-4135_904-4132d others(6): Show |
PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136909311 | ||||||
| chr6:136909398 | C | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(4): Show |
8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-4060C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909398 | |||||||
| chr6:136909505 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.904-3953G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909505 | |||||||
| chr6:136909511 | A | G | 6 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(3): Show |
6 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-3947A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909511 | |||||||
| chr6:136909527 | A | T | 1 | a0001c0001t0002g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-3931A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909527 | |||||||
| chr6:136909605 | A | G | 6 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0133 others(3): Show |
6 | HG02027.hp1 HG03490.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-3853A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909605 | |||||||
| chr6:136909633 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0074 |
2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.904-3825A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909633 | |||||||
| chr6:136909886 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.904-3572C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909886 | |||||||
| chr6:136909974 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.904-3484G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909974 | |||||||
| chr6:136909975 | G | A | 10 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.904-3483G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136909975 | |||||||
| chr6:136910021 | A | G | 10 | a0001c0001t0003g0007 a0001c0001t0003g0012 a0001c0001t0003g0013 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.904-3437A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910021 | |||||||
| chr6:136910136 | C | G | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0169 others(2): Show |
5 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-3322C>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910136 | |||||||
| chr6:136910156 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.904-3302T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910156 | |||||||
| chr6:136910211 | A | G | 8 | a0001c0001t0002g0017 a0001c0001t0002g0176 a0001c0001t0002g0266 others(5): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.904-3247A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910211 | |||||||
| chr6:136910269 | A | T | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.904-3189A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910269 | |||||||
| chr6:136910333 | A | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0128 others(9): Show |
13 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-3125A>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910333 | |||||||
| chr6:136910533 | A | G | 150 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0018 others(147): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-2925A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910533 | |||||||
| chr6:136910574 | A | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0102 a0001c0001t0001g0284 |
3 | HG01169.hp2 HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.904-2884A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910574 | |||||||
| chr6:136910584 | C | A | 1 | a0001c0001t0002g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-2874C>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910584 | |||||||
| chr6:136910785 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0001g0131 others(4): Show |
8 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.904-2673C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910785 | |||||||
| chr6:136910892 | C | T | 150 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0018 others(147): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-2566C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136910892 | |||||||
| chr6:136911041 | AT | A | 3 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0138 |
3 | NA18955.hp1 NA19062.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.904-2412delT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136911041 | ||||||
| chr6:136911417 | T | C | 9 | a0001c0001t0002g0017 a0001c0001t0002g0126 a0001c0001t0002g0176 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.904-2041T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911417 | |||||||
| chr6:136911459 | G | C | 1 | a0001c0001t0002g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-1999G>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911459 | |||||||
| chr6:136911596 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0074 |
2 | NA18956.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.904-1862G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911596 | |||||||
| chr6:136911636 | A | C | 15 | a0001c0001t0002g0062 a0001c0001t0002g0135 a0001c0001t0002g0137 others(12): Show |
15 | HG00544.hp1 HG02040.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.904-1822A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911636 | |||||||
| chr6:136911682 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.904-1776C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911682 | |||||||
| chr6:136911716 | A | AT | 150 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0018 others(147): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-1736dupT | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr6 | 136911716 | ||||||
| chr6:136911804 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.904-1654T>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911804 | |||||||
| chr6:136911860 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.904-1598C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136911860 | |||||||
| chr6:136912219 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.904-1239G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912219 | |||||||
| chr6:136912340 | G | A | 180 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0080 others(177): Show |
197 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.904-1118G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912340 | |||||||
| chr6:136912750 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0128 others(9): Show |
13 | HG00639.hp2 HG01192.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-708C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912750 | |||||||
| chr6:136912792 | A | G | 150 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0018 others(147): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-666A>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912792 | |||||||
| chr6:136912982 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.904-476C>T | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136912982 | |||||||
| chr6:136913025 | T | G | 150 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0018 others(147): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.904-433T>G | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913025 | |||||||
| chr6:136913135 | G | A | 2 | a0001c0001t0002g0257 a0001c0001t0002g0258 |
2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.904-323G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913135 | |||||||
| chr6:136913144 | A | C | 188 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0030 others(185): Show |
205 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.904-314A>C | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913144 | |||||||
| chr6:136913274 | G | A | 2 | a0001c0001t0009g0151 a0001c0001t0011g0148 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.904-184G>A | PEX7 | ENSG00000112357.14 | transcript | ENST00000318471.5 | protein_coding | 9/9 | chr6 | 136913274 |