Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5048 |
| ensemblid | ENSG00000007168.14 |
| hgncid | 8574 |
| symbol | PAFAH1B1 |
| name | platelet activating factor acetylhydrolase 1b regulatory subunit 1 |
| refseq_nuc | NM_000430.4 |
| refseq_prot | NP_000421.1 |
| ensembl_nuc | ENST00000397195.10 |
| ensembl_prot | ENSP00000380378.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 2593654 |
| end | 2685615 |
| strand | + |
| ver | v1.2 |
| region | chr17:2593654-2685615 |
| region5000 | chr17:2588654-2690615 |
| regionname0 | PAFAH1B1_chr17_2593654_2685615 |
| regionname5000 | PAFAH1B1_chr17_2588654_2690615 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1230 | 266 | 69 | 62 | 88 | 11 | 34 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | ATGGT others(1225): Show |
chr17 | 2588654 | 2690615 | ||
| a0001c0002 | 0/0 | 1230 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | ATGGT others(1225): Show |
chr17 | 2588654 | 2690615 | ||
| a0001c0003 | 0/0 | 1230 | 5 | 5 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | ATGGT others(1225): Show |
chr17 | 2588654 | 2690615 | ||
| a0001c0004 | 0/0 | 1230 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | ATGGT others(1225): Show |
chr17 | 2588654 | 2690615 | ||
| a0001c0005 | 0/0 | 1230 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | ATGGT others(1225): Show |
chr17 | 2588654 | 2690615 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5589 | 77 | 20 | 25 | 17 | 4 | 10 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0002 | 0/0 | 5587 | 48 | 1 | 7 | 29 | 4 | 7 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0003 | 1/0 | 5589 | 32 | 3 | 7 | 19 | 1 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0004 | 0/0 | 5589 | 26 | 9 | 9 | 1 | 1 | 6 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0005 | 0/0 | 5589 | 19 | 0 | 6 | 11 | 0 | 2 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0007 | 0/0 | 5589 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0008 | 0/0 | 5596 | 7 | 6 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5591): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0009 | 0/0 | 5589 | 6 | 0 | 0 | 5 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0010 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0011 | 0/0 | 5587 | 6 | 1 | 3 | 1 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0012 | 0/0 | 5596 | 5 | 4 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5591): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0013 | 0/0 | 5589 | 2 | 2 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0014 | 0/0 | 5589 | 2 | 0 | 0 | 0 | 0 | 2 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0015 | 0/0 | 5596 | 2 | 0 | 1 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5591): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0016 | 0/0 | 5589 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0017 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0018 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0019 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0020 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0021 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0022 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0023 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0024 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0025 | 0/0 | 5589 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0026 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0027 | 0/0 | 5587 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0028 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0029 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0030 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0031 | 0/0 | 5587 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0032 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0033 | 0/0 | 5589 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0034 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5599): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0035 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0037 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0038 | 0/0 | 5589 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0039 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5590): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0040 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5590): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0041 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5591): Show |
chr17 | 2588654 | 2690615 |
| a0001c0001t0042 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5591): Show |
chr17 | 2588654 | 2690615 |
| a0001c0002t0006 | 0/0 | 5587 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5582): Show |
chr17 | 2588654 | 2690615 |
| a0001c0003t0010 | 0/0 | 5589 | 5 | 5 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0004t0036 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| a0001c0005t0001 | 0/0 | 5589 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | AGACG others(5584): Show |
chr17 | 2588654 | 2690615 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0009g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0011g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0011g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0011g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0011g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0012g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0014g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0014g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0015g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0019g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0020g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0021g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0023g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0025g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0026g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0027g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0029g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0030g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0031g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0032g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0033g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0034g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0035g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0037g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0038g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0039g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0040g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0041g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0001t0042g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0003t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0003t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0003t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0003t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0003t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0004t0036g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | GBR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0090 | EUR | FIN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | FIN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00438 | hp2 | a0001 | c0001 | t0011 | g0270 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01109 | hp1 | a0001 | c0001 | t0015 | g0017 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0143 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01167 | hp2 | a0001 | c0001 | t0040 | g0074 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01243 | hp1 | a0001 | c0001 | t0039 | g0146 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01243 | hp2 | a0001 | c0001 | t0025 | g0031 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0276 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0101 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0167 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0098 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01993 | hp2 | a0001 | c0001 | t0011 | g0242 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02004 | hp2 | a0001 | c0001 | t0011 | g0239 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02055 | hp1 | a0001 | c0002 | t0006 | g0190 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0196 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02165 | hp1 | a0001 | c0001 | t0034 | g0251 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0086 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0144 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02258 | hp1 | a0001 | c0001 | t0022 | g0183 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0100 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02273 | hp2 | a0001 | c0001 | t0011 | g0241 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0191 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0097 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0137 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02572 | hp2 | a0001 | c0001 | t0030 | g0106 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02602 | hp2 | a0001 | c0001 | t0038 | g0238 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0181 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0189 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02647 | hp2 | a0001 | c0003 | t0010 | g0179 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0211 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02698 | hp1 | a0001 | c0001 | t0011 | g0233 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02723 | hp1 | a0001 | c0001 | t0035 | g0204 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02738 | hp2 | a0001 | c0001 | t0027 | g0159 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02809 | hp1 | a0001 | c0002 | t0006 | g0188 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0022 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02886 | hp2 | a0001 | c0003 | t0010 | g0178 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02896 | hp1 | a0001 | c0003 | t0010 | g0177 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0012 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02976 | hp1 | a0001 | c0003 | t0010 | g0175 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03017 | hp2 | a0001 | c0001 | t0014 | g0048 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0186 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0185 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03139 | hp1 | a0001 | c0001 | t0032 | g0197 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03195 | hp1 | a0001 | c0003 | t0010 | g0176 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03209 | hp1 | a0001 | c0001 | t0026 | g0088 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03209 | hp2 | a0001 | c0001 | t0029 | g0182 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03225 | hp2 | a0001 | c0001 | t0042 | g0015 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0218 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03453 | hp2 | a0001 | c0001 | t0037 | g0272 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0247 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0016 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0274 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03579 | hp2 | a0001 | c0001 | t0023 | g0135 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03704 | hp2 | a0001 | c0001 | t0031 | g0087 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0092 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04199 | hp2 | a0001 | c0001 | t0015 | g0280 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04204 | hp1 | a0001 | c0001 | t0012 | g0279 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG04228 | hp2 | a0001 | c0001 | t0014 | g0047 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | YRI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | YRI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0082 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18946 | hp2 | a0001 | c0001 | t0033 | g0026 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18948 | hp2 | a0001 | c0001 | t0009 | g0061 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18968 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18979 | hp2 | a0001 | c0001 | t0020 | g0226 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18983 | hp1 | a0001 | c0001 | t0019 | g0268 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19030 | hp1 | a0001 | c0004 | t0036 | g0205 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0193 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0107 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19063 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0140 | AFR | ASW | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | ASW | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0237 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0208 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0093 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0081 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02109 | hp2 | a0001 | c0002 | t0006 | g0187 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0253 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG03471 | hp2 | a0001 | c0001 | t0021 | g0180 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG06807 | hp1 | a0001 | c0001 | t0028 | g0018 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0142 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20300 | hp1 | a0001 | c0001 | t0041 | g0139 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0240 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| NA21309 | hp2 | a0001 | c0001 | t0017 | g0010 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0173 | REF | REF | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0103 | REF | REF | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:2670237 | C | T | 1 | a0001c0003 | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.474C>T | p.Phe158Phe | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/11 | 1017/5589 | 474/1233 | 158/410 | chr17 | 2670237 | |||
| chr17:2674081 | A | T | 1 | a0001c0002 | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
synonymous_variant | LOW | c.693A>T | p.Thr231Thr | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/11 | 1236/5589 | 693/1233 | 231/410 | chr17 | 2674081 | |||
| chr17:2674168 | A | G | 1 | a0001c0005 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.780A>G | p.Val260Val | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/11 | 1323/5589 | 780/1233 | 260/410 | chr17 | 2674168 | |||
| chr17:2680220 | T | C | 1 | a0001c0004 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1059T>C | p.Ile353Ile | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/11 | 1602/5589 | 1059/1233 | 353/410 | chr17 | 2680220 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:2593657 | C | CGGAGCT | 7 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(4): Show |
18 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-534_-529dupTGGAGC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44620 | INFO_REALIGN_3_PRIME | chr17 | 2593657 | |||||
| chr17:2593717 | G | T | 1 | a0001c0001t0038 | 1 | HG02602.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-480G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | chr17 | 2593717 | |||||||
| chr17:2593891 | C | A | 1 | a0001c0001t0013 | 2 | HG03453.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-306C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44398 | chr17 | 2593891 | ||||||
| chr17:2593898 | C | T | 3 | a0001c0001t0007 a0001c0001t0037 a0001c0004t0036 |
9 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-299C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44391 | chr17 | 2593898 | ||||||
| chr17:2593902 | C | CCCTCCCT others(8): Show |
1 | a0001c0001t0034 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-284_-270dupTCCTTC others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44361 | INFO_REALIGN_3_PRIME | chr17 | 2593902 | |||||
| chr17:2593927 | C | T | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-270C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44362 | chr17 | 2593927 | ||||||
| chr17:2638186 | T | C | 1 | a0001c0001t0014 | 2 | HG03017.hp2 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-103T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/11 | 103 | chr17 | 2638186 | ||||||
| chr17:2638205 | A | T | 1 | a0001c0001t0038 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/11 | 84 | chr17 | 2638205 | ||||||
| chr17:2638240 | A | C | 1 | a0001c0001t0033 | 1 | NA18946.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/11 | 49 | chr17 | 2638240 | ||||||
| chr17:2681819 | C | T | 6 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0032 others(3): Show |
36 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*17C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 17 | chr17 | 2681819 | ||||||
| chr17:2681866 | A | AC | 5 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(2): Show |
16 | HG01109.hp1 HG01167.hp1 HG01884.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*68dupC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 69 | INFO_REALIGN_3_PRIME | chr17 | 2681866 | |||||
| chr17:2682488 | T | A | 2 | a0001c0001t0009 a0001c0001t0016 |
7 | HG00323.hp1 NA18944.hp1 NA18948.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*686T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 686 | chr17 | 2682488 | ||||||
| chr17:2682503 | C | T | 1 | a0001c0002t0006 | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*701C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 701 | chr17 | 2682503 | ||||||
| chr17:2682855 | G | A | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0004t0036 |
3 | HG02809.hp2 NA19030.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1053G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1053 | chr17 | 2682855 | ||||||
| chr17:2682935 | A | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(23): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*1133A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1133 | chr17 | 2682935 | ||||||
| chr17:2682955 | C | T | 1 | a0001c0001t0023 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1153 | chr17 | 2682955 | ||||||
| chr17:2683180 | G | A | 2 | a0001c0001t0024 a0001c0002t0006 |
8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1378G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1378 | chr17 | 2683180 | ||||||
| chr17:2683264 | C | G | 1 | a0001c0001t0022 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1462 | chr17 | 2683264 | ||||||
| chr17:2683716 | A | T | 3 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0033 |
21 | HG00597.hp2 HG00609.hp1 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1914A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1914 | chr17 | 2683716 | ||||||
| chr17:2683733 | GAA | G | 1 | a0001c0002t0006 | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1934_*1935delAA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 2683733 | |||||
| chr17:2683793 | T | C | 5 | a0001c0001t0008 a0001c0001t0025 a0001c0001t0026 others(2): Show |
11 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1991T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1991 | chr17 | 2683793 | ||||||
| chr17:2683942 | A | G | 5 | a0001c0001t0012 a0001c0001t0018 a0001c0001t0022 others(2): Show |
9 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2140A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 2140 | chr17 | 2683942 | ||||||
| chr17:2683988 | C | T | 1 | a0001c0001t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2186C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 2186 | chr17 | 2683988 | ||||||
| chr17:2684594 | T | C | 1 | a0001c0001t0027 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2792T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 2792 | chr17 | 2684594 | ||||||
| chr17:2684865 | G | A | 1 | a0001c0001t0019 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3063 | chr17 | 2684865 | ||||||
| chr17:2684989 | C | T | 11 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0021 others(8): Show |
15 | HG02630.hp2 HG02647.hp2 HG02886.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3187C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3187 | chr17 | 2684989 | ||||||
| chr17:2685165 | A | G | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3363A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3363 | chr17 | 2685165 | ||||||
| chr17:2685428 | TAA | T | 7 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0019 others(4): Show |
59 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3627_*3628delAA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3627 | chr17 | 2685428 | ||||||
| chr17:2685473 | A | G | 1 | a0001c0001t0016 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3671A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3671 | chr17 | 2685473 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:2594030 | C | T | 2 | a0001c0001t0012g0279 a0001c0001t0015g0280 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-191+24C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594030 | |||||||
| chr17:2594149 | T | G | 1 | a0001c0001t0016g0001 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-191+143T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594149 | |||||||
| chr17:2594424 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-191+418G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594424 | |||||||
| chr17:2594755 | A | G | 84 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 others(81): Show |
84 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-191+749A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594755 | |||||||
| chr17:2594816 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-191+810G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594816 | |||||||
| chr17:2594912 | G | A | 1 | a0001c0001t0007g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-191+906G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594912 | |||||||
| chr17:2595054 | G | A | 1 | a0001c0001t0005g0004 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-191+1048G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595054 | |||||||
| chr17:2595162 | TCTTTC | T | 8 | a0001c0001t0004g0198 a0001c0001t0004g0199 a0001c0001t0004g0200 others(5): Show |
8 | HG01070.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+1160_-191+116 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595162 | ||||||
| chr17:2595260 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-191+1254C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595260 | |||||||
| chr17:2595340 | G | T | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-191+1334G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595340 | |||||||
| chr17:2595421 | C | CTTTTT | 62 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0217 others(59): Show |
62 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-191+1427_-191+143 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595421 | ||||||
| chr17:2595421 | C | CTTTTTT | 11 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0004g0275 others(8): Show |
11 | HG00438.hp2 HG01257.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-191+1426_-191+143 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595421 | ||||||
| chr17:2595421 | CT | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(13): Show |
16 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-191+1431delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595421 | ||||||
| chr17:2595435 | T | TTTTTC | 17 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-191+1431_-191+143 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595435 | ||||||
| chr17:2595477 | CAT | C | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+1473_-191+147 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595477 | ||||||
| chr17:2595566 | A | G | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+1560A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595566 | |||||||
| chr17:2595599 | G | T | 20 | a0001c0001t0003g0002 a0001c0001t0003g0216 a0001c0001t0003g0254 others(17): Show |
20 | HG01346.hp1 HG01496.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-191+1593G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595599 | |||||||
| chr17:2596184 | G | A | 1 | a0001c0001t0012g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-191+2178G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596184 | |||||||
| chr17:2596196 | A | G | 9 | a0001c0001t0003g0011 a0001c0001t0012g0012 a0001c0001t0012g0013 others(6): Show |
9 | HG01109.hp1 HG01515.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-191+2190A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596196 | |||||||
| chr17:2596253 | C | T | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+2247C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596253 | |||||||
| chr17:2596293 | G | T | 1 | a0001c0001t0013g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-191+2287G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596293 | |||||||
| chr17:2596608 | C | T | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191+2602C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596608 | |||||||
| chr17:2596652 | A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+2646A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596652 | |||||||
| chr17:2596780 | C | G | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191+2774C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596780 | |||||||
| chr17:2596986 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0028g0018 |
3 | HG02559.hp2 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-191+2980G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596986 | |||||||
| chr17:2597011 | A | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+3005A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597011 | |||||||
| chr17:2597024 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-191+3018G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597024 | |||||||
| chr17:2597149 | G | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+3143G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597149 | |||||||
| chr17:2597399 | G | T | 74 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(71): Show |
74 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.-191+3393G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597399 | |||||||
| chr17:2597403 | C | CT | 51 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0161 others(48): Show |
51 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-191+3422dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | ||||||
| chr17:2597403 | C | CTT | 15 | a0001c0001t0001g0021 a0001c0001t0001g0174 a0001c0001t0003g0216 others(12): Show |
15 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.-191+3421_-191+342 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | ||||||
| chr17:2597403 | C | CTTT | 35 | a0001c0001t0002g0234 a0001c0001t0004g0198 a0001c0001t0004g0199 others(32): Show |
35 | HG00733.hp1 HG01070.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.-191+3420_-191+342 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | ||||||
| chr17:2597403 | CT | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(27): Show |
30 | HG01070.hp2 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-191+3422delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | ||||||
| chr17:2597403 | CTT | C | 6 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-191+3421_-191+342 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | ||||||
| chr17:2597652 | G | C | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+3646G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597652 | |||||||
| chr17:2597679 | A | G | 78 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(75): Show |
78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+3673A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597679 | |||||||
| chr17:2597742 | TTCTC | T | 77 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(74): Show |
77 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.-191+3741_-191+374 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597742 | ||||||
| chr17:2597781 | A | AGT | 79 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(76): Show |
79 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.-191+3792_-191+379 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597781 | ||||||
| chr17:2598105 | C | T | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+4099C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598105 | |||||||
| chr17:2598152 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
4 | HG01243.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-191+4146G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598152 | |||||||
| chr17:2598256 | T | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0153 |
2 | HG00642.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-191+4250T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598256 | |||||||
| chr17:2598474 | C | T | 5 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 others(2): Show |
5 | HG00558.hp1 NA18612.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+4468C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598474 | |||||||
| chr17:2599092 | T | C | 78 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(75): Show |
78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+5086T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599092 | |||||||
| chr17:2599347 | C | T | 1 | a0001c0001t0004g0252 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-191+5341C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599347 | |||||||
| chr17:2599402 | T | G | 2 | a0001c0001t0004g0228 a0001c0001t0004g0252 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-191+5396T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599402 | |||||||
| chr17:2599656 | A | G | 1 | a0001c0001t0015g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-191+5650A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599656 | |||||||
| chr17:2599712 | A | G | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+5706A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599712 | |||||||
| chr17:2599767 | C | T | 1 | a0001c0001t0007g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-191+5761C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599767 | |||||||
| chr17:2599876 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-191+5870A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599876 | |||||||
| chr17:2599971 | C | CT | 49 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(46): Show |
49 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.-191+5990dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | ||||||
| chr17:2599971 | C | CTT | 5 | a0001c0001t0001g0145 a0001c0001t0012g0016 a0001c0001t0022g0183 others(2): Show |
5 | HG01243.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+5989_-191+599 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | ||||||
| chr17:2599971 | CT | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
76 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.-191+5990delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | ||||||
| chr17:2599971 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+5978_-191+599 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | ||||||
| chr17:2600103 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-191+6097C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600103 | |||||||
| chr17:2600104 | C | T | 18 | a0001c0001t0002g0122 a0001c0001t0008g0137 a0001c0001t0008g0138 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-191+6098C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600104 | |||||||
| chr17:2600154 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-191+6148A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600154 | |||||||
| chr17:2600250 | C | A | 19 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(16): Show |
19 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-191+6244C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600250 | |||||||
| chr17:2600283 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-191+6277T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600283 | |||||||
| chr17:2600568 | C | CA | 98 | a0001c0001t0001g0039 a0001c0001t0001g0123 a0001c0001t0001g0154 others(95): Show |
98 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.-191+6580dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2600568 | ||||||
| chr17:2600568 | C | CAA | 7 | a0001c0001t0003g0216 a0001c0001t0003g0217 a0001c0001t0003g0254 others(4): Show |
7 | HG01261.hp2 HG01952.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+6579_-191+658 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2600568 | ||||||
| chr17:2600587 | C | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+6581C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600587 | |||||||
| chr17:2600769 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+6763G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600769 | |||||||
| chr17:2600819 | T | C | 77 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(74): Show |
77 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.-191+6813T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600819 | |||||||
| chr17:2600864 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+6858C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600864 | |||||||
| chr17:2600932 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-191+6926A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600932 | |||||||
| chr17:2600952 | G | A | 1 | a0001c0001t0025g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-191+6946G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600952 | |||||||
| chr17:2600974 | T | C | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0016 |
3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-191+6968T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600974 | |||||||
| chr17:2601254 | C | T | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-191+7248C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601254 | |||||||
| chr17:2601409 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-191+7403A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601409 | |||||||
| chr17:2601508 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+7502C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601508 | |||||||
| chr17:2601511 | G | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+7505G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601511 | |||||||
| chr17:2601566 | C | T | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+7560C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601566 | |||||||
| chr17:2601584 | G | GGT | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+7580_-191+758 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2601584 | ||||||
| chr17:2601593 | C | T | 1 | a0001c0001t0005g0004 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-191+7587C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601593 | |||||||
| chr17:2601693 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-191+7687C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601693 | |||||||
| chr17:2601993 | A | G | 76 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(73): Show |
76 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-191+7987A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601993 | |||||||
| chr17:2602089 | TACCATGA others(7): Show |
T | 3 | a0001c0001t0001g0039 a0001c0001t0002g0118 a0001c0001t0002g0119 |
3 | HG00544.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-191+8084_-191+809 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602089 | |||||||
| chr17:2602251 | G | GA | 32 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(29): Show |
32 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-191+8255dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2602251 | ||||||
| chr17:2602264 | A | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+8258A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602264 | |||||||
| chr17:2602539 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-191+8533C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602539 | |||||||
| chr17:2602807 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(14): Show |
17 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-191+8801G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602807 | |||||||
| chr17:2602908 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-191+8902G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602908 | |||||||
| chr17:2603335 | T | C | 3 | a0001c0001t0002g0037 a0001c0001t0002g0056 a0001c0001t0002g0156 |
3 | NA18944.hp2 NA18952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-191+9329T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603335 | |||||||
| chr17:2603538 | T | C | 73 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(70): Show |
73 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.-191+9532T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603538 | |||||||
| chr17:2603741 | C | CT | 29 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0229 others(26): Show |
29 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.-191+9749dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2603741 | ||||||
| chr17:2603741 | CT | C | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+9749delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2603741 | ||||||
| chr17:2603836 | G | A | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+9830G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603836 | |||||||
| chr17:2603894 | C | T | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-191+9888C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603894 | |||||||
| chr17:2603971 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-191+9965C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603971 | |||||||
| chr17:2604015 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0002g0115 |
3 | HG00544.hp2 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-191+10009C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604015 | |||||||
| chr17:2604067 | G | C | 1 | a0001c0001t0005g0058 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-191+10061G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604067 | |||||||
| chr17:2604127 | T | C | 12 | a0001c0001t0003g0216 a0001c0001t0003g0254 a0001c0001t0003g0255 others(9): Show |
12 | NA18947.hp1 NA18952.hp2 NA18965.hp1 others(9): Show |
intron_variant | MODIFIER | c.-191+10121T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604127 | |||||||
| chr17:2604198 | C | T | 2 | a0001c0001t0004g0228 a0001c0001t0004g0252 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-191+10192C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604198 | |||||||
| chr17:2604203 | A | G | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+10197A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604203 | |||||||
| chr17:2604291 | G | C | 7 | a0001c0001t0003g0002 a0001c0001t0003g0264 a0001c0001t0003g0265 others(4): Show |
7 | HG01346.hp1 HG01496.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+10285G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604291 | |||||||
| chr17:2604318 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191+10312G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604318 | |||||||
| chr17:2604493 | T | C | 2 | a0001c0001t0004g0228 a0001c0001t0004g0252 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-191+10487T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604493 | |||||||
| chr17:2604689 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-191+10683T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604689 | |||||||
| chr17:2604809 | C | CA | 9 | a0001c0001t0004g0198 a0001c0002t0006g0185 a0001c0002t0006g0186 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-191+10813dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2604809 | ||||||
| chr17:2604955 | G | A | 96 | a0001c0001t0001g0184 a0001c0001t0001g0220 a0001c0001t0002g0234 others(93): Show |
96 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.-191+10949G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604955 | |||||||
| chr17:2605002 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-191+10996G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605002 | |||||||
| chr17:2605056 | T | C | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+11050T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605056 | |||||||
| chr17:2605085 | C | T | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+11079C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605085 | |||||||
| chr17:2605258 | T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+11252T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605258 | |||||||
| chr17:2605617 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-191+11611G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605617 | |||||||
| chr17:2605619 | G | A | 1 | a0001c0001t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-191+11613G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605619 | |||||||
| chr17:2605689 | C | G | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+11683C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605689 | |||||||
| chr17:2605762 | G | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-191+11756G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605762 | |||||||
| chr17:2605785 | G | T | 9 | a0001c0001t0001g0109 a0001c0001t0002g0038 a0001c0001t0002g0108 others(6): Show |
9 | HG00438.hp1 HG00558.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-191+11779G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605785 | |||||||
| chr17:2605855 | A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+11849A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605855 | |||||||
| chr17:2605866 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-191+11860G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605866 | |||||||
| chr17:2605871 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-191+11865T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605871 | |||||||
| chr17:2605903 | G | T | 3 | a0001c0001t0003g0217 a0001c0001t0013g0218 a0001c0001t0013g0253 |
3 | HG03453.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-191+11897G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605903 | |||||||
| chr17:2606002 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-191+11996A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606002 | |||||||
| chr17:2606067 | C | T | 74 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(71): Show |
74 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.-191+12061C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606067 | |||||||
| chr17:2606426 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-191+12420C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606426 | |||||||
| chr17:2606525 | G | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-191+12519G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606525 | |||||||
| chr17:2606732 | G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+12726G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606732 | |||||||
| chr17:2606803 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-191+12797C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606803 | |||||||
| chr17:2606810 | C | CT | 21 | a0001c0001t0001g0132 a0001c0001t0001g0145 a0001c0001t0001g0174 others(18): Show |
21 | HG00438.hp1 HG00438.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-191+12831dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | ||||||
| chr17:2606810 | CT | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0027 others(26): Show |
29 | HG00733.hp2 HG01243.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.-191+12831delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | ||||||
| chr17:2606810 | CTT | C | 9 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(6): Show |
9 | HG01891.hp1 HG02647.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-191+12830_-191+12 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | ||||||
| chr17:2606810 | CTTTT | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+12828_-191+12 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | ||||||
| chr17:2606859 | G | A | 78 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(75): Show |
78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+12853G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606859 | |||||||
| chr17:2606885 | C | T | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-191+12879C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606885 | |||||||
| chr17:2607018 | G | A | 77 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(74): Show |
77 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.-191+13012G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607018 | |||||||
| chr17:2607085 | C | T | 78 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(75): Show |
78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+13079C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607085 | |||||||
| chr17:2607244 | G | A | 3 | a0001c0001t0004g0275 a0001c0001t0013g0218 a0001c0001t0013g0253 |
3 | HG02486.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+13238G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607244 | |||||||
| chr17:2607497 | T | C | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0016 |
3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-191+13491T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607497 | |||||||
| chr17:2607518 | T | C | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-191+13512T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607518 | |||||||
| chr17:2607558 | C | G | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-191+13552C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607558 | |||||||
| chr17:2607567 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-191+13561C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607567 | |||||||
| chr17:2608099 | T | G | 1 | a0001c0001t0020g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-191+14093T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608099 | |||||||
| chr17:2608281 | G | T | 3 | a0001c0001t0003g0217 a0001c0001t0013g0218 a0001c0001t0013g0253 |
3 | HG03453.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-191+14275G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608281 | |||||||
| chr17:2608316 | C | T | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-191+14310C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608316 | |||||||
| chr17:2608402 | T | C | 18 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-191+14396T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608402 | |||||||
| chr17:2608545 | G | A | 1 | a0001c0001t0022g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-191+14539G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608545 | |||||||
| chr17:2608624 | A | T | 1 | a0001c0001t0030g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-191+14618A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608624 | |||||||
| chr17:2608782 | G | C | 1 | a0001c0001t0002g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-191+14776G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608782 | |||||||
| chr17:2608826 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+14820A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608826 | |||||||
| chr17:2609191 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+15185C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609191 | |||||||
| chr17:2609530 | T | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-191+15524T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609530 | |||||||
| chr17:2609581 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-191+15575C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609581 | |||||||
| chr17:2609621 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+15615C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609621 | |||||||
| chr17:2609656 | C | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+15650C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609656 | |||||||
| chr17:2609689 | T | G | 1 | a0001c0001t0003g0278 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-191+15683T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609689 | |||||||
| chr17:2609756 | C | T | 18 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-191+15750C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609756 | |||||||
| chr17:2610394 | A | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-191+16388A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2610394 | |||||||
| chr17:2610691 | T | C | 1 | a0001c0001t0042g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-191+16685T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2610691 | |||||||
| chr17:2610857 | C | T | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0122 others(1): Show |
4 | HG02015.hp1 NA18612.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191+16851C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2610857 | |||||||
| chr17:2611265 | C | T | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191+17259C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611265 | |||||||
| chr17:2611479 | A | AT | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+17473_-191+17 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611479 | |||||||
| chr17:2611479 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-191+17473A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611479 | |||||||
| chr17:2611693 | C | T | 1 | a0001c0001t0004g0248 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-191+17687C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611693 | |||||||
| chr17:2611694 | G | A | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-191+17688G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611694 | |||||||
| chr17:2611707 | C | G | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-191+17701C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611707 | |||||||
| chr17:2612210 | C | CT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0105 others(10): Show |
13 | HG01261.hp1 HG01433.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.-191+18220dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2612210 | ||||||
| chr17:2612303 | G | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
268 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.-191+18297G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612303 | |||||||
| chr17:2612344 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-191+18338C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612344 | |||||||
| chr17:2612351 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0002g0133 a0001c0001t0002g0136 |
3 | HG02735.hp1 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-191+18345G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612351 | |||||||
| chr17:2612522 | A | G | 8 | a0001c0001t0003g0099 a0001c0001t0005g0097 a0001c0001t0005g0098 others(5): Show |
8 | HG00558.hp2 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.-191+18516A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612522 | |||||||
| chr17:2612588 | C | T | 2 | a0001c0001t0012g0279 a0001c0001t0015g0280 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-191+18582C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612588 | |||||||
| chr17:2612732 | C | A | 1 | a0001c0001t0003g0224 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-191+18726C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612732 | |||||||
| chr17:2612775 | T | C | 2 | a0001c0001t0010g0181 a0001c0001t0021g0180 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-191+18769T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612775 | |||||||
| chr17:2612908 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-191+18902C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612908 | |||||||
| chr17:2612975 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-191+18969C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612975 | |||||||
| chr17:2613004 | A | G | 1 | a0001c0001t0003g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-191+18998A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613004 | |||||||
| chr17:2613042 | T | TA | 6 | a0001c0001t0001g0041 a0001c0001t0001g0145 a0001c0001t0001g0154 others(3): Show |
6 | HG01433.hp2 HG02572.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.-191+19054dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | ||||||
| chr17:2613042 | TA | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(30): Show |
33 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-191+19054delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | ||||||
| chr17:2613042 | TAA | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-191+19053_-191+19 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | ||||||
| chr17:2613042 | TAAA | T | 72 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(69): Show |
72 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.-191+19052_-191+19 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | ||||||
| chr17:2613115 | TTTTC | T | 72 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(69): Show |
72 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.-191+19117_-191+19 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613115 | ||||||
| chr17:2613435 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(1): Show |
4 | HG02258.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191+19429T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613435 | |||||||
| chr17:2613474 | C | A | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-191+19468C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613474 | |||||||
| chr17:2613518 | G | T | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-191+19512G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613518 | |||||||
| chr17:2613640 | T | C | 97 | a0001c0001t0001g0184 a0001c0001t0001g0220 a0001c0001t0002g0234 others(94): Show |
97 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.-191+19634T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613640 | |||||||
| chr17:2613667 | C | T | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-191+19661C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613667 | |||||||
| chr17:2613697 | A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+19691A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613697 | |||||||
| chr17:2613737 | C | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG00099.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-191+19731C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613737 | |||||||
| chr17:2613828 | G | T | 78 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(75): Show |
78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+19822G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613828 | |||||||
| chr17:2613839 | C | T | 2 | a0001c0001t0008g0143 a0001c0001t0008g0144 |
2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-191+19833C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613839 | |||||||
| chr17:2613855 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-191+19849G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613855 | |||||||
| chr17:2613928 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+19922G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613928 | |||||||
| chr17:2614021 | G | GT | 93 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(90): Show |
93 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-191+20036dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | ||||||
| chr17:2614021 | G | GTT | 27 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0036 others(24): Show |
27 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.-191+20035_-191+20 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | ||||||
| chr17:2614021 | G | GTTT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0003g0011 others(18): Show |
21 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.-191+20034_-191+20 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | ||||||
| chr17:2614021 | G | GTTTT | 15 | a0001c0001t0001g0008 a0001c0001t0003g0224 a0001c0001t0008g0141 others(12): Show |
15 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-191+20033_-191+20 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | ||||||
| chr17:2614021 | G | GTTTTT | 52 | a0001c0001t0001g0184 a0001c0001t0001g0220 a0001c0001t0002g0234 others(49): Show |
52 | HG00733.hp1 HG00738.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.-191+20032_-191+20 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | ||||||
| chr17:2614021 | G | GTTTTTT | 20 | a0001c0001t0003g0216 a0001c0001t0003g0223 a0001c0001t0003g0254 others(17): Show |
20 | HG00438.hp2 HG01496.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-191+20031_-191+20 others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | ||||||
| chr17:2614207 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02258.hp2 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-191+20201G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614207 | |||||||
| chr17:2614263 | A | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+20257A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614263 | |||||||
| chr17:2614414 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-191+20408A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614414 | |||||||
| chr17:2614483 | A | T | 1 | a0001c0001t0004g0246 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-191+20477A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614483 | |||||||
| chr17:2614786 | C | G | 24 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0044 others(21): Show |
24 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-191+20780C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614786 | |||||||
| chr17:2614804 | T | C | 13 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
13 | HG00735.hp2 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-191+20798T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614804 | |||||||
| chr17:2614811 | C | T | 1 | a0001c0001t0008g0144 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-191+20805C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614811 | |||||||
| chr17:2615011 | T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+21005T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615011 | |||||||
| chr17:2615038 | C | CTCCA | 78 | a0001c0001t0001g0220 a0001c0001t0002g0234 a0001c0001t0003g0002 others(75): Show |
78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+21033_-191+21 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2615038 | ||||||
| chr17:2615086 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-191+21080A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615086 | |||||||
| chr17:2615271 | C | G | 1 | a0001c0001t0002g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-191+21265C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615271 | |||||||
| chr17:2615365 | A | G | 71 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0216 others(68): Show |
71 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.-191+21359A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615365 | |||||||
| chr17:2615432 | A | G | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.-191+21426A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615432 | |||||||
| chr17:2615480 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-191+21474G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615480 | |||||||
| chr17:2615555 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(14): Show |
17 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-191+21549C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615555 | |||||||
| chr17:2615578 | C | T | 92 | a0001c0001t0001g0184 a0001c0001t0002g0234 a0001c0001t0003g0002 others(89): Show |
92 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.-191+21572C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615578 | |||||||
| chr17:2615852 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-191+21846G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615852 | |||||||
| chr17:2616011 | G | T | 1 | a0001c0001t0008g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-191+22005G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616011 | |||||||
| chr17:2616027 | C | G | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-191+22021C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616027 | |||||||
| chr17:2616060 | A | G | 1 | a0001c0001t0008g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-190-22039A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616060 | |||||||
| chr17:2616313 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-190-21786C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616313 | |||||||
| chr17:2616335 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-190-21764G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616335 | |||||||
| chr17:2616337 | G | A | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-21762G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616337 | |||||||
| chr17:2616440 | C | T | 27 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0229 others(24): Show |
27 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-190-21659C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616440 | |||||||
| chr17:2616504 | A | G | 1 | a0001c0001t0009g0061 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-190-21595A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616504 | |||||||
| chr17:2616672 | C | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-21427C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616672 | |||||||
| chr17:2616834 | C | T | 13 | a0001c0001t0023g0135 a0001c0002t0006g0185 a0001c0002t0006g0186 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190-21265C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616834 | |||||||
| chr17:2617063 | A | C | 2 | a0001c0001t0004g0228 a0001c0001t0004g0252 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-190-21036A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617063 | |||||||
| chr17:2617321 | C | T | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-20778C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617321 | |||||||
| chr17:2617342 | C | A | 4 | a0001c0001t0003g0217 a0001c0001t0013g0218 a0001c0001t0013g0253 others(1): Show |
4 | HG03453.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-20757C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617342 | |||||||
| chr17:2617412 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-20687T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617412 | |||||||
| chr17:2617645 | TGGTGGCT others(324): Show |
T | 1 | a0001c0003t0010g0175 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-190-20416_-190-20 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2617645 | ||||||
| chr17:2617977 | G | A | 4 | a0001c0001t0003g0217 a0001c0001t0013g0218 a0001c0001t0013g0253 others(1): Show |
4 | HG03453.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-20122G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617977 | |||||||
| chr17:2618063 | A | T | 1 | a0001c0005t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-190-20036A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618063 | |||||||
| chr17:2618228 | G | A | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-19871G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618228 | |||||||
| chr17:2618489 | A | G | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0016 |
3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-190-19610A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618489 | |||||||
| chr17:2618631 | T | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-19468T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618631 | |||||||
| chr17:2618837 | G | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
113 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(110): Show |
intron_variant | MODIFIER | c.-190-19262G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618837 | |||||||
| chr17:2618954 | C | CA | 44 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0039 others(41): Show |
44 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.-190-19122dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | ||||||
| chr17:2618954 | C | CAA | 13 | a0001c0001t0001g0164 a0001c0001t0002g0037 a0001c0001t0002g0056 others(10): Show |
13 | HG00558.hp1 HG00597.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-190-19123_-190-19 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | ||||||
| chr17:2618954 | CA | C | 91 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
91 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190-19122delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | ||||||
| chr17:2618954 | CAA | C | 7 | a0001c0001t0003g0217 a0001c0001t0004g0198 a0001c0001t0004g0202 others(4): Show |
7 | HG01070.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-19123_-190-19 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | ||||||
| chr17:2618954 | CAAA | C | 11 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-190-19124_-190-19 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | ||||||
| chr17:2618995 | A | G | 1 | a0001c0001t0003g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-190-19104A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618995 | |||||||
| chr17:2619199 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-18900T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619199 | |||||||
| chr17:2619273 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-190-18826C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619273 | |||||||
| chr17:2619364 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-190-18735G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619364 | |||||||
| chr17:2619382 | C | T | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-18717C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619382 | |||||||
| chr17:2619405 | A | T | 6 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 others(3): Show |
6 | HG01071.hp1 HG01074.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190-18694A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619405 | |||||||
| chr17:2619406 | T | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-18693T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619406 | |||||||
| chr17:2619534 | C | CTGTTTTT others(3): Show |
93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
93 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.-190-18563_-190-18 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619534 | ||||||
| chr17:2619534 | C | CTGTTTTT others(4): Show |
17 | a0001c0001t0001g0184 a0001c0001t0003g0225 a0001c0001t0003g0227 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190-18554_-190-18 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619534 | ||||||
| chr17:2619534 | CTGTTTTT others(4): Show |
C | 25 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(22): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-190-18554_-190-18 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619534 | ||||||
| chr17:2619536 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0015g0017 a0001c0001t0032g0197 |
2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-190-18554_-190-18 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619536 | ||||||
| chr17:2619536 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-18562_-190-18 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619536 | ||||||
| chr17:2620052 | G | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-18047G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620052 | |||||||
| chr17:2620584 | C | T | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-17515C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620584 | |||||||
| chr17:2620595 | T | A | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-190-17504T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620595 | |||||||
| chr17:2620626 | G | T | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-17473G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620626 | |||||||
| chr17:2620697 | A | G | 1 | a0001c0001t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-190-17402A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620697 | |||||||
| chr17:2620908 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-190-17191A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620908 | |||||||
| chr17:2620972 | TC | T | 19 | a0001c0001t0001g0184 a0001c0001t0003g0217 a0001c0001t0013g0218 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-190-17125delC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2620972 | ||||||
| chr17:2621038 | G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-17061G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621038 | |||||||
| chr17:2621049 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-17050T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621049 | |||||||
| chr17:2621082 | TTC | T | 4 | a0001c0001t0003g0002 a0001c0001t0003g0264 a0001c0001t0003g0265 others(1): Show |
4 | HG01346.hp1 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-17015_-190-17 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621082 | ||||||
| chr17:2621227 | T | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
119 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-16872T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621227 | |||||||
| chr17:2621572 | T | TA | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-16525dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621572 | ||||||
| chr17:2621605 | GTCTTTT | G | 7 | a0001c0001t0001g0184 a0001c0001t0007g0196 a0001c0001t0007g0213 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT | G | 12 | a0001c0001t0003g0219 a0001c0001t0003g0223 a0001c0001t0003g0261 others(9): Show |
12 | HG00735.hp1 HG01978.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(13): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(1): Show |
G | 32 | a0001c0001t0003g0002 a0001c0001t0003g0216 a0001c0001t0003g0221 others(29): Show |
32 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(2): Show |
G | 21 | a0001c0001t0002g0234 a0001c0001t0003g0217 a0001c0001t0004g0202 others(18): Show |
21 | HG01168.hp2 HG01255.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(15): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(3): Show |
G | 2 | a0001c0001t0004g0198 a0001c0001t0004g0276 |
2 | HG01257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(4): Show |
G | 7 | a0001c0001t0018g0022 a0001c0001t0023g0135 a0001c0003t0010g0175 others(4): Show |
7 | HG02647.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(5): Show |
G | 2 | a0001c0001t0012g0014 a0001c0001t0015g0017 |
2 | HG01109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(6): Show |
G | 15 | a0001c0001t0008g0138 a0001c0001t0008g0140 a0001c0001t0008g0141 others(12): Show |
15 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(19): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(7): Show |
G | 6 | a0001c0001t0003g0011 a0001c0001t0003g0225 a0001c0001t0003g0227 others(3): Show |
6 | HG01515.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(20): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(11): Show |
G | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-190-16492_-190-16 others(24): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621605 | GTCTTTTT others(12): Show |
G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(25): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | ||||||
| chr17:2621607 | C | T | 1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-190-16492C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621607 | |||||||
| chr17:2621607 | CT | C | 23 | a0001c0001t0001g0021 a0001c0001t0001g0060 a0001c0001t0001g0064 others(20): Show |
23 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-16456delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTT | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(22): Show |
25 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-190-16457_-190-16 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTTT | C | 20 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(17): Show |
20 | HG00597.hp2 HG01099.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.-190-16458_-190-16 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0005g0004 a0001c0001t0005g0086 a0001c0001t0005g0091 |
3 | HG02074.hp1 HG02165.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-190-16467_-190-16 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0002g0080 a0001c0001t0005g0081 |
2 | HG01123.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-190-16469_-190-16 others(20): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTTTTTTT others(8): Show |
C | 40 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0079 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.-190-16470_-190-16 others(21): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0174 a0001c0001t0002g0169 others(1): Show |
4 | HG02896.hp2 NA18947.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-16471_-190-16 others(22): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-190-16473_-190-16 others(24): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621607 | CTTTTTTT others(12): Show |
C | 26 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(23): Show |
26 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-16474_-190-16 others(25): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | ||||||
| chr17:2621619 | T | G | 1 | a0001c0001t0002g0234 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-190-16480T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621619 | |||||||
| chr17:2621627 | T | G | 1 | a0001c0001t0002g0122 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-190-16472T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621627 | |||||||
| chr17:2621633 | T | C | 1 | a0001c0001t0003g0278 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-190-16466T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621633 | |||||||
| chr17:2621665 | G | A | 5 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0122 others(2): Show |
5 | HG02015.hp1 NA18612.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-16434G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621665 | |||||||
| chr17:2621719 | A | G | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
122 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.-190-16380A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621719 | |||||||
| chr17:2621745 | C | G | 4 | a0001c0001t0003g0217 a0001c0001t0013g0218 a0001c0001t0013g0253 others(1): Show |
4 | HG03453.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-16354C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621745 | |||||||
| chr17:2621881 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(57): Show |
60 | HG00438.hp2 HG00733.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.-190-16218T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621881 | |||||||
| chr17:2621949 | TATTAC | T | 8 | a0001c0001t0023g0135 a0001c0002t0006g0185 a0001c0002t0006g0186 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-190-16146_-190-16 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621949 | ||||||
| chr17:2622163 | A | G | 5 | a0001c0001t0002g0234 a0001c0001t0011g0239 a0001c0001t0011g0240 others(2): Show |
5 | HG01993.hp2 HG02004.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-15936A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622163 | |||||||
| chr17:2622234 | G | A | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-15865G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622234 | |||||||
| chr17:2622801 | G | C | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG00099.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-190-15298G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622801 | |||||||
| chr17:2622927 | C | T | 3 | a0001c0001t0002g0037 a0001c0001t0002g0056 a0001c0001t0002g0156 |
3 | NA18944.hp2 NA18952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-190-15172C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622927 | |||||||
| chr17:2622987 | C | G | 1 | a0001c0001t0035g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-190-15112C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622987 | |||||||
| chr17:2623010 | A | G | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-190-15089A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623010 | |||||||
| chr17:2623040 | A | G | 1 | a0001c0001t0029g0182 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-190-15059A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623040 | |||||||
| chr17:2623079 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-190-15020A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623079 | |||||||
| chr17:2623181 | A | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-14918A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623181 | |||||||
| chr17:2623261 | CT | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
153 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-190-14816delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623261 | ||||||
| chr17:2623261 | CTT | C | 75 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0216 others(72): Show |
75 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-190-14817_-190-14 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623261 | ||||||
| chr17:2623266 | T | C | 6 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-190-14833T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623266 | |||||||
| chr17:2623267 | T | C | 1 | a0001c0002t0006g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-190-14832T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623267 | |||||||
| chr17:2623267 | T | G | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-190-14832T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623267 | |||||||
| chr17:2623283 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-190-14816T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623283 | |||||||
| chr17:2623308 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-190-14791C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623308 | |||||||
| chr17:2623460 | A | G | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
119 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-14639A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623460 | |||||||
| chr17:2623473 | TGGTC | T | 6 | a0001c0001t0023g0135 a0001c0003t0010g0175 a0001c0003t0010g0176 others(3): Show |
6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-190-14625_-190-14 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623473 | |||||||
| chr17:2623630 | G | GT | 16 | a0001c0001t0002g0084 a0001c0001t0008g0138 a0001c0001t0008g0140 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-190-14455dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623630 | ||||||
| chr17:2623752 | A | AGGTAGCT others(14): Show |
51 | a0001c0001t0002g0234 a0001c0001t0003g0217 a0001c0001t0003g0225 others(48): Show |
51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.-190-14346_-190-14 others(27): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623752 | ||||||
| chr17:2623752 | A | AGGTAGCT others(35): Show |
1 | a0001c0001t0009g0057 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-190-14326_-190-14 others(48): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623752 | ||||||
| chr17:2623770 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0160 |
2 | NA18960.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-190-14329C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623770 | |||||||
| chr17:2623774 | A | G | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0216 others(69): Show |
72 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-14325A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623774 | |||||||
| chr17:2624027 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-190-14072A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624027 | |||||||
| chr17:2624144 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-13955G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624144 | |||||||
| chr17:2624373 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0153 |
2 | HG00642.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190-13726C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624373 | |||||||
| chr17:2624646 | G | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
118 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.-190-13453G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624646 | |||||||
| chr17:2624660 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-190-13439G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624660 | |||||||
| chr17:2624734 | G | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0002g0115 |
3 | HG00544.hp2 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-190-13365G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624734 | |||||||
| chr17:2624901 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-190-13198A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624901 | |||||||
| chr17:2625023 | A | AT | 53 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0128 others(50): Show |
53 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-190-13063dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2625023 | ||||||
| chr17:2625062 | G | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-13037G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625062 | |||||||
| chr17:2625111 | T | C | 1 | a0001c0001t0030g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-190-12988T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625111 | |||||||
| chr17:2625537 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(3): Show |
6 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-190-12562A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625537 | |||||||
| chr17:2625541 | C | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-12558C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625541 | |||||||
| chr17:2625673 | C | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-12426C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625673 | |||||||
| chr17:2625706 | G | T | 76 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0216 others(73): Show |
76 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-190-12393G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625706 | |||||||
| chr17:2625966 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(14): Show |
17 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190-12133A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625966 | |||||||
| chr17:2626015 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-190-12084C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626015 | |||||||
| chr17:2626104 | T | A | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.-190-11995T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626104 | |||||||
| chr17:2626143 | A | G | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-11956A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626143 | |||||||
| chr17:2626259 | A | G | 75 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0216 others(72): Show |
75 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-190-11840A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626259 | |||||||
| chr17:2626294 | G | A | 76 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0216 others(73): Show |
76 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-190-11805G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626294 | |||||||
| chr17:2626385 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-190-11714G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626385 | |||||||
| chr17:2626493 | T | C | 1 | a0001c0001t0009g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-190-11606T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626493 | |||||||
| chr17:2626553 | T | TC | 25 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(22): Show |
25 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-190-11528dupC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | T | TCC | 28 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0032 others(25): Show |
28 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-190-11529_-190-11 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | T | TCCC | 17 | a0001c0001t0001g0060 a0001c0001t0001g0070 a0001c0001t0001g0114 others(14): Show |
17 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-190-11530_-190-11 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | T | TCCCC | 17 | a0001c0001t0001g0021 a0001c0001t0002g0111 a0001c0001t0004g0250 others(14): Show |
17 | HG00438.hp1 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190-11531_-190-11 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | T | TCCCCCCC others(4): Show |
2 | a0001c0001t0001g0040 a0001c0001t0030g0106 |
2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-190-11538_-190-11 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | T | TCCCCCCC others(5): Show |
1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-11539_-190-11 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | TC | T | 23 | a0001c0001t0001g0039 a0001c0001t0001g0075 a0001c0001t0001g0112 others(20): Show |
23 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-11528delC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | TCC | T | 19 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0002g0037 others(16): Show |
19 | HG00558.hp1 HG00733.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-190-11529_-190-11 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626553 | TCCC | T | 21 | a0001c0001t0001g0184 a0001c0001t0002g0207 a0001c0001t0013g0218 others(18): Show |
21 | HG00099.hp2 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-190-11530_-190-11 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | ||||||
| chr17:2626558 | C | CCCG | 13 | a0001c0001t0003g0261 a0001c0001t0003g0265 a0001c0001t0003g0269 others(10): Show |
13 | HG01978.hp1 HG02055.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190-11539_-190-11 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626558 | ||||||
| chr17:2626559 | C | CCG | 17 | a0001c0001t0003g0002 a0001c0001t0003g0221 a0001c0001t0003g0222 others(14): Show |
17 | HG01070.hp1 HG01255.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.-190-11539_-190-11 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626559 | ||||||
| chr17:2626560 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-190-11539C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626560 | |||||||
| chr17:2626560 | C | CG | 18 | a0001c0001t0003g0254 a0001c0001t0003g0255 a0001c0001t0003g0259 others(15): Show |
18 | HG00733.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-190-11539_-190-11 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626560 | |||||||
| chr17:2626561 | C | G | 11 | a0001c0001t0001g0123 a0001c0001t0002g0234 a0001c0001t0004g0198 others(8): Show |
11 | HG01074.hp1 HG02155.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-190-11538C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626561 | |||||||
| chr17:2626563 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-190-11536C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626563 | |||||||
| chr17:2626564 | C | T | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-11535C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626564 | |||||||
| chr17:2626566 | C | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01168.hp1 HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-190-11533C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626566 | |||||||
| chr17:2626571 | C | T | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-11528C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626571 | |||||||
| chr17:2626572 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-190-11527G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626572 | |||||||
| chr17:2626624 | G | A | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-190-11475G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626624 | |||||||
| chr17:2626640 | T | C | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
124 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(121): Show |
intron_variant | MODIFIER | c.-190-11459T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626640 | |||||||
| chr17:2626643 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-11456C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626643 | |||||||
| chr17:2626756 | T | C | 1 | a0001c0001t0011g0233 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-190-11343T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626756 | |||||||
| chr17:2626781 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-11318C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626781 | |||||||
| chr17:2626799 | C | T | 1 | a0001c0002t0006g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-190-11300C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626799 | |||||||
| chr17:2627061 | T | A | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-190-11038T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627061 | |||||||
| chr17:2627314 | G | T | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-10785G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627314 | |||||||
| chr17:2627516 | G | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-10583G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627516 | |||||||
| chr17:2627555 | C | G | 1 | a0001c0001t0005g0086 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-190-10544C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627555 | |||||||
| chr17:2627584 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-190-10515G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627584 | |||||||
| chr17:2627834 | G | C | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-10265G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627834 | |||||||
| chr17:2627977 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-190-10122G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627977 | |||||||
| chr17:2628081 | T | A | 26 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(23): Show |
26 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-10018T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628081 | |||||||
| chr17:2628123 | G | A | 1 | a0001c0001t0011g0270 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-190-9976G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628123 | |||||||
| chr17:2628157 | G | A | 1 | a0001c0001t0035g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-190-9942G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628157 | |||||||
| chr17:2628195 | T | C | 2 | a0001c0001t0002g0073 a0001c0001t0002g0157 |
2 | NA18979.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-190-9904T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628195 | |||||||
| chr17:2628219 | A | G | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-190-9880A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628219 | |||||||
| chr17:2628296 | T | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-190-9803T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628296 | |||||||
| chr17:2628505 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-9594T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628505 | |||||||
| chr17:2628657 | G | T | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-9442G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628657 | |||||||
| chr17:2628758 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
73 | HG00558.hp2 HG00735.hp1 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.-190-9341G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628758 | |||||||
| chr17:2628852 | T | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
119 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-9247T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628852 | |||||||
| chr17:2628978 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-9121T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628978 | |||||||
| chr17:2629049 | ATTTATCT | A | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-9046_-190-904 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2629049 | ||||||
| chr17:2629473 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-190-8626C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629473 | |||||||
| chr17:2629571 | G | A | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-8528G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629571 | |||||||
| chr17:2629583 | A | G | 27 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0229 others(24): Show |
27 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-190-8516A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629583 | |||||||
| chr17:2629624 | C | T | 1 | a0001c0002t0006g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-190-8475C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629624 | |||||||
| chr17:2630206 | A | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-7893A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630206 | |||||||
| chr17:2630276 | G | A | 76 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(73): Show |
76 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-190-7823G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630276 | |||||||
| chr17:2630281 | GCAGTTCT others(649): Show |
G | 1 | a0001c0001t0002g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-190-7813_-190-715 others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2630281 | ||||||
| chr17:2630329 | G | C | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-7770G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630329 | |||||||
| chr17:2630394 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-190-7705C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630394 | |||||||
| chr17:2630426 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-7673G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630426 | |||||||
| chr17:2630553 | G | A | 1 | a0001c0005t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-190-7546G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630553 | |||||||
| chr17:2630780 | C | T | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-7319C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630780 | |||||||
| chr17:2631059 | G | C | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-190-7040G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631059 | |||||||
| chr17:2631361 | G | A | 1 | a0001c0001t0034g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-190-6738G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631361 | |||||||
| chr17:2631416 | A | G | 11 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0126 others(8): Show |
11 | HG00642.hp2 HG02015.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-190-6683A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631416 | |||||||
| chr17:2631527 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-190-6572C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631527 | |||||||
| chr17:2631624 | G | T | 5 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0235 others(2): Show |
5 | HG01255.hp2 HG01257.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-6475G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631624 | |||||||
| chr17:2631643 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-190-6456A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631643 | |||||||
| chr17:2631666 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-190-6433C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631666 | |||||||
| chr17:2631669 | C | T | 3 | a0001c0001t0005g0058 a0001c0001t0005g0078 a0001c0001t0005g0092 |
3 | HG00597.hp2 HG03927.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-190-6430C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631669 | |||||||
| chr17:2631676 | G | A | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-190-6423G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631676 | |||||||
| chr17:2631683 | A | G | 1 | a0001c0003t0010g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-190-6416A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631683 | |||||||
| chr17:2631983 | A | G | 2 | a0001c0001t0007g0213 a0001c0001t0007g0274 |
2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-190-6116A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631983 | |||||||
| chr17:2632026 | T | C | 122 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
122 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(119): Show |
intron_variant | MODIFIER | c.-190-6073T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632026 | |||||||
| chr17:2632160 | C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-5939C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632160 | |||||||
| chr17:2632353 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-190-5746G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632353 | |||||||
| chr17:2632432 | C | G | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-5667C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632432 | |||||||
| chr17:2632573 | G | T | 77 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(74): Show |
77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-190-5526G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632573 | |||||||
| chr17:2632584 | C | T | 7 | a0001c0001t0008g0137 a0001c0001t0008g0140 a0001c0001t0008g0141 others(4): Show |
7 | HG01167.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-5515C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632584 | |||||||
| chr17:2633148 | TTTTTTCT others(5): Show |
T | 1 | a0001c0001t0037g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-190-4941_-190-493 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633148 | ||||||
| chr17:2633175 | CT | C | 9 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0140 others(6): Show |
9 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-190-4912delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633175 | ||||||
| chr17:2633225 | T | A | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-4874T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633225 | |||||||
| chr17:2633337 | T | G | 2 | a0001c0001t0017g0010 a0001c0004t0036g0205 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-190-4762T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633337 | |||||||
| chr17:2633475 | C | CT | 28 | a0001c0001t0002g0062 a0001c0001t0002g0080 a0001c0001t0002g0083 others(25): Show |
28 | HG00558.hp2 HG00741.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-190-4611dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633475 | ||||||
| chr17:2633658 | C | A | 1 | a0001c0001t0012g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-190-4441C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633658 | |||||||
| chr17:2633788 | T | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
119 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-4311T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633788 | |||||||
| chr17:2633889 | G | A | 1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-190-4210G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633889 | |||||||
| chr17:2633920 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-4179C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633920 | |||||||
| chr17:2633961 | C | CT | 22 | a0001c0001t0001g0094 a0001c0001t0002g0037 a0001c0001t0002g0080 others(19): Show |
22 | HG00597.hp2 HG01123.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-190-4116dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | ||||||
| chr17:2633961 | C | CTT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0105 a0001c0001t0002g0089 others(6): Show |
9 | HG00323.hp1 HG00323.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-190-4117_-190-411 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | ||||||
| chr17:2633961 | CT | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(35): Show |
38 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.-190-4116delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | ||||||
| chr17:2633961 | CTT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0184 a0001c0001t0012g0279 others(9): Show |
12 | HG01891.hp1 HG02647.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.-190-4117_-190-411 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | ||||||
| chr17:2633961 | CTTTT | C | 71 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(68): Show |
71 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-190-4119_-190-411 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | ||||||
| chr17:2633961 | CTTTTT | C | 7 | a0001c0001t0003g0277 a0001c0001t0004g0228 a0001c0001t0004g0229 others(4): Show |
7 | HG01257.hp2 HG01261.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-4120_-190-411 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | ||||||
| chr17:2633997 | G | A | 77 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(74): Show |
77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-190-4102G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633997 | |||||||
| chr17:2634159 | G | A | 7 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0071 others(4): Show |
7 | NA18943.hp2 NA18951.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-3940G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634159 | |||||||
| chr17:2634207 | C | A | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-3892C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634207 | |||||||
| chr17:2634257 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-3842C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634257 | |||||||
| chr17:2634323 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-190-3776G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634323 | |||||||
| chr17:2634425 | C | T | 1 | a0001c0001t0012g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-190-3674C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634425 | |||||||
| chr17:2634608 | C | A | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-3491C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634608 | |||||||
| chr17:2634673 | T | C | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-3426T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634673 | |||||||
| chr17:2634754 | T | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-3345T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634754 | |||||||
| chr17:2634854 | T | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-3245T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634854 | |||||||
| chr17:2634902 | G | C | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-3197G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634902 | |||||||
| chr17:2634979 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-190-3120A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634979 | |||||||
| chr17:2634991 | C | G | 1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-190-3108C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634991 | |||||||
| chr17:2635121 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-190-2978C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635121 | |||||||
| chr17:2635124 | G | C | 77 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(74): Show |
77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-190-2975G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635124 | |||||||
| chr17:2635126 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-190-2973G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635126 | |||||||
| chr17:2635184 | A | C | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-2915A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635184 | |||||||
| chr17:2635219 | G | C | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-2880G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635219 | |||||||
| chr17:2635515 | G | A | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0016 |
3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-190-2584G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635515 | |||||||
| chr17:2635646 | A | C | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-2453A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635646 | |||||||
| chr17:2635667 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-190-2432T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635667 | |||||||
| chr17:2635760 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-190-2339G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635760 | |||||||
| chr17:2635820 | G | A | 1 | a0001c0001t0027g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-190-2279G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635820 | |||||||
| chr17:2635934 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-190-2165C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635934 | |||||||
| chr17:2635953 | C | CA | 14 | a0001c0001t0001g0052 a0001c0001t0003g0217 a0001c0001t0003g0265 others(11): Show |
14 | HG01261.hp1 HG01884.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190-2126dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | ||||||
| chr17:2635953 | CA | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(21): Show |
24 | HG00099.hp1 HG01099.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-190-2126delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | ||||||
| chr17:2635953 | CAA | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(12): Show |
15 | HG00099.hp2 HG01123.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-2127_-190-212 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | ||||||
| chr17:2635953 | CAAA | C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0128 others(33): Show |
36 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.-190-2128_-190-212 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | ||||||
| chr17:2635984 | T | A | 1 | a0001c0001t0005g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-190-2115T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635984 | |||||||
| chr17:2636124 | T | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-1975T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636124 | |||||||
| chr17:2636235 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-1864A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636235 | |||||||
| chr17:2636327 | G | A | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-1772G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636327 | |||||||
| chr17:2636405 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-1694T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636405 | |||||||
| chr17:2636664 | G | A | 1 | a0001c0001t0042g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-190-1435G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636664 | |||||||
| chr17:2636690 | C | T | 3 | a0001c0001t0010g0181 a0001c0001t0021g0180 a0001c0001t0022g0183 |
3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-190-1409C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636690 | |||||||
| chr17:2636691 | G | A | 1 | a0001c0001t0004g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190-1408G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636691 | |||||||
| chr17:2636817 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-1282G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636817 | |||||||
| chr17:2636921 | G | A | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-1178G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636921 | |||||||
| chr17:2637240 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-190-859A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637240 | |||||||
| chr17:2637263 | G | A | 3 | a0001c0001t0012g0279 a0001c0001t0015g0280 a0001c0001t0042g0015 |
3 | HG03225.hp2 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-190-836G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637263 | |||||||
| chr17:2637416 | CA | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
226 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.-190-673delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2637416 | ||||||
| chr17:2637474 | C | T | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-190-625C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637474 | |||||||
| chr17:2637666 | T | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-433T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637666 | |||||||
| chr17:2637848 | A | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-251A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637848 | |||||||
| chr17:2637916 | T | C | 1 | a0001c0001t0031g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-190-183T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637916 | |||||||
| chr17:2637973 | AATC | A | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-119_-190-117d others(5): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2637973 | ||||||
| chr17:2638386 | A | T | 1 | a0001c0001t0002g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32+66A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638386 | |||||||
| chr17:2638667 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+347C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638667 | |||||||
| chr17:2638798 | T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+478T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638798 | |||||||
| chr17:2638844 | A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+524A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638844 | |||||||
| chr17:2638897 | C | CTTATTT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+592_32+597dupAT others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2638897 | ||||||
| chr17:2638928 | C | T | 2 | a0001c0001t0008g0137 a0001c0001t0008g0142 |
2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+608C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638928 | |||||||
| chr17:2638930 | C | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+610C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638930 | |||||||
| chr17:2638960 | C | T | 18 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.32+640C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638960 | |||||||
| chr17:2639018 | A | G | 1 | a0001c0001t0007g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.32+698A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639018 | |||||||
| chr17:2639603 | C | CT | 18 | a0001c0001t0003g0011 a0001c0001t0003g0099 a0001c0001t0008g0137 others(15): Show |
18 | HG00558.hp2 HG01109.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.32+1294dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2639603 | ||||||
| chr17:2639656 | G | T | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+1336G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639656 | |||||||
| chr17:2639676 | A | G | 1 | a0001c0001t0011g0242 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.32+1356A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639676 | |||||||
| chr17:2639844 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.32+1524C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639844 | |||||||
| chr17:2639887 | C | A | 3 | a0001c0001t0002g0062 a0001c0001t0002g0083 a0001c0001t0002g0120 |
3 | HG00741.hp2 HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.32+1567C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639887 | |||||||
| chr17:2640139 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.32+1819T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640139 | |||||||
| chr17:2640167 | C | A | 93 | a0001c0001t0001g0184 a0001c0001t0002g0234 a0001c0001t0003g0002 others(90): Show |
93 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+1847C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640167 | |||||||
| chr17:2640375 | C | CT | 19 | a0001c0001t0001g0006 a0001c0001t0001g0184 a0001c0001t0002g0206 others(16): Show |
19 | HG00733.hp2 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.32+2071dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640375 | ||||||
| chr17:2640375 | C | CTT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+2070_32+2071dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640375 | ||||||
| chr17:2640375 | CT | C | 78 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0067 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+2071delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640375 | ||||||
| chr17:2640412 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+2092A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640412 | |||||||
| chr17:2640451 | C | CT | 19 | a0001c0001t0001g0046 a0001c0001t0001g0071 a0001c0001t0002g0111 others(16): Show |
19 | HG00438.hp1 HG00544.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.32+2149dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640451 | ||||||
| chr17:2640451 | C | CTT | 10 | a0001c0001t0001g0184 a0001c0001t0021g0180 a0001c0001t0022g0183 others(7): Show |
10 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+2148_32+2149dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640451 | ||||||
| chr17:2640602 | C | G | 5 | a0001c0001t0002g0234 a0001c0001t0011g0239 a0001c0001t0011g0240 others(2): Show |
5 | HG01993.hp2 HG02004.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+2282C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640602 | |||||||
| chr17:2640602 | C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+2282C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640602 | |||||||
| chr17:2640926 | G | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+2606G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640926 | |||||||
| chr17:2641083 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+2763T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641083 | |||||||
| chr17:2641091 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0157 |
2 | NA18979.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.32+2771C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641091 | |||||||
| chr17:2641186 | A | G | 1 | a0001c0001t0002g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.32+2866A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641186 | |||||||
| chr17:2641261 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+2941C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641261 | |||||||
| chr17:2641430 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32+3110A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641430 | |||||||
| chr17:2641443 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.32+3123G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641443 | |||||||
| chr17:2641452 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.32+3132C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641452 | |||||||
| chr17:2641669 | T | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+3349T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641669 | |||||||
| chr17:2641755 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+3435C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641755 | |||||||
| chr17:2641868 | C | G | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+3548C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641868 | |||||||
| chr17:2642079 | T | C | 4 | a0001c0001t0002g0073 a0001c0001t0002g0104 a0001c0001t0002g0157 others(1): Show |
4 | HG04184.hp1 NA18979.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+3759T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642079 | |||||||
| chr17:2642179 | A | G | 35 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(32): Show |
35 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.32+3859A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642179 | |||||||
| chr17:2642377 | T | G | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+4057T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642377 | |||||||
| chr17:2642417 | T | A | 1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.32+4097T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642417 | |||||||
| chr17:2642696 | G | A | 1 | a0001c0001t0026g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.32+4376G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642696 | |||||||
| chr17:2642907 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
4 | HG01243.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+4587A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642907 | |||||||
| chr17:2642968 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.32+4648C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642968 | |||||||
| chr17:2643039 | A | G | 3 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0032g0197 |
3 | HG01070.hp1 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.32+4719A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643039 | |||||||
| chr17:2643046 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(42): Show |
45 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.32+4726C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643046 | |||||||
| chr17:2643047 | CTCTT | C | 4 | a0001c0001t0004g0244 a0001c0001t0004g0247 a0001c0001t0004g0250 others(1): Show |
4 | HG01168.hp2 HG02486.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+4732_32+4735del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2643047 | ||||||
| chr17:2643112 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.32+4792G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643112 | |||||||
| chr17:2643155 | T | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+4835T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643155 | |||||||
| chr17:2643171 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.32+4851C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643171 | |||||||
| chr17:2643307 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.32+4987C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643307 | |||||||
| chr17:2643319 | A | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+4999A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643319 | |||||||
| chr17:2643489 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.32+5169C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643489 | |||||||
| chr17:2643554 | CT | C | 93 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0001g0174 others(90): Show |
93 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.32+5246delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2643554 | ||||||
| chr17:2643613 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32+5293G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643613 | |||||||
| chr17:2643797 | C | G | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+5477C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643797 | |||||||
| chr17:2643862 | C | A | 1 | a0001c0001t0005g0097 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.32+5542C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643862 | |||||||
| chr17:2644118 | C | T | 77 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(74): Show |
77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.32+5798C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644118 | |||||||
| chr17:2644171 | T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+5851T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644171 | |||||||
| chr17:2644377 | A | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0134 a0001c0001t0001g0147 others(2): Show |
5 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+6057A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644377 | |||||||
| chr17:2644474 | C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+6154C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644474 | |||||||
| chr17:2644529 | G | A | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+6209G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644529 | |||||||
| chr17:2644902 | A | G | 1 | a0001c0001t0003g0255 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.32+6582A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644902 | |||||||
| chr17:2645075 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.32+6755C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645075 | |||||||
| chr17:2645146 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.32+6826C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645146 | |||||||
| chr17:2645319 | C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+6999C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645319 | |||||||
| chr17:2645550 | A | G | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+7230A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645550 | |||||||
| chr17:2645607 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32+7287T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645607 | |||||||
| chr17:2645609 | A | T | 1 | a0001c0001t0005g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.32+7289A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645609 | |||||||
| chr17:2645623 | A | T | 21 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(18): Show |
21 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+7303A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645623 | |||||||
| chr17:2645992 | T | A | 1 | a0001c0001t0003g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.32+7672T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645992 | |||||||
| chr17:2646198 | T | C | 2 | a0001c0001t0012g0013 a0001c0001t0012g0016 |
2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.32+7878T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2646198 | |||||||
| chr17:2646436 | TGAGGTCA others(3): Show |
T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.32+8118_32+8127del others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2646436 | ||||||
| chr17:2646652 | TAATAA | T | 4 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0224 others(1): Show |
4 | NA18946.hp1 NA18979.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+8339_32+8343del others(5): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2646652 | ||||||
| chr17:2646951 | G | T | 1 | a0001c0001t0013g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.32+8631G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2646951 | |||||||
| chr17:2646982 | A | G | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+8662A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2646982 | |||||||
| chr17:2647121 | A | G | 27 | a0001c0001t0001g0128 a0001c0001t0001g0154 a0001c0001t0002g0037 others(24): Show |
27 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+8801A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647121 | |||||||
| chr17:2647213 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.32+8893C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647213 | |||||||
| chr17:2647282 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.32+8962C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647282 | |||||||
| chr17:2647302 | G | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+8982G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647302 | |||||||
| chr17:2647305 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.32+8985G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647305 | |||||||
| chr17:2647659 | A | G | 1 | a0001c0001t0041g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.32+9339A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647659 | |||||||
| chr17:2647964 | G | A | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+9644G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647964 | |||||||
| chr17:2648146 | A | G | 2 | a0001c0001t0003g0256 a0001c0001t0003g0263 |
2 | NA18968.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.32+9826A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648146 | |||||||
| chr17:2648147 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.32+9827T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648147 | |||||||
| chr17:2648246 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.32+9926G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648246 | |||||||
| chr17:2648419 | G | A | 1 | a0001c0001t0031g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+10099G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648419 | |||||||
| chr17:2648468 | A | G | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+10148A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648468 | |||||||
| chr17:2648532 | G | T | 1 | a0001c0001t0038g0238 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.32+10212G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648532 | |||||||
| chr17:2648533 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0002g0118 |
2 | HG00544.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.32+10213C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648533 | |||||||
| chr17:2648653 | G | T | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+10333G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648653 | |||||||
| chr17:2648677 | C | CA | 51 | a0001c0001t0001g0067 a0001c0001t0002g0234 a0001c0001t0003g0217 others(48): Show |
51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+10373dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648677 | ||||||
| chr17:2648677 | CA | C | 7 | a0001c0001t0001g0114 a0001c0001t0003g0221 a0001c0001t0003g0222 others(4): Show |
7 | HG02074.hp2 HG02965.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+10373delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648677 | ||||||
| chr17:2648759 | G | GT | 87 | a0001c0001t0001g0145 a0001c0001t0002g0035 a0001c0001t0002g0053 others(84): Show |
87 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.32+10441dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648759 | ||||||
| chr17:2648762 | A | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.32+10442A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648762 | |||||||
| chr17:2648805 | C | T | 4 | a0001c0001t0002g0037 a0001c0001t0002g0056 a0001c0001t0002g0063 others(1): Show |
4 | HG00597.hp1 NA18944.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+10485C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648805 | |||||||
| chr17:2648925 | ATATT | A | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+10607_32+10610d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648925 | ||||||
| chr17:2649088 | G | A | 76 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(73): Show |
76 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.32+10768G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649088 | |||||||
| chr17:2649140 | CTG | C | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+10821_32+10822d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649140 | |||||||
| chr17:2649182 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.32+10862A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649182 | |||||||
| chr17:2649214 | C | CA | 21 | a0001c0001t0001g0052 a0001c0001t0001g0184 a0001c0001t0002g0111 others(18): Show |
21 | HG00438.hp1 HG01261.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.32+10912dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2649214 | ||||||
| chr17:2649214 | CA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+10912delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2649214 | ||||||
| chr17:2649598 | C | G | 4 | a0001c0001t0002g0062 a0001c0001t0002g0083 a0001c0001t0002g0120 others(1): Show |
4 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+11278C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649598 | |||||||
| chr17:2649858 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.32+11538A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649858 | |||||||
| chr17:2650271 | GGAGGCCG others(17): Show |
G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+11956_32+11979d others(26): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650271 | ||||||
| chr17:2650278 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+11958G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650278 | |||||||
| chr17:2650282 | C | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0079 others(39): Show |
42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.32+11962C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650282 | |||||||
| chr17:2650334 | A | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.32+12014A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650334 | |||||||
| chr17:2650436 | C | T | 1 | a0001c0001t0003g0254 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.32+12116C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650436 | |||||||
| chr17:2650507 | A | G | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+12187A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650507 | |||||||
| chr17:2650510 | T | TA | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
93 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.32+12206dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650510 | ||||||
| chr17:2650542 | G | A | 28 | a0001c0001t0001g0105 a0001c0001t0002g0080 a0001c0001t0005g0004 others(25): Show |
28 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.32+12222G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650542 | |||||||
| chr17:2650639 | CA | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.32+12340delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650639 | ||||||
| chr17:2650639 | CAAAAAAA others(1): Show |
C | 77 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(74): Show |
77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.32+12333_32+12340d others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650639 | ||||||
| chr17:2650770 | G | A | 72 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(69): Show |
72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+12450G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650770 | |||||||
| chr17:2650907 | A | G | 16 | a0001c0001t0004g0192 a0001c0001t0004g0229 a0001c0001t0004g0230 others(13): Show |
16 | HG00733.hp1 HG01168.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.32+12587A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650907 | |||||||
| chr17:2650908 | T | C | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+12588T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650908 | |||||||
| chr17:2650994 | G | A | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+12674G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650994 | |||||||
| chr17:2651036 | A | G | 78 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(75): Show |
78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+12716A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651036 | |||||||
| chr17:2651291 | T | G | 1 | a0001c0001t0004g0237 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.32+12971T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651291 | |||||||
| chr17:2651359 | C | T | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32+13039C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651359 | |||||||
| chr17:2651395 | G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+13075G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651395 | |||||||
| chr17:2651413 | C | CA | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(22): Show |
25 | HG00323.hp1 HG00597.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.32+13114dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2651413 | ||||||
| chr17:2651413 | CA | C | 36 | a0001c0001t0002g0153 a0001c0001t0003g0002 a0001c0001t0003g0099 others(33): Show |
36 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.32+13114delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2651413 | ||||||
| chr17:2651425 | A | G | 1 | a0001c0001t0009g0061 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.32+13105A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651425 | |||||||
| chr17:2651574 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+13254G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651574 | |||||||
| chr17:2651645 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.32+13325G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651645 | |||||||
| chr17:2651668 | CTTAAA | C | 79 | a0001c0001t0002g0234 a0001c0001t0003g0002 a0001c0001t0003g0099 others(76): Show |
79 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.32+13352_32+13356d others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2651668 | ||||||
| chr17:2651712 | T | C | 2 | a0001c0001t0014g0047 a0001c0001t0014g0048 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.32+13392T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651712 | |||||||
| chr17:2651760 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.32+13440C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651760 | |||||||
| chr17:2651937 | A | G | 27 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0229 others(24): Show |
27 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.33-13435A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651937 | |||||||
| chr17:2651941 | G | A | 37 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(34): Show |
37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-13431G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651941 | |||||||
| chr17:2651979 | C | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.33-13393C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651979 | |||||||
| chr17:2652058 | A | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.33-13314A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652058 | |||||||
| chr17:2652064 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.33-13308A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652064 | |||||||
| chr17:2652107 | A | G | 99 | a0001c0001t0001g0184 a0001c0001t0002g0234 a0001c0001t0003g0002 others(96): Show |
99 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.33-13265A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652107 | |||||||
| chr17:2652134 | A | G | 1 | a0001c0001t0031g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-13238A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652134 | |||||||
| chr17:2652150 | G | A | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13222G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652150 | |||||||
| chr17:2652161 | C | CA | 218 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.33-13210dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652161 | ||||||
| chr17:2652162 | A | AG | 13 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
13 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-13210_33-13209i others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652162 | |||||||
| chr17:2652177 | A | G | 51 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0051 others(48): Show |
51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.33-13195A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652177 | |||||||
| chr17:2652187 | A | G | 10 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(7): Show |
10 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-13185A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652187 | |||||||
| chr17:2652193 | G | T | 58 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(55): Show |
58 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.33-13179G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652193 | |||||||
| chr17:2652204 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.33-13168A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652204 | |||||||
| chr17:2652206 | C | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.33-13166C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652206 | |||||||
| chr17:2652207 | G | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
75 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.33-13165G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652207 | |||||||
| chr17:2652213 | A | G | 37 | a0001c0001t0001g0113 a0001c0001t0001g0184 a0001c0001t0002g0158 others(34): Show |
37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-13159A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652213 | |||||||
| chr17:2652215 | C | T | 1 | a0001c0001t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33-13157C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652215 | |||||||
| chr17:2652216 | C | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.33-13156C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652216 | |||||||
| chr17:2652217 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.33-13155T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652217 | |||||||
| chr17:2652224 | C | A | 2 | a0001c0001t0010g0181 a0001c0001t0021g0180 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-13148C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652224 | |||||||
| chr17:2652226 | C | T | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
33 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.33-13146C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652226 | |||||||
| chr17:2652268 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-13104G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652268 | |||||||
| chr17:2652275 | C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-13097C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652275 | |||||||
| chr17:2652276 | G | A | 51 | a0001c0001t0001g0171 a0001c0001t0001g0184 a0001c0001t0002g0234 others(48): Show |
51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.33-13096G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652276 | |||||||
| chr17:2652282 | G | A | 6 | a0001c0001t0023g0135 a0001c0003t0010g0175 a0001c0003t0010g0176 others(3): Show |
6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-13090G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652282 | |||||||
| chr17:2652283 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-13089C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652283 | |||||||
| chr17:2652283 | CG | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-13086delG | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652283 | ||||||
| chr17:2652287 | T | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.33-13085T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652287 | |||||||
| chr17:2652294 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-13078A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652294 | |||||||
| chr17:2652298 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0025 others(46): Show |
49 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.33-13074C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652298 | |||||||
| chr17:2652337 | C | A | 6 | a0001c0001t0002g0080 a0001c0001t0005g0097 a0001c0001t0005g0098 others(3): Show |
6 | HG01123.hp2 HG01934.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13035C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652337 | |||||||
| chr17:2652356 | A | C | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-13016A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652356 | |||||||
| chr17:2652364 | A | G | 5 | a0001c0001t0003g0225 a0001c0001t0003g0227 a0001c0001t0013g0218 others(2): Show |
5 | HG02809.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-13008A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652364 | |||||||
| chr17:2652374 | C | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-12998C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652374 | |||||||
| chr17:2652377 | T | C | 2 | a0001c0001t0004g0243 a0001c0001t0004g0248 |
2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.33-12995T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652377 | |||||||
| chr17:2652395 | G | A | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-12977G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652395 | |||||||
| chr17:2652402 | G | A | 6 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(3): Show |
6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-12970G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652402 | |||||||
| chr17:2652414 | C | CAAACA | 3 | a0001c0001t0010g0181 a0001c0001t0021g0180 a0001c0001t0022g0183 |
3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-12944_33-12940d others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652414 | ||||||
| chr17:2652421 | A | AC | 4 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0224 others(1): Show |
4 | NA18946.hp1 NA18979.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-12951_33-12950i others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652421 | |||||||
| chr17:2652423 | C | A | 4 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0224 others(1): Show |
4 | NA18946.hp1 NA18979.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-12949C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652423 | |||||||
| chr17:2652429 | A | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-12943A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652429 | |||||||
| chr17:2652576 | A | AT | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
101 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.33-12795dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652576 | ||||||
| chr17:2652832 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.33-12540A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652832 | |||||||
| chr17:2652842 | T | C | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-12530T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652842 | |||||||
| chr17:2652986 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-12386C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652986 | |||||||
| chr17:2653019 | C | T | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-12353C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653019 | |||||||
| chr17:2653180 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.33-12192A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653180 | |||||||
| chr17:2653332 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.33-12040A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653332 | |||||||
| chr17:2653418 | T | TA | 37 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0002g0234 others(34): Show |
37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-11942dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2653418 | ||||||
| chr17:2653418 | TA | T | 34 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
34 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.33-11942delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2653418 | ||||||
| chr17:2653668 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.33-11704G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653668 | |||||||
| chr17:2653673 | C | T | 44 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0079 others(41): Show |
44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.33-11699C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653673 | |||||||
| chr17:2653677 | T | C | 37 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(34): Show |
37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-11695T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653677 | |||||||
| chr17:2653806 | T | A | 18 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.33-11566T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653806 | |||||||
| chr17:2653953 | C | T | 159 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.33-11419C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653953 | |||||||
| chr17:2654045 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0160 |
2 | NA18960.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.33-11327G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654045 | |||||||
| chr17:2654112 | C | T | 41 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(38): Show |
41 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.33-11260C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654112 | |||||||
| chr17:2654154 | C | A | 18 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.33-11218C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654154 | |||||||
| chr17:2654369 | T | C | 4 | a0001c0001t0002g0062 a0001c0001t0002g0083 a0001c0001t0002g0120 others(1): Show |
4 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-11003T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654369 | |||||||
| chr17:2654421 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0085 |
3 | NA18943.hp2 NA19009.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.33-10951C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654421 | |||||||
| chr17:2654471 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.33-10901G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654471 | |||||||
| chr17:2654672 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
48 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-10700G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654672 | |||||||
| chr17:2654683 | C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-10689C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654683 | |||||||
| chr17:2654762 | C | G | 38 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(35): Show |
38 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.33-10610C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654762 | |||||||
| chr17:2654785 | G | A | 25 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(22): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-10587G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654785 | |||||||
| chr17:2654948 | T | C | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-10424T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654948 | |||||||
| chr17:2654954 | C | CT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-10404dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2654954 | ||||||
| chr17:2654954 | CT | C | 7 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0002g0084 others(4): Show |
7 | HG00099.hp2 HG01070.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-10404delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2654954 | ||||||
| chr17:2654969 | A | T | 17 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.33-10403A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654969 | |||||||
| chr17:2655047 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.33-10325G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655047 | |||||||
| chr17:2655048 | C | T | 1 | a0001c0001t0004g0232 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.33-10324C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655048 | |||||||
| chr17:2655099 | T | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.33-10273T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655099 | |||||||
| chr17:2655181 | A | ATGTG | 6 | a0001c0001t0002g0151 a0001c0003t0010g0175 a0001c0003t0010g0176 others(3): Show |
6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-10190_33-10189i others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655181 | ||||||
| chr17:2655181 | A | ATGTGTGT others(3): Show |
6 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0188 others(3): Show |
6 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-10190_33-10189i others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655181 | ||||||
| chr17:2655181 | A | ATGTGTGT others(5): Show |
1 | a0001c0002t0006g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-10190_33-10189i others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655181 | ||||||
| chr17:2655183 | A | ATG | 9 | a0001c0001t0001g0040 a0001c0001t0001g0079 a0001c0001t0002g0136 others(6): Show |
9 | HG00735.hp1 HG01516.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-10157_33-10156d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | ATGTG | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(5): Show |
8 | HG00438.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-10159_33-10156d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | ATGTGTG | 5 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0003g0225 others(2): Show |
5 | HG02717.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-10161_33-10156d others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | ATGTGTGT others(1): Show |
28 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(25): Show |
28 | HG00558.hp2 HG01346.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.33-10163_33-10156d others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | ATGTGTGT others(3): Show |
4 | a0001c0001t0003g0266 a0001c0001t0007g0213 a0001c0001t0007g0215 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-10165_33-10156d others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | ATGTGTGT others(5): Show |
3 | a0001c0001t0003g0222 a0001c0001t0003g0259 a0001c0001t0022g0183 |
3 | HG02258.hp1 NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.33-10167_33-10156d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0021g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.33-10169_33-10156d others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0010g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.33-10171_33-10156d others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | A | G | 17 | a0001c0001t0001g0184 a0001c0001t0002g0150 a0001c0001t0002g0151 others(14): Show |
17 | HG00558.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-10189A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655183 | |||||||
| chr17:2655183 | ATG | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
80 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.33-10157_33-10156d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0002g0234 a0001c0004t0036g0205 |
2 | HG02155.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-10165_33-10156d others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655183 | ATGTGTGT others(5): Show |
A | 5 | a0001c0001t0002g0108 a0001c0001t0002g0170 a0001c0001t0002g0194 others(2): Show |
5 | HG03453.hp1 HG03471.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-10167_33-10156d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | ||||||
| chr17:2655236 | G | A | 2 | a0001c0001t0004g0229 a0001c0001t0004g0237 |
2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.33-10136G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655236 | |||||||
| chr17:2655255 | A | G | 1 | a0001c0001t0009g0107 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33-10117A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655255 | |||||||
| chr17:2655490 | A | G | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-9882A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655490 | |||||||
| chr17:2655569 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-9803G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655569 | |||||||
| chr17:2655645 | G | A | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-9727G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655645 | |||||||
| chr17:2655679 | A | AT | 3 | a0001c0001t0002g0054 a0001c0001t0002g0122 a0001c0001t0002g0155 |
3 | HG02015.hp1 NA18943.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.33-9691dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655679 | ||||||
| chr17:2655762 | C | T | 25 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(22): Show |
25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-9610C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655762 | |||||||
| chr17:2655784 | G | GA | 7 | a0001c0001t0002g0037 a0001c0001t0002g0056 a0001c0001t0002g0063 others(4): Show |
7 | HG00597.hp1 HG01934.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-9575dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655784 | ||||||
| chr17:2655923 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0145 |
2 | HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.33-9449G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655923 | |||||||
| chr17:2655955 | C | T | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-9417C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655955 | |||||||
| chr17:2655986 | C | T | 14 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0045 others(11): Show |
14 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-9386C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655986 | |||||||
| chr17:2655988 | A | G | 1 | a0001c0001t0031g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-9384A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655988 | |||||||
| chr17:2656025 | T | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | HG00558.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.33-9347T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656025 | |||||||
| chr17:2656101 | T | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.33-9271T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656101 | |||||||
| chr17:2656145 | C | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 others(2): Show |
5 | HG00099.hp2 HG00733.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-9227C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656145 | |||||||
| chr17:2656255 | C | T | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.33-9117C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656255 | |||||||
| chr17:2656333 | C | T | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-9039C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656333 | |||||||
| chr17:2656368 | T | C | 1 | a0001c0001t0026g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-9004T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656368 | |||||||
| chr17:2656416 | C | A | 8 | a0001c0001t0002g0080 a0001c0001t0005g0097 a0001c0001t0005g0098 others(5): Show |
8 | HG01123.hp2 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-8956C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656416 | |||||||
| chr17:2656481 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.33-8891C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656481 | |||||||
| chr17:2656503 | A | C | 1 | a0001c0001t0004g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.33-8869A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656503 | |||||||
| chr17:2656589 | A | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(162): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.33-8783A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656589 | |||||||
| chr17:2656627 | C | T | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.33-8745C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656627 | |||||||
| chr17:2656871 | GTCTGTT | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.33-8491_33-8486del others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2656871 | ||||||
| chr17:2657022 | C | T | 1 | a0001c0001t0037g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33-8350C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657022 | |||||||
| chr17:2657137 | A | T | 38 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(35): Show |
38 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.33-8235A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657137 | |||||||
| chr17:2657304 | C | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.33-8068C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657304 | |||||||
| chr17:2657405 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-7967C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657405 | |||||||
| chr17:2657413 | A | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
66 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(63): Show |
intron_variant | MODIFIER | c.33-7959A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657413 | |||||||
| chr17:2657524 | G | A | 1 | a0001c0001t0026g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-7848G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657524 | |||||||
| chr17:2657601 | C | T | 1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-7771C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657601 | |||||||
| chr17:2657708 | C | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-7664C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657708 | |||||||
| chr17:2657875 | T | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(43): Show |
46 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-7497T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657875 | |||||||
| chr17:2658003 | T | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
48 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-7369T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658003 | |||||||
| chr17:2658204 | A | G | 1 | a0001c0001t0007g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.33-7168A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658204 | |||||||
| chr17:2658530 | A | C | 68 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(65): Show |
68 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-6842A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658530 | |||||||
| chr17:2658574 | C | T | 35 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(32): Show |
35 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-6798C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658574 | |||||||
| chr17:2658599 | A | G | 1 | a0001c0001t0004g0250 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.33-6773A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658599 | |||||||
| chr17:2658658 | C | T | 7 | a0001c0001t0001g0184 a0001c0001t0029g0182 a0001c0003t0010g0175 others(4): Show |
7 | HG01891.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-6714C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658658 | |||||||
| chr17:2658801 | T | G | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(43): Show |
46 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-6571T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658801 | |||||||
| chr17:2658859 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
48 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-6513G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658859 | |||||||
| chr17:2658946 | T | C | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33-6426T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658946 | |||||||
| chr17:2659184 | G | A | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-6188G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659184 | |||||||
| chr17:2659245 | CA | C | 41 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(38): Show |
41 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.33-6116delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2659245 | ||||||
| chr17:2659276 | C | T | 1 | a0001c0001t0004g0248 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.33-6096C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659276 | |||||||
| chr17:2659295 | T | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 |
3 | HG02257.hp1 HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.33-6077T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659295 | |||||||
| chr17:2659382 | C | G | 1 | a0001c0001t0002g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.33-5990C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659382 | |||||||
| chr17:2659430 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0002g0089 |
2 | HG00323.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.33-5942G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659430 | |||||||
| chr17:2659472 | G | T | 8 | a0001c0001t0007g0196 a0001c0001t0007g0213 a0001c0001t0007g0214 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-5900G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659472 | |||||||
| chr17:2659520 | C | CA | 34 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0069 others(31): Show |
34 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.33-5831dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2659520 | ||||||
| chr17:2659520 | C | CAA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-5832_33-5831dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2659520 | ||||||
| chr17:2659656 | C | A | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.33-5716C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659656 | |||||||
| chr17:2659722 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.33-5650A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659722 | |||||||
| chr17:2659916 | A | G | 167 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.33-5456A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659916 | |||||||
| chr17:2659967 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.33-5405T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659967 | |||||||
| chr17:2660127 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.33-5245C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660127 | |||||||
| chr17:2660176 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0002g0115 |
3 | HG00544.hp2 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.33-5196T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660176 | |||||||
| chr17:2660206 | C | CTTA | 48 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(45): Show |
48 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.33-5165_33-5163dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2660206 | ||||||
| chr17:2660225 | C | CT | 5 | a0001c0001t0002g0104 a0001c0001t0002g0165 a0001c0001t0003g0255 others(2): Show |
5 | HG00323.hp1 HG01255.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-5134dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2660225 | ||||||
| chr17:2660225 | CT | C | 5 | a0001c0001t0001g0060 a0001c0001t0002g0194 a0001c0001t0005g0152 others(2): Show |
5 | HG02622.hp2 HG02698.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-5134delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2660225 | ||||||
| chr17:2660238 | T | A | 1 | a0001c0001t0005g0058 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.33-5134T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660238 | |||||||
| chr17:2660349 | G | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
62 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(59): Show |
intron_variant | MODIFIER | c.33-5023G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660349 | |||||||
| chr17:2660453 | T | G | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.33-4919T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660453 | |||||||
| chr17:2660915 | C | T | 37 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(34): Show |
37 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-4457C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660915 | |||||||
| chr17:2660973 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(45): Show |
48 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.33-4399G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660973 | |||||||
| chr17:2660992 | C | G | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-4380C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660992 | |||||||
| chr17:2661043 | A | G | 1 | a0001c0001t0004g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.33-4329A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661043 | |||||||
| chr17:2661094 | G | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-4278G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661094 | |||||||
| chr17:2661191 | T | C | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-4181T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661191 | |||||||
| chr17:2661238 | T | C | 1 | a0001c0001t0022g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.33-4134T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661238 | |||||||
| chr17:2661614 | T | C | 277 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.33-3758T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661614 | |||||||
| chr17:2661715 | T | C | 37 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(34): Show |
37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-3657T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661715 | |||||||
| chr17:2661983 | G | A | 1 | a0001c0001t0007g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-3389G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661983 | |||||||
| chr17:2662005 | T | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.33-3367T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662005 | |||||||
| chr17:2662042 | C | CA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0046 others(47): Show |
50 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.33-3307dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662042 | ||||||
| chr17:2662042 | C | CAA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0075 a0001c0001t0001g0112 others(6): Show |
9 | HG00438.hp2 HG00738.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-3308_33-3307dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662042 | ||||||
| chr17:2662042 | CA | C | 40 | a0001c0001t0001g0147 a0001c0001t0002g0149 a0001c0001t0003g0002 others(37): Show |
40 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.33-3307delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662042 | ||||||
| chr17:2662180 | G | T | 3 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 |
3 | HG01884.hp1 HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.33-3192G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662180 | |||||||
| chr17:2662184 | G | C | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
66 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(63): Show |
intron_variant | MODIFIER | c.33-3188G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662184 | |||||||
| chr17:2662246 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.33-3126G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662246 | |||||||
| chr17:2662276 | C | T | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-3096C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662276 | |||||||
| chr17:2662343 | T | C | 15 | a0001c0001t0001g0184 a0001c0001t0023g0135 a0001c0001t0029g0182 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.33-3029T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662343 | |||||||
| chr17:2662378 | T | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0112 a0001c0001t0002g0054 |
3 | HG01169.hp1 HG01169.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.33-2994T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662378 | |||||||
| chr17:2662378 | T | TGTG | 4 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0002g0158 others(1): Show |
4 | HG01243.hp2 HG01433.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2994_33-2993ins others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662378 | |||||||
| chr17:2662378 | T | TTG | 49 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0025 others(46): Show |
49 | HG00609.hp2 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.33-2949_33-2948dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | T | TTGTG | 43 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0046 others(40): Show |
43 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.33-2951_33-2948dup others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | T | TTGTGTG | 22 | a0001c0001t0001g0039 a0001c0001t0001g0102 a0001c0001t0001g0105 others(19): Show |
22 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-2953_33-2948dup others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | T | TTGTGTGT others(1): Show |
13 | a0001c0001t0001g0109 a0001c0001t0001g0154 a0001c0001t0001g0161 others(10): Show |
13 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-2955_33-2948dup others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0002g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.33-2957_33-2948dup others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0002g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.33-2961_33-2948dup others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | TTG | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0070 others(14): Show |
17 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.33-2949_33-2948del others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | TTGTG | T | 37 | a0001c0001t0003g0002 a0001c0001t0003g0011 a0001c0001t0003g0099 others(34): Show |
37 | HG00558.hp2 HG00735.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-2951_33-2948del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | TTGTGTGT others(3): Show |
T | 21 | a0001c0001t0001g0184 a0001c0001t0004g0230 a0001c0001t0004g0231 others(18): Show |
21 | HG01255.hp2 HG01257.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-2957_33-2948del others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | TTGTGTGT others(5): Show |
T | 24 | a0001c0001t0001g0006 a0001c0001t0002g0234 a0001c0001t0003g0217 others(21): Show |
24 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-2959_33-2948del others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | TTGTGTGT others(7): Show |
T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-2961_33-2948del others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33-2963_33-2948del others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662378 | TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0164 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.33-2967_33-2948del others(20): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | ||||||
| chr17:2662419 | T | C | 1 | a0001c0003t0010g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.33-2953T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662419 | |||||||
| chr17:2662423 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-2949T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662423 | |||||||
| chr17:2662674 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.33-2698G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662674 | |||||||
| chr17:2662822 | C | T | 1 | a0001c0001t0005g0091 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.33-2550C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662822 | |||||||
| chr17:2662866 | T | G | 8 | a0001c0001t0010g0181 a0001c0001t0021g0180 a0001c0001t0022g0183 others(5): Show |
8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-2506T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662866 | |||||||
| chr17:2662868 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-2504T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662868 | |||||||
| chr17:2662957 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-2415T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662957 | |||||||
| chr17:2663081 | C | A | 59 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(56): Show |
59 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.33-2291C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663081 | |||||||
| chr17:2663113 | CTAAA | C | 4 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0032g0197 others(1): Show |
4 | HG01070.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2254_33-2251del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663113 | ||||||
| chr17:2663118 | TAAAG | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG01261.hp1 HG01516.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2244_33-2241del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663118 | ||||||
| chr17:2663472 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0220 |
2 | HG00738.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.33-1900C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663472 | |||||||
| chr17:2663556 | G | GTTC | 3 | a0001c0001t0002g0062 a0001c0001t0002g0083 a0001c0001t0002g0120 |
3 | HG00741.hp2 HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.33-1812_33-1810dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663556 | ||||||
| chr17:2663573 | TA | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.33-1797delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663573 | ||||||
| chr17:2663579 | A | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.33-1793A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663579 | |||||||
| chr17:2663594 | G | A | 1 | a0001c0001t0025g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.33-1778G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663594 | |||||||
| chr17:2663701 | A | AT | 216 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.33-1657dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663701 | ||||||
| chr17:2663701 | A | ATT | 14 | a0001c0001t0001g0164 a0001c0001t0002g0157 a0001c0001t0004g0248 others(11): Show |
14 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-1658_33-1657dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663701 | ||||||
| chr17:2663701 | A | ATTT | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-1659_33-1657dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663701 | ||||||
| chr17:2663720 | CAG | C | 31 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.33-1649_33-1648del others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663720 | ||||||
| chr17:2663808 | C | T | 1 | a0001c0001t0005g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.33-1564C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663808 | |||||||
| chr17:2663914 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.33-1458C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663914 | |||||||
| chr17:2663928 | C | T | 1 | a0001c0001t0005g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.33-1444C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663928 | |||||||
| chr17:2663975 | G | A | 1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.33-1397G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663975 | |||||||
| chr17:2664027 | G | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(34): Show |
37 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-1345G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664027 | |||||||
| chr17:2664032 | G | C | 2 | a0001c0001t0012g0012 a0001c0001t0015g0017 |
2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.33-1340G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664032 | |||||||
| chr17:2664193 | A | G | 1 | a0001c0001t0004g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33-1179A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664193 | |||||||
| chr17:2664407 | C | CT | 14 | a0001c0001t0001g0132 a0001c0001t0004g0192 a0001c0001t0004g0248 others(11): Show |
14 | HG00597.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-949dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664407 | ||||||
| chr17:2664407 | C | CTT | 7 | a0001c0002t0006g0185 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-950_33-949dupTT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664407 | ||||||
| chr17:2664407 | CT | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(43): Show |
46 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-949delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664407 | ||||||
| chr17:2664466 | T | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.33-906T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664466 | |||||||
| chr17:2664554 | T | G | 2 | a0001c0001t0004g0228 a0001c0001t0004g0252 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.33-818T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664554 | |||||||
| chr17:2664633 | G | C | 5 | a0001c0003t0010g0175 a0001c0003t0010g0176 a0001c0003t0010g0177 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-739G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664633 | |||||||
| chr17:2664665 | G | GCGCGCTC others(3): Show |
3 | a0001c0001t0003g0256 a0001c0001t0003g0263 a0001c0001t0003g0265 |
3 | HG01978.hp1 NA18968.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.33-706_33-705insGC others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(5): Show |
6 | a0001c0001t0003g0002 a0001c0001t0007g0196 a0001c0001t0007g0213 others(3): Show |
6 | HG01943.hp2 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-706_33-705insGC others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(7): Show |
14 | a0001c0001t0003g0099 a0001c0001t0003g0216 a0001c0001t0003g0255 others(11): Show |
14 | HG00558.hp2 HG02486.hp1 HG03130.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-706_33-705insGC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(9): Show |
5 | a0001c0001t0003g0254 a0001c0001t0003g0261 a0001c0001t0003g0262 others(2): Show |
5 | HG01346.hp1 NA18947.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-706_33-705insGC others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(11): Show |
1 | a0001c0001t0003g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(21): Show |
1 | a0001c0001t0003g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(26): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(29): Show |
1 | a0001c0001t0020g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(34): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(33): Show |
1 | a0001c0001t0003g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(38): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCGCTC others(35): Show |
2 | a0001c0001t0003g0222 a0001c0001t0003g0224 |
2 | NA18946.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.33-706_33-705insGC others(40): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCTCTC others(5): Show |
1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCGCTCTC others(31): Show |
1 | a0001c0001t0003g0219 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.33-706_33-705insGC others(36): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCT | 7 | a0001c0001t0001g0125 a0001c0001t0001g0174 a0001c0001t0002g0084 others(4): Show |
7 | HG02293.hp2 HG02683.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-680_33-679dupCT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(3): Show |
2 | a0001c0001t0001g0184 a0001c0001t0022g0183 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(7): Show |
2 | a0001c0001t0010g0181 a0001c0001t0021g0180 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(11): Show |
1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.33-704_33-703insGC others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(3): Show |
1 | a0001c0002t0006g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.33-704_33-703insGC others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(5): Show |
2 | a0001c0003t0010g0177 a0001c0003t0010g0178 |
2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(7): Show |
6 | a0001c0002t0006g0185 a0001c0002t0006g0187 a0001c0002t0006g0188 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-704_33-703insGC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(9): Show |
1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-704_33-703insGC others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCGCTC others(11): Show |
2 | a0001c0002t0006g0189 a0001c0003t0010g0176 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCT | 3 | a0001c0001t0001g0040 a0001c0001t0002g0158 a0001c0001t0017g0010 |
3 | HG03225.hp1 HG03654.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-682_33-679dupCT others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664665 | G | GCTCTCTC others(1): Show |
4 | a0001c0001t0001g0154 a0001c0001t0002g0118 a0001c0001t0003g0011 others(1): Show |
4 | HG00544.hp1 HG01515.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-686_33-679dupCT others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | ||||||
| chr17:2664680 | CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0011g0239 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.33-683_33-670delTC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664680 | ||||||
| chr17:2664684 | CTCTCTCT others(3): Show |
C | 20 | a0001c0001t0002g0234 a0001c0001t0004g0198 a0001c0001t0004g0199 others(17): Show |
20 | HG00438.hp2 HG01070.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.33-679_33-670delTT others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664684 | ||||||
| chr17:2664686 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0028g0018 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.33-686C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664686 | |||||||
| chr17:2664686 | CTCTCTCT others(1): Show |
C | 17 | a0001c0001t0004g0192 a0001c0001t0004g0229 a0001c0001t0004g0230 others(14): Show |
17 | HG00733.hp1 HG01168.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.33-678_33-671delTT others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664686 | ||||||
| chr17:2664688 | CTCTCTT | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(39): Show |
42 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.33-678_33-673delTT others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664688 | ||||||
| chr17:2664690 | CTCTT | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
13 | HG00099.hp1 HG01071.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-678_33-675delTT others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664690 | ||||||
| chr17:2664694 | T | C | 182 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0024 others(179): Show |
182 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.33-678T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664694 | |||||||
| chr17:2664734 | G | A | 6 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0016 others(3): Show |
6 | HG02622.hp2 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-638G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664734 | |||||||
| chr17:2664838 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(4): Show |
7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-534T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664838 | |||||||
| chr17:2664891 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.33-481A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664891 | |||||||
| chr17:2664981 | G | GTATA | 212 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.33-390_33-387dupTA others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664981 | ||||||
| chr17:2665012 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.33-360A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665012 | |||||||
| chr17:2665107 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.33-265T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665107 | |||||||
| chr17:2665190 | CAG | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-181_33-180delAG | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665190 | |||||||
| chr17:2665298 | T | C | 1 | a0001c0001t0015g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.33-74T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665298 | |||||||
| chr17:2665683 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG01071.hp1 HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117+227C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 3/10 | chr17 | 2665683 | |||||||
| chr17:2666002 | T | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118-14T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 3/10 | chr17 | 2666002 | |||||||
| chr17:2666133 | T | C | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+43T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666133 | |||||||
| chr17:2666139 | C | T | 2 | a0001c0001t0017g0010 a0001c0004t0036g0205 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192+49C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666139 | |||||||
| chr17:2666201 | T | C | 1 | a0001c0001t0011g0239 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.192+111T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666201 | |||||||
| chr17:2666264 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+174T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666264 | |||||||
| chr17:2666764 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.193-228G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666764 | |||||||
| chr17:2666902 | C | T | 1 | a0001c0001t0022g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193-90C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666902 | |||||||
| chr17:2667301 | TCCAGCCT others(1033): Show |
T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+107_399+1146de others(1): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 2667301 | ||||||
| chr17:2667757 | G | A | 272 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.399+559G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2667757 | |||||||
| chr17:2667965 | G | C | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.399+767G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2667965 | |||||||
| chr17:2667985 | G | C | 4 | a0001c0001t0002g0037 a0001c0001t0002g0056 a0001c0001t0002g0063 others(1): Show |
4 | HG00597.hp1 NA18944.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+787G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2667985 | |||||||
| chr17:2668114 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.399+916C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668114 | |||||||
| chr17:2668195 | G | A | 37 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(34): Show |
37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.399+997G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668195 | |||||||
| chr17:2668374 | A | G | 38 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(35): Show |
38 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.399+1176A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668374 | |||||||
| chr17:2668597 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.399+1399T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668597 | |||||||
| chr17:2668780 | C | T | 37 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(34): Show |
37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.400-1383C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668780 | |||||||
| chr17:2669064 | T | A | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.400-1099T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669064 | |||||||
| chr17:2669265 | A | AT | 38 | a0001c0001t0002g0234 a0001c0001t0003g0224 a0001c0001t0004g0192 others(35): Show |
38 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.400-882dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 2669265 | ||||||
| chr17:2669265 | A | ATT | 19 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(16): Show |
19 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.400-883_400-882dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 2669265 | ||||||
| chr17:2669452 | C | T | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.400-711C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669452 | |||||||
| chr17:2669478 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.400-685A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669478 | |||||||
| chr17:2669484 | G | T | 18 | a0001c0001t0003g0011 a0001c0001t0008g0137 a0001c0001t0008g0138 others(15): Show |
18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.400-679G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669484 | |||||||
| chr17:2669506 | G | A | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.400-657G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669506 | |||||||
| chr17:2669879 | A | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.400-284A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669879 | |||||||
| chr17:2670042 | T | G | 1 | a0001c0001t0005g0058 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.400-121T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2670042 | |||||||
| chr17:2670358 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.568+27C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670358 | |||||||
| chr17:2670564 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.568+233C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670564 | |||||||
| chr17:2670612 | T | G | 18 | a0001c0001t0001g0184 a0001c0001t0010g0181 a0001c0001t0021g0180 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.568+281T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670612 | |||||||
| chr17:2670818 | C | G | 1 | a0001c0003t0010g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.568+487C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670818 | |||||||
| chr17:2670892 | C | T | 17 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0140 others(14): Show |
17 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.568+561C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670892 | |||||||
| chr17:2671247 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.568+916C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671247 | |||||||
| chr17:2671365 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.568+1034C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671365 | |||||||
| chr17:2671369 | C | T | 1 | a0001c0001t0004g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568+1038C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671369 | |||||||
| chr17:2671497 | G | A | 1 | a0001c0001t0011g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.569-1158G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671497 | |||||||
| chr17:2671527 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
116 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.569-1128G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671527 | |||||||
| chr17:2671559 | T | C | 1 | a0001c0001t0005g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.569-1096T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671559 | |||||||
| chr17:2671568 | C | CT | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(44): Show |
47 | HG00438.hp2 HG00733.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.569-1087_569-1086i others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671568 | |||||||
| chr17:2671569 | A | AT | 5 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-1074dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2671569 | ||||||
| chr17:2671569 | A | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.569-1086A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671569 | |||||||
| chr17:2671596 | C | CT | 23 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0128 others(20): Show |
23 | HG01070.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.569-1038dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2671596 | ||||||
| chr17:2671596 | CT | C | 21 | a0001c0001t0002g0062 a0001c0001t0002g0163 a0001c0001t0003g0225 others(18): Show |
21 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.569-1038delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2671596 | ||||||
| chr17:2671651 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-1004G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671651 | |||||||
| chr17:2671675 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.569-980T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671675 | |||||||
| chr17:2671881 | G | T | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-774G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671881 | |||||||
| chr17:2671980 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-675C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671980 | |||||||
| chr17:2672049 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.569-606G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672049 | |||||||
| chr17:2672132 | T | G | 1 | a0001c0001t0009g0057 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.569-523T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672132 | |||||||
| chr17:2672197 | G | A | 1 | a0001c0001t0004g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.569-458G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672197 | |||||||
| chr17:2672285 | C | CA | 118 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.569-343dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | ||||||
| chr17:2672285 | C | CAA | 80 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0034 others(77): Show |
80 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.569-344_569-343dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | ||||||
| chr17:2672285 | C | CAAA | 21 | a0001c0001t0001g0064 a0001c0001t0001g0124 a0001c0001t0001g0134 others(18): Show |
21 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.569-345_569-343dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | ||||||
| chr17:2672285 | CA | C | 9 | a0001c0001t0003g0011 a0001c0001t0008g0143 a0001c0001t0021g0180 others(6): Show |
9 | HG01167.hp1 HG01515.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.569-343delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | ||||||
| chr17:2672285 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.569-353_569-343del others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | ||||||
| chr17:2672325 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0121 others(2): Show |
5 | HG00738.hp1 HG01099.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-330G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672325 | |||||||
| chr17:2673064 | G | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671+307G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673064 | |||||||
| chr17:2673068 | C | CA | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+320dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 2673068 | ||||||
| chr17:2673141 | C | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.671+384C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673141 | |||||||
| chr17:2673405 | A | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.671+648A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673405 | |||||||
| chr17:2673426 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.672-634T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673426 | |||||||
| chr17:2673442 | G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.672-618G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673442 | |||||||
| chr17:2673491 | T | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672-569T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673491 | |||||||
| chr17:2673502 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.672-558G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673502 | |||||||
| chr17:2673797 | C | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.672-263C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673797 | |||||||
| chr17:2673883 | A | T | 14 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0045 others(11): Show |
14 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.672-177A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673883 | |||||||
| chr17:2673936 | T | A | 1 | a0001c0001t0019g0268 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.672-124T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673936 | |||||||
| chr17:2674050 | A | C | 11 | a0001c0001t0010g0181 a0001c0001t0017g0010 a0001c0001t0021g0180 others(8): Show |
11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-10A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2674050 | |||||||
| chr17:2674556 | T | C | 2 | a0001c0001t0004g0249 a0001c0001t0004g0276 |
2 | HG01257.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.900+268T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674556 | |||||||
| chr17:2674686 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.900+398T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674686 | |||||||
| chr17:2674723 | T | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.900+435T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674723 | |||||||
| chr17:2674741 | C | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.900+453C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674741 | |||||||
| chr17:2674781 | C | G | 3 | a0001c0001t0010g0181 a0001c0001t0021g0180 a0001c0001t0022g0183 |
3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.900+493C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674781 | |||||||
| chr17:2675071 | G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.900+783G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675071 | |||||||
| chr17:2675080 | C | A | 38 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(35): Show |
38 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.900+792C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675080 | |||||||
| chr17:2675256 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.900+968G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675256 | |||||||
| chr17:2675354 | G | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.900+1066G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675354 | |||||||
| chr17:2675393 | C | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.900+1105C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675393 | |||||||
| chr17:2675634 | C | CT | 119 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(116): Show |
119 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.901-856dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 2675634 | ||||||
| chr17:2675634 | CT | C | 7 | a0001c0001t0001g0006 a0001c0001t0002g0149 a0001c0001t0003g0011 others(4): Show |
7 | HG01515.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.901-856delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 2675634 | ||||||
| chr17:2675662 | A | G | 1 | a0001c0001t0007g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.901-843A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675662 | |||||||
| chr17:2675675 | A | G | 1 | a0001c0001t0005g0167 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.901-830A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675675 | |||||||
| chr17:2675775 | A | G | 10 | a0001c0001t0001g0184 a0001c0001t0024g0193 a0001c0001t0029g0182 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.901-730A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675775 | |||||||
| chr17:2675782 | A | G | 1 | a0001c0001t0003g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.901-723A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675782 | |||||||
| chr17:2676106 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.901-399G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676106 | |||||||
| chr17:2676116 | G | A | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.901-389G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676116 | |||||||
| chr17:2676138 | C | G | 1 | a0001c0001t0002g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.901-367C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676138 | |||||||
| chr17:2676149 | C | T | 38 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(35): Show |
38 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.901-356C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676149 | |||||||
| chr17:2676159 | T | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.901-346T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676159 | |||||||
| chr17:2676249 | G | A | 6 | a0001c0001t0001g0195 a0001c0003t0010g0175 a0001c0003t0010g0176 others(3): Show |
6 | HG01099.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.901-256G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676249 | |||||||
| chr17:2676296 | T | G | 10 | a0001c0001t0003g0011 a0001c0001t0012g0012 a0001c0001t0012g0013 others(7): Show |
10 | HG01109.hp1 HG01515.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.901-209T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676296 | |||||||
| chr17:2676303 | G | A | 3 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0016 |
3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.901-202G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676303 | |||||||
| chr17:2676417 | A | AAT | 3 | a0001c0001t0010g0181 a0001c0001t0021g0180 a0001c0001t0022g0183 |
3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.901-81_901-80dupAT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 2676417 | ||||||
| chr17:2676426 | C | G | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.901-79C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676426 | |||||||
| chr17:2676706 | G | A | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1002+100G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2676706 | |||||||
| chr17:2676889 | G | A | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1002+283G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2676889 | |||||||
| chr17:2676971 | G | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1002+365G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2676971 | |||||||
| chr17:2677077 | C | T | 8 | a0001c0001t0024g0193 a0001c0002t0006g0185 a0001c0002t0006g0186 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1002+471C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677077 | |||||||
| chr17:2677358 | A | G | 1 | a0001c0001t0011g0241 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1002+752A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677358 | |||||||
| chr17:2677415 | G | T | 2 | a0001c0001t0013g0218 a0001c0001t0013g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1002+809G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677415 | |||||||
| chr17:2677502 | T | A | 1 | a0001c0001t0004g0250 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1002+896T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677502 | |||||||
| chr17:2677523 | C | T | 1 | a0001c0001t0019g0268 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1002+917C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677523 | |||||||
| chr17:2677527 | CAT | C | 35 | a0001c0001t0003g0002 a0001c0001t0003g0099 a0001c0001t0003g0216 others(32): Show |
35 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.1002+924_1002+925d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2677527 | ||||||
| chr17:2677778 | C | T | 1 | a0001c0001t0012g0279 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1002+1172C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677778 | |||||||
| chr17:2677785 | C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1002+1179C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677785 | |||||||
| chr17:2677801 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1002+1195C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677801 | |||||||
| chr17:2677827 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1002+1221C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677827 | |||||||
| chr17:2677856 | A | AAAAT | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1002+1270_1002+127 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2677856 | ||||||
| chr17:2677856 | A | AAAATAAA others(1): Show |
3 | a0001c0001t0008g0137 a0001c0001t0008g0140 a0001c0001t0008g0142 |
3 | HG02451.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1002+1266_1002+127 others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2677856 | ||||||
| chr17:2677899 | C | G | 1 | a0001c0001t0002g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1002+1293C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677899 | |||||||
| chr17:2677966 | A | G | 12 | a0001c0001t0001g0079 a0001c0001t0001g0161 a0001c0001t0002g0038 others(9): Show |
12 | HG00323.hp2 HG00438.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002+1360A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677966 | |||||||
| chr17:2678114 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+1508G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678114 | |||||||
| chr17:2678237 | G | A | 218 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1002+1631G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678237 | |||||||
| chr17:2678383 | CAA | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+1778_1002+177 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678383 | |||||||
| chr17:2678400 | C | CA | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
63 | HG00438.hp2 HG00544.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1003-1745dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | ||||||
| chr17:2678400 | C | CAA | 15 | a0001c0001t0002g0115 a0001c0001t0004g0192 a0001c0001t0004g0201 others(12): Show |
15 | HG00544.hp2 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1003-1746_1003-174 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | ||||||
| chr17:2678400 | CA | C | 10 | a0001c0001t0001g0184 a0001c0001t0002g0054 a0001c0001t0024g0193 others(7): Show |
10 | HG01891.hp1 HG02015.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1003-1745delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | ||||||
| chr17:2678400 | CAAAAAAA | C | 26 | a0001c0001t0001g0105 a0001c0001t0005g0004 a0001c0001t0005g0050 others(23): Show |
26 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1003-1751_1003-174 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | ||||||
| chr17:2678434 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0029g0182 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1003-1730C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678434 | |||||||
| chr17:2678514 | C | T | 1 | a0001c0001t0041g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1003-1650C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678514 | |||||||
| chr17:2678579 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003-1585G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678579 | |||||||
| chr17:2679015 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1003-1149T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679015 | |||||||
| chr17:2679045 | CGTACATG others(4): Show |
C | 1 | a0001c0001t0002g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1003-1115_1003-110 others(15): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679045 | ||||||
| chr17:2679152 | G | A | 5 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0235 others(2): Show |
5 | HG01255.hp2 HG01257.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-1012G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679152 | |||||||
| chr17:2679198 | C | A | 6 | a0001c0001t0012g0013 a0001c0001t0012g0014 a0001c0001t0012g0016 others(3): Show |
6 | HG02622.hp2 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-966C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679198 | |||||||
| chr17:2679361 | GATGATTA others(9): Show |
G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1003-796_1003-781d others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679361 | ||||||
| chr17:2679458 | TTGGATGG others(17): Show |
T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1003-639_1003-616d others(26): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679458 | ||||||
| chr17:2679478 | TTGGATGG others(25): Show |
T | 1 | a0001c0001t0002g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1003-671_1003-640d others(34): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679478 | ||||||
| chr17:2679502 | TTGGATGG others(25): Show |
T | 2 | a0001c0001t0017g0010 a0001c0004t0036g0205 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1003-643_1003-612d others(34): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679502 | ||||||
| chr17:2679506 | ATGGATGG others(13): Show |
A | 10 | a0001c0001t0003g0011 a0001c0001t0003g0225 a0001c0001t0003g0227 others(7): Show |
10 | HG01515.hp2 HG02622.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-639_1003-620d others(22): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679506 | ||||||
| chr17:2679514 | ATGGATGG others(5): Show |
A | 2 | a0001c0001t0001g0019 a0001c0001t0028g0018 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-639_1003-628d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679514 | ||||||
| chr17:2679540 | G | C | 1 | a0001c0001t0015g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1003-624G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679540 | |||||||
| chr17:2679541 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0028g0018 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-623G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679541 | |||||||
| chr17:2679542 | A | T | 2 | a0001c0001t0001g0019 a0001c0001t0028g0018 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-622A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679542 | |||||||
| chr17:2679544 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0028g0018 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-620G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679544 | |||||||
| chr17:2679584 | GGATA | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0028g0018 |
3 | HG02559.hp2 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-572_1003-569d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679584 | ||||||
| chr17:2679610 | A | G | 36 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(33): Show |
36 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1003-554A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679610 | |||||||
| chr17:2679614 | ATGGATGA others(1): Show |
A | 24 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0064 others(21): Show |
24 | HG01071.hp1 HG01074.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1003-535_1003-528d others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679614 | ||||||
| chr17:2679618 | ATGAT | A | 36 | a0001c0001t0002g0234 a0001c0001t0004g0192 a0001c0001t0004g0198 others(33): Show |
36 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1003-543_1003-540d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679618 | ||||||
| chr17:2679622 | TTGGATGA others(5): Show |
T | 6 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0003g0224 others(3): Show |
6 | NA18946.hp1 NA18979.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-535_1003-524d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679622 | ||||||
| chr17:2679622 | TTGGATGA others(9): Show |
T | 1 | a0001c0001t0008g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1003-535_1003-520d others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679622 | ||||||
| chr17:2679626 | ATGAT | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1003-535_1003-532d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679626 | ||||||
| chr17:2679627 | T | TG | 6 | a0001c0001t0002g0043 a0001c0001t0002g0084 a0001c0001t0012g0012 others(3): Show |
6 | HG02738.hp2 HG02965.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-536dupG | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679627 | ||||||
| chr17:2679629 | A | G | 52 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0066 others(49): Show |
52 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1003-535A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679629 | |||||||
| chr17:2679630 | T | A | 52 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0066 others(49): Show |
52 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1003-534T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679630 | |||||||
| chr17:2679630 | T | TGGA | 6 | a0001c0001t0002g0043 a0001c0001t0002g0084 a0001c0001t0012g0012 others(3): Show |
6 | HG02738.hp2 HG02965.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-534_1003-533i others(5): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679630 | |||||||
| chr17:2679630 | TTGGA | T | 2 | a0001c0001t0004g0249 a0001c0001t0004g0276 |
2 | HG01257.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1003-496_1003-493d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679630 | ||||||
| chr17:2679814 | C | A | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1003-350C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679814 | |||||||
| chr17:2679896 | T | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1003-268T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679896 | |||||||
| chr17:2679930 | T | C | 2 | a0001c0001t0003g0225 a0001c0001t0003g0227 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1003-234T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679930 | |||||||
| chr17:2679980 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1003-184G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679980 | |||||||
| chr17:2679984 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0028g0018 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-180G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679984 | |||||||
| chr17:2680682 | G | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1159+362G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2680682 | |||||||
| chr17:2680684 | T | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1159+364T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2680684 | |||||||
| chr17:2680817 | C | G | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1159+497C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2680817 | |||||||
| chr17:2681370 | T | A | 44 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0079 others(41): Show |
44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1160-359T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681370 | |||||||
| chr17:2681452 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1160-277G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681452 | |||||||
| chr17:2681540 | G | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-189G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681540 | |||||||
| chr17:2681596 | G | T | 8 | a0001c0001t0012g0012 a0001c0001t0012g0013 a0001c0001t0012g0014 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-133G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681596 | |||||||
| chr17:2681601 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1160-128A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681601 | |||||||
| chr17:2681652 | G | A | 44 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0079 others(41): Show |
44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1160-77G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681652 |