Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80227 |
| ensemblid | ENSG00000175575.13 |
| hgncid | 25687 |
| symbol | PAAF1 |
| name | proteasomal ATPase associated factor 1 |
| refseq_nuc | NM_025155.3 |
| refseq_prot | NP_079431.1 |
| ensembl_nuc | ENST00000310571.8 |
| ensembl_prot | ENSP00000311665.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 73876999 |
| end | 73931114 |
| strand | + |
| ver | v1.2 |
| region | chr11:73876999-73931114 |
| region5000 | chr11:73871999-73936114 |
| regionname0 | PAAF1_chr11_73876999_73931114 |
| regionname5000 | PAAF1_chr11_73871999_73936114 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 392 | 262 | 78 | 46 | 99 | 7 | 30 | 83 | PAAF1_chr11_73871999_73936114 | PAAF1 | MAAPL others(387): Show |
chr11 | 73871999 | 73936114 |
| a0002 | 0/0 | 392 | 55 | 13 | 6 | 31 | 0 | 5 | 25 | PAAF1_chr11_73871999_73936114 | PAAF1 | MAAPL others(387): Show |
chr11 | 73871999 | 73936114 |
| a0003 | 0/0 | 392 | 50 | 3 | 5 | 28 | 3 | 11 | 20 | PAAF1_chr11_73871999_73936114 | PAAF1 | MAAPL others(387): Show |
chr11 | 73871999 | 73936114 |
| a0004 | 0/0 | 392 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | MAAPL others(387): Show |
chr11 | 73871999 | 73936114 |
| a0005 | 0/0 | 392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | MAAPL others(387): Show |
chr11 | 73871999 | 73936114 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1176 | 258 | 77 | 46 | 96 | 7 | 30 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 | ||
| a0001c0004 | 0/0 | 1176 | 3 | 0 | 0 | 3 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 | ||
| a0001c0008 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 | ||
| a0002c0002 | 0/0 | 1176 | 55 | 13 | 6 | 31 | 0 | 5 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 | ||
| a0003c0003 | 0/0 | 1176 | 48 | 3 | 5 | 26 | 3 | 11 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 | ||
| a0003c0006 | 0/0 | 1176 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 | ||
| a0004c0005 | 0/0 | 1176 | 2 | 1 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 | ||
| a0005c0007 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | ATGGC others(1171): Show |
chr11 | 73871999 | 73936114 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4954 | 106 | 4 | 23 | 56 | 3 | 18 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0002 | 0/0 | 4954 | 2 | 1 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0003 | 0/0 | 4954 | 40 | 9 | 8 | 18 | 1 | 4 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0004 | 0/0 | 4954 | 24 | 9 | 7 | 3 | 3 | 2 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0005 | 0/0 | 4954 | 12 | 12 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0006 | 0/0 | 4953 | 10 | 5 | 3 | 0 | 0 | 2 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0007 | 0/0 | 4954 | 9 | 9 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0008 | 0/0 | 4953 | 8 | 8 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0009 | 0/0 | 4954 | 7 | 0 | 0 | 7 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0011 | 0/0 | 4953 | 3 | 3 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0012 | 0/0 | 4954 | 3 | 3 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0013 | 0/0 | 4955 | 3 | 2 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4950): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0014 | 0/0 | 4952 | 3 | 3 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4947): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0015 | 0/0 | 4954 | 2 | 2 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0016 | 0/0 | 4953 | 2 | 0 | 0 | 0 | 0 | 2 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0017 | 0/0 | 4954 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0020 | 0/0 | 4954 | 2 | 0 | 1 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0021 | 0/0 | 4954 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0022 | 0/0 | 4952 | 2 | 2 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4947): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0023 | 0/0 | 4955 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4950): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0024 | 0/0 | 4954 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0025 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0027 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0030 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0033 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4950): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0034 | 0/0 | 4954 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0035 | 0/0 | 4942 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4937): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0036 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0037 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0038 | 0/0 | 4955 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4950): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0040 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0041 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0042 | 0/0 | 4954 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0043 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0001t0044 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4964): Show |
chr11 | 73871999 | 73936114 |
| a0001c0004t0001 | 0/0 | 4954 | 3 | 0 | 0 | 3 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0001c0008t0039 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0002c0002t0002 | 0/0 | 4954 | 50 | 13 | 6 | 26 | 0 | 5 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0002c0002t0010 | 0/0 | 4954 | 4 | 0 | 0 | 4 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0002c0002t0028 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0003c0003t0002 | 0/0 | 4954 | 42 | 2 | 5 | 23 | 3 | 9 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0003c0003t0018 | 0/0 | 4954 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0003c0003t0026 | 0/0 | 4954 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0003c0003t0029 | 0/0 | 4954 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0003c0003t0031 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4948): Show |
chr11 | 73871999 | 73936114 |
| a0003c0003t0032 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0003c0006t0002 | 0/0 | 4954 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0004c0005t0019 | 0/0 | 4954 | 2 | 1 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| a0005c0007t0002 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | GGGCT others(4949): Show |
chr11 | 73871999 | 73936114 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0005 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0008g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0009g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0009g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0013g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0013g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0014g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0015g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0016g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0016g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0017g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0017g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0020g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0020g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0021g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0021g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0022g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0022g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0023g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0024g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0025g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0027g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0030g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0033g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0034g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0035g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0036g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0037g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0038g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0040g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0041g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0042g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0043g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0001t0044g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0001c0008t0039g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0010g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0002c0002t0028g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0018g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0018g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0026g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0029g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0031g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0003t0032g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0006t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0003c0006t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0004c0005t0019g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0004c0005t0019g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| a0005c0007t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0239 | EUR | FIN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00408 | hp1 | a0003 | c0003 | t0018 | g0277 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0278 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00558 | hp2 | a0003 | c0006 | t0002 | g0297 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00621 | hp2 | a0003 | c0003 | t0002 | g0292 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0269 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0209 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00673 | hp1 | a0003 | c0003 | t0002 | g0282 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0332 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0327 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01074 | hp1 | a0004 | c0005 | t0019 | g0076 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0257 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01168 | hp1 | a0003 | c0003 | t0002 | g0288 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0089 | AMR | PUR | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0016 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0329 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01256 | hp2 | a0001 | c0001 | t0042 | g0249 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0337 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0308 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01496 | hp2 | a0001 | c0001 | t0020 | g0206 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0101 | EUR | IBS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0097 | EUR | IBS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0016 | EUR | IBS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01517 | hp1 | a0003 | c0003 | t0002 | g0210 | EUR | IBS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0078 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0011 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0304 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01975 | hp2 | a0001 | c0001 | t0024 | g0215 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0081 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02056 | hp1 | a0001 | c0001 | t0023 | g0118 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0023 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | KHV | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02155 | hp1 | a0003 | c0003 | t0018 | g0020 | EAS | CDX | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0180 | EAS | CDX | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02165 | hp2 | a0001 | c0001 | t0043 | g0255 | EAS | CDX | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02257 | hp2 | a0003 | c0003 | t0002 | g0300 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0083 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0266 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02451 | hp2 | a0001 | c0001 | t0022 | g0261 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0079 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02602 | hp2 | a0003 | c0003 | t0002 | g0276 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0310 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02615 | hp2 | a0001 | c0001 | t0030 | g0028 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02630 | hp1 | a0003 | c0003 | t0002 | g0301 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0311 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0314 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02683 | hp2 | a0003 | c0003 | t0029 | g0275 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0287 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0331 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0330 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0315 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0260 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0259 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02886 | hp2 | a0001 | c0001 | t0025 | g0256 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0323 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02896 | hp1 | a0005 | c0007 | t0002 | g0047 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0326 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02970 | hp1 | a0001 | c0001 | t0014 | g0011 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0321 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0059 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0324 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0085 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0082 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03209 | hp2 | a0001 | c0001 | t0022 | g0262 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0317 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03225 | hp2 | a0003 | c0003 | t0032 | g0302 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0322 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0325 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03490 | hp2 | a0003 | c0003 | t0002 | g0290 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03491 | hp1 | a0003 | c0003 | t0002 | g0298 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03491 | hp2 | a0001 | c0001 | t0016 | g0333 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0022 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03492 | hp2 | a0001 | c0001 | t0016 | g0328 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0313 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0312 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0307 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03688 | hp1 | a0001 | c0001 | t0020 | g0185 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03710 | hp2 | a0003 | c0003 | t0002 | g0274 | SAS | PJL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03834 | hp1 | a0001 | c0001 | t0034 | g0197 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0022 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0271 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0057 | SAS | BEB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04199 | hp2 | a0003 | c0003 | t0026 | g0283 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0117 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | YRI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0293 | EAS | CHB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18612 | hp2 | a0001 | c0001 | t0038 | g0125 | EAS | CHB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | YRI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | YRI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18939 | hp1 | a0002 | c0002 | t0010 | g0052 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18942 | hp2 | a0002 | c0002 | t0010 | g0053 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18945 | hp2 | a0003 | c0003 | t0002 | g0273 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18948 | hp1 | a0001 | c0001 | t0009 | g0105 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18949 | hp1 | a0003 | c0003 | t0002 | g0272 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0291 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18953 | hp2 | a0001 | c0001 | t0009 | g0092 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0091 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18963 | hp1 | a0001 | c0001 | t0009 | g0108 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18963 | hp2 | a0001 | c0001 | t0021 | g0229 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18966 | hp1 | a0003 | c0006 | t0002 | g0020 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18969 | hp1 | a0001 | c0001 | t0035 | g0005 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18972 | hp1 | a0003 | c0003 | t0002 | g0270 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18972 | hp2 | a0001 | c0001 | t0036 | g0171 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18978 | hp1 | a0003 | c0003 | t0002 | g0265 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18982 | hp2 | a0001 | c0001 | t0021 | g0240 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18985 | hp1 | a0001 | c0001 | t0044 | g0241 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18988 | hp1 | a0003 | c0003 | t0002 | g0294 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18991 | hp2 | a0001 | c0004 | t0001 | g0193 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18993 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18995 | hp2 | a0002 | c0002 | t0028 | g0048 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0104 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19001 | hp2 | a0003 | c0003 | t0031 | g0284 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19004 | hp1 | a0002 | c0002 | t0010 | g0054 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0175 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19030 | hp1 | a0001 | c0008 | t0039 | g0263 | AFR | LWK | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19030 | hp2 | a0001 | c0001 | t0027 | g0026 | AFR | LWK | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0320 | AFR | LWK | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | LWK | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0295 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19057 | hp2 | a0001 | c0001 | t0017 | g0107 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19059 | hp1 | a0001 | c0001 | t0037 | g0119 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19059 | hp2 | a0001 | c0001 | t0041 | g0219 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19067 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0088 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19070 | hp1 | a0001 | c0001 | t0009 | g0094 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0296 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19075 | hp1 | a0003 | c0003 | t0002 | g0279 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19075 | hp2 | a0001 | c0001 | t0017 | g0087 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19076 | hp2 | a0003 | c0003 | t0002 | g0309 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19077 | hp2 | a0003 | c0003 | t0002 | g0289 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19082 | hp2 | a0003 | c0003 | t0002 | g0280 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19087 | hp2 | a0002 | c0002 | t0010 | g0055 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19091 | hp1 | a0003 | c0003 | t0002 | g0023 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19240 | hp1 | a0004 | c0005 | t0019 | g0069 | AFR | YRI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | YRI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ASW | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0318 | AFR | ASW | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0096 | EUR | TSI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20805 | hp2 | a0003 | c0003 | t0002 | g0285 | EUR | TSI | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20905 | hp1 | a0003 | c0003 | t0002 | g0286 | SAS | GIH | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | GIH | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | CLM | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0040 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0319 | AFR | ACB | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03471 | hp1 | a0001 | c0001 | t0033 | g0258 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | MSL | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | USA | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0070 | AFR | USA | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0316 | AFR | USA | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | USA | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0077 | AFR | LWK | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| NA21309 | hp2 | a0001 | c0001 | t0040 | g0299 | AFR | LWK | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0139 | REF | REF | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | PAAF1_chr11_73871999_73936114 | PAAF1 | chr11 | 73871999 | 73936114 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73900304 | G | C | 1 | a0003 | 50 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(47): Show |
missense_variant | MODERATE | c.416G>C | p.Cys139Ser | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/12 | 439/4954 | 416/1179 | 139/392 | chr11 | 73900304 | |||
| chr11:73909492 | C | G | 3 | a0002 a0004 a0005 |
58 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(55): Show |
missense_variant | MODERATE | c.626C>G | p.Ala209Gly | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/12 | 649/4954 | 626/1179 | 209/392 | chr11 | 73909492 | |||
| chr11:73909519 | G | A | 1 | a0004 | 2 | HG01074.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.653G>A | p.Gly218Asp | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/12 | 676/4954 | 653/1179 | 218/392 | chr11 | 73909519 | |||
| chr11:73918955 | C | T | 1 | a0005 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.941C>T | p.Pro314Leu | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/12 | 964/4954 | 941/1179 | 314/392 | chr11 | 73918955 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73899205 | G | T | 2 | a0001c0008 a0003c0006 |
3 | HG00558.hp2 NA18966.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.342G>T | p.Gly114Gly | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/12 | 365/4954 | 342/1179 | 114/392 | chr11 | 73899205 | |||
| chr11:73909508 | T | C | 1 | a0001c0004 | 3 | HG02155.hp2 NA18991.hp2 NA19009.hp1 |
synonymous_variant | LOW | c.642T>C | p.Leu214Leu | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/12 | 665/4954 | 642/1179 | 214/392 | chr11 | 73909508 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73927680 | AG | A | 2 | a0001c0001t0014 a0001c0001t0022 |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*319delG | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 319 | chr11 | 73927680 | ||||||
| chr11:73927790 | T | C | 1 | a0001c0001t0015 | 2 | HG02055.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*428T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 428 | chr11 | 73927790 | ||||||
| chr11:73927813 | C | T | 6 | a0001c0001t0003 a0001c0001t0021 a0001c0001t0041 others(3): Show |
46 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 451 | chr11 | 73927813 | ||||||
| chr11:73927839 | G | C | 1 | a0002c0002t0010 | 4 | NA18939.hp1 NA18942.hp2 NA19004.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*477G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 477 | chr11 | 73927839 | ||||||
| chr11:73927860 | T | A | 1 | a0001c0001t0023 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 498 | chr11 | 73927860 | ||||||
| chr11:73927988 | C | T | 2 | a0001c0001t0014 a0001c0001t0022 |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*626C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 626 | chr11 | 73927988 | ||||||
| chr11:73928071 | A | C | 1 | a0001c0001t0044 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 709 | chr11 | 73928071 | ||||||
| chr11:73928145 | G | T | 1 | a0001c0001t0040 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*783G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 783 | chr11 | 73928145 | ||||||
| chr11:73928395 | T | G | 1 | a0001c0001t0024 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1033T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1033 | chr11 | 73928395 | ||||||
| chr11:73928439 | C | T | 1 | a0001c0008t0039 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1077 | chr11 | 73928439 | ||||||
| chr11:73928521 | TC | T | 5 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0011 others(2): Show |
24 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1161delC | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1161 | INFO_REALIGN_3_PRIME | chr11 | 73928521 | |||||
| chr11:73928528 | C | CAGTACAT others(8): Show |
1 | a0001c0001t0044 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1167_*1181dupAGTA others(11): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1182 | INFO_REALIGN_3_PRIME | chr11 | 73928528 | |||||
| chr11:73928666 | T | C | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
240 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1304T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1304 | chr11 | 73928666 | ||||||
| chr11:73928667 | T | A | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
240 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1305T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1305 | chr11 | 73928667 | ||||||
| chr11:73928721 | G | A | 1 | a0001c0001t0025 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1359G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1359 | chr11 | 73928721 | ||||||
| chr11:73928748 | C | T | 1 | a0004c0005t0019 | 2 | HG01074.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1386C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1386 | chr11 | 73928748 | ||||||
| chr11:73928783 | T | C | 1 | a0001c0001t0021 | 2 | NA18963.hp2 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1421T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1421 | chr11 | 73928783 | ||||||
| chr11:73928869 | C | G | 1 | a0001c0001t0009 | 7 | NA18948.hp1 NA18953.hp2 NA18961.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1507C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1507 | chr11 | 73928869 | ||||||
| chr11:73929032 | T | C | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0014 others(2): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1670T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1670 | chr11 | 73929032 | ||||||
| chr11:73929041 | G | A | 1 | a0003c0003t0026 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1679G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1679 | chr11 | 73929041 | ||||||
| chr11:73929055 | A | AT | 4 | a0001c0001t0013 a0001c0001t0023 a0001c0001t0033 others(1): Show |
6 | HG01106.hp1 HG02056.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1705dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1706 | INFO_REALIGN_3_PRIME | chr11 | 73929055 | |||||
| chr11:73929055 | AT | A | 8 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0014 others(5): Show |
41 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1705delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1705 | INFO_REALIGN_3_PRIME | chr11 | 73929055 | |||||
| chr11:73929105 | C | T | 3 | a0001c0001t0007 a0001c0001t0012 a0001c0008t0039 |
13 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1743C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1743 | chr11 | 73929105 | ||||||
| chr11:73929119 | C | T | 1 | a0001c0001t0020 | 2 | HG01496.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1757C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1757 | chr11 | 73929119 | ||||||
| chr11:73929350 | G | A | 1 | a0001c0001t0042 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1988G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 1988 | chr11 | 73929350 | ||||||
| chr11:73929544 | A | G | 2 | a0001c0001t0007 a0001c0001t0012 |
12 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2182A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2182 | chr11 | 73929544 | ||||||
| chr11:73929744 | T | G | 1 | a0001c0001t0034 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2382T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2382 | chr11 | 73929744 | ||||||
| chr11:73929795 | G | A | 1 | a0001c0001t0012 | 3 | HG01884.hp1 HG02486.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2433G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2433 | chr11 | 73929795 | ||||||
| chr11:73929848 | G | A | 1 | a0001c0001t0033 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2486G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2486 | chr11 | 73929848 | ||||||
| chr11:73929854 | C | T | 2 | a0001c0001t0013 a0001c0001t0033 |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2492C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2492 | chr11 | 73929854 | ||||||
| chr11:73929886 | G | A | 2 | a0001c0001t0014 a0001c0001t0022 |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2524G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2524 | chr11 | 73929886 | ||||||
| chr11:73929980 | C | T | 1 | a0003c0003t0032 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2618C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2618 | chr11 | 73929980 | ||||||
| chr11:73930013 | G | A | 1 | a0001c0001t0042 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2651G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2651 | chr11 | 73930013 | ||||||
| chr11:73930021 | G | A | 2 | a0001c0001t0008 a0001c0001t0011 |
11 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2659G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2659 | chr11 | 73930021 | ||||||
| chr11:73930108 | C | G | 2 | a0001c0001t0013 a0001c0001t0033 |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2746C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2746 | chr11 | 73930108 | ||||||
| chr11:73930146 | G | A | 1 | a0001c0001t0017 | 2 | NA19057.hp2 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2784G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2784 | chr11 | 73930146 | ||||||
| chr11:73930198 | G | GTC | 3 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2838_*2839dupCT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2840 | INFO_REALIGN_3_PRIME | chr11 | 73930198 | |||||
| chr11:73930268 | G | A | 1 | a0003c0003t0018 | 2 | HG00408.hp1 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2906G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2906 | chr11 | 73930268 | ||||||
| chr11:73930355 | G | A | 1 | a0001c0001t0027 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2993G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 2993 | chr11 | 73930355 | ||||||
| chr11:73930372 | GA | G | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(2): Show |
35 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3021delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3021 | INFO_REALIGN_3_PRIME | chr11 | 73930372 | |||||
| chr11:73930473 | G | A | 1 | a0002c0002t0028 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3111G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3111 | chr11 | 73930473 | ||||||
| chr11:73930526 | C | T | 1 | a0001c0001t0011 | 3 | HG02630.hp2 HG02647.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3164C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3164 | chr11 | 73930526 | ||||||
| chr11:73930543 | T | A | 3 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3181T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3181 | chr11 | 73930543 | ||||||
| chr11:73930566 | A | C | 1 | a0001c0001t0043 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3204A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3204 | chr11 | 73930566 | ||||||
| chr11:73930607 | T | C | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0014 others(2): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3245T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3245 | chr11 | 73930607 | ||||||
| chr11:73930645 | A | G | 39 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(36): Show |
252 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*3283A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3283 | chr11 | 73930645 | ||||||
| chr11:73930698 | G | A | 1 | a0001c0001t0014 | 3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3336G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3336 | chr11 | 73930698 | ||||||
| chr11:73930713 | C | G | 1 | a0001c0001t0016 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3351C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3351 | chr11 | 73930713 | ||||||
| chr11:73930734 | G | A | 2 | a0001c0001t0040 a0001c0008t0039 |
2 | NA19030.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3372G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3372 | chr11 | 73930734 | ||||||
| chr11:73930743 | T | C | 1 | a0003c0003t0029 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3381T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3381 | chr11 | 73930743 | ||||||
| chr11:73930762 | A | T | 1 | a0001c0001t0030 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3400A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3400 | chr11 | 73930762 | ||||||
| chr11:73930762 | AATATGTA others(5): Show |
A | 1 | a0001c0001t0035 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3417_*3428delGTAT others(8): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3417 | INFO_REALIGN_3_PRIME | chr11 | 73930762 | |||||
| chr11:73930763 | AT | A | 3 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 |
32 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3402delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3402 | chr11 | 73930763 | ||||||
| chr11:73930837 | C | T | 1 | a0001c0001t0036 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3475C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3475 | chr11 | 73930837 | ||||||
| chr11:73931002 | G | T | 1 | a0001c0008t0039 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3640G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 12/12 | 3640 | chr11 | 73931002 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73877077 | A | C | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.47+9A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877077 | |||||||
| chr11:73877195 | G | A | 69 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0007g0009 others(66): Show |
76 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.47+127G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877195 | |||||||
| chr11:73877340 | A | C | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | NA18944.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.47+272A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877340 | |||||||
| chr11:73877406 | T | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.47+338T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877406 | |||||||
| chr11:73877482 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.47+414C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877482 | |||||||
| chr11:73877525 | A | G | 186 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(183): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.47+457A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877525 | |||||||
| chr11:73877606 | C | A | 2 | a0002c0002t0002g0024 a0002c0002t0002g0025 |
2 | HG00597.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.47+538C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877606 | |||||||
| chr11:73877612 | G | A | 24 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(21): Show |
25 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.47+544G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877612 | |||||||
| chr11:73877763 | A | G | 1 | a0001c0001t0043g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.47+695A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877763 | |||||||
| chr11:73877768 | C | A | 1 | a0001c0001t0025g0256 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.47+700C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877768 | |||||||
| chr11:73877835 | G | A | 3 | a0001c0001t0002g0027 a0001c0001t0027g0026 a0001c0001t0030g0028 |
3 | HG02615.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.47+767G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73877835 | |||||||
| chr11:73878094 | G | A | 5 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0031 others(2): Show |
5 | NA18977.hp2 NA18983.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.48-685G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878094 | |||||||
| chr11:73878139 | G | T | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.48-640G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878139 | |||||||
| chr11:73878219 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.48-560A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878219 | |||||||
| chr11:73878257 | G | A | 6 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(3): Show |
7 | HG02717.hp1 HG02965.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.48-522G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878257 | |||||||
| chr11:73878327 | T | C | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG02056.hp1 HG04184.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.48-452T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878327 | |||||||
| chr11:73878685 | G | A | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.48-94G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878685 | |||||||
| chr11:73878709 | C | T | 1 | a0003c0003t0002g0309 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.48-70C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878709 | |||||||
| chr11:73878710 | T | C | 1 | a0003c0003t0002g0309 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.48-69T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878710 | |||||||
| chr11:73878712 | C | T | 1 | a0003c0003t0002g0309 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.48-67C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 1/11 | chr11 | 73878712 | |||||||
| chr11:73878857 | G | A | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.88+38G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73878857 | |||||||
| chr11:73879107 | A | T | 3 | a0002c0002t0002g0306 a0002c0002t0002g0307 a0002c0002t0002g0308 |
3 | HG01496.hp1 HG02148.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.88+288A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879107 | |||||||
| chr11:73879119 | C | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+300C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879119 | |||||||
| chr11:73879209 | T | G | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.88+390T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879209 | |||||||
| chr11:73879216 | C | G | 1 | a0002c0002t0002g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.88+397C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879216 | |||||||
| chr11:73879265 | A | G | 226 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(223): Show |
245 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.88+446A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879265 | |||||||
| chr11:73879401 | A | G | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.88+582A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879401 | |||||||
| chr11:73879458 | C | T | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+639C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879458 | |||||||
| chr11:73879608 | G | A | 40 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0018 others(37): Show |
46 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.88+789G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879608 | |||||||
| chr11:73879689 | G | A | 40 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0018 others(37): Show |
46 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.88+870G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879689 | |||||||
| chr11:73879696 | T | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+877T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879696 | |||||||
| chr11:73879715 | C | CA | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+904dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73879715 | ||||||
| chr11:73879768 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.88+949G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879768 | |||||||
| chr11:73879777 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.88+958A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879777 | |||||||
| chr11:73879873 | T | TA | 33 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(30): Show |
34 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.88+1065dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73879873 | ||||||
| chr11:73879922 | T | C | 1 | a0001c0001t0023g0118 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.88+1103T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879922 | |||||||
| chr11:73879960 | C | G | 4 | a0001c0001t0003g0250 a0001c0001t0003g0251 a0001c0001t0003g0252 others(1): Show |
4 | HG01099.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1141C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73879960 | |||||||
| chr11:73880224 | C | T | 1 | a0002c0002t0002g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.88+1405C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880224 | |||||||
| chr11:73880295 | A | AAT | 3 | a0001c0001t0004g0116 a0001c0001t0022g0261 a0001c0001t0022g0262 |
3 | HG02451.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.88+1488_88+1489dup others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880295 | ||||||
| chr11:73880481 | T | C | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+1662T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880481 | |||||||
| chr11:73880482 | T | TA | 8 | a0001c0001t0001g0131 a0001c0001t0001g0264 a0001c0001t0002g0337 others(5): Show |
8 | HG01358.hp1 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+1679dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880482 | ||||||
| chr11:73880482 | TA | T | 35 | a0001c0001t0003g0248 a0001c0001t0004g0012 a0001c0001t0004g0090 others(32): Show |
36 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.88+1679delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880482 | ||||||
| chr11:73880519 | T | TA | 5 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(2): Show |
6 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+1709dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880519 | ||||||
| chr11:73880558 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+1739G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880558 | |||||||
| chr11:73880559 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0211 a0001c0001t0001g0212 others(5): Show |
9 | HG00733.hp2 HG01081.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.88+1740C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880559 | |||||||
| chr11:73880611 | C | T | 3 | a0003c0003t0002g0016 a0003c0003t0002g0209 a0003c0003t0002g0210 |
4 | HG00642.hp2 HG01255.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1792C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880611 | |||||||
| chr11:73880649 | C | G | 25 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(22): Show |
26 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+1830C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880649 | |||||||
| chr11:73880649 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+1830C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880649 | |||||||
| chr11:73880686 | C | CG | 6 | a0001c0001t0001g0334 a0001c0001t0005g0305 a0001c0001t0006g0330 others(3): Show |
6 | HG00735.hp1 HG01070.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+1868dupG | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880686 | ||||||
| chr11:73880687 | G | GA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(59): Show |
69 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.88+1898dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | G | GAA | 24 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0003g0220 others(21): Show |
26 | HG00558.hp2 HG00621.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+1897_88+1898dup others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | G | GAAA | 27 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(24): Show |
30 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.88+1896_88+1898dup others(3): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | G | GGA | 6 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0006g0327 others(3): Show |
6 | HG01071.hp1 HG01255.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+1868_88+1869ins others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880687 | |||||||
| chr11:73880687 | G | GGAA | 2 | a0003c0003t0002g0016 a0003c0003t0002g0209 |
3 | HG00642.hp2 HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.88+1868_88+1869ins others(3): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880687 | |||||||
| chr11:73880687 | GA | G | 19 | a0001c0001t0001g0205 a0001c0001t0003g0006 a0001c0001t0003g0007 others(16): Show |
23 | HG00323.hp2 HG00544.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.88+1898delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | GAAAAAAA others(3): Show |
G | 15 | a0001c0001t0001g0208 a0001c0001t0002g0027 a0001c0001t0007g0009 others(12): Show |
16 | HG01106.hp1 HG01975.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.88+1889_88+1898del others(10): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | GAAAAAAA others(4): Show |
G | 46 | a0001c0001t0013g0259 a0001c0001t0013g0260 a0001c0001t0033g0258 others(43): Show |
51 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.88+1888_88+1898del others(11): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0004g0090 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.88+1887_88+1898del others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | GAAAAAAA others(6): Show |
G | 4 | a0001c0001t0004g0093 a0001c0001t0009g0091 a0001c0001t0009g0092 others(1): Show |
4 | NA18953.hp2 NA18961.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+1886_88+1898del others(13): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | GAAAAAAA others(7): Show |
G | 26 | a0001c0001t0004g0012 a0001c0001t0004g0095 a0001c0001t0004g0096 others(23): Show |
27 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.88+1885_88+1898del others(14): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880687 | GAAAAAAA others(8): Show |
G | 1 | a0001c0001t0004g0089 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.88+1884_88+1898del others(15): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73880687 | ||||||
| chr11:73880688 | A | G | 5 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+1869A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880688 | |||||||
| chr11:73880689 | A | G | 2 | a0001c0001t0012g0082 a0001c0001t0015g0083 |
2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.88+1870A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880689 | |||||||
| chr11:73880697 | A | G | 3 | a0001c0001t0007g0034 a0001c0001t0007g0035 a0001c0001t0027g0026 |
3 | HG02717.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.88+1878A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880697 | |||||||
| chr11:73880698 | A | G | 8 | a0001c0001t0002g0027 a0001c0001t0007g0009 a0001c0001t0007g0034 others(5): Show |
9 | HG02615.hp2 HG02717.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+1879A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880698 | |||||||
| chr11:73880699 | A | G | 4 | a0001c0001t0007g0009 a0001c0001t0007g0036 a0001c0001t0007g0037 others(1): Show |
5 | HG02965.hp1 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+1880A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880699 | |||||||
| chr11:73880748 | T | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+1929T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880748 | |||||||
| chr11:73880773 | C | T | 49 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.88+1954C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880773 | |||||||
| chr11:73880859 | G | A | 5 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+2040G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73880859 | |||||||
| chr11:73881150 | A | G | 186 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(183): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.88+2331A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73881150 | |||||||
| chr11:73881270 | T | G | 36 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(33): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.88+2451T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73881270 | |||||||
| chr11:73881414 | T | C | 2 | a0001c0001t0005g0135 a0001c0001t0005g0136 |
2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.88+2595T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73881414 | |||||||
| chr11:73881639 | A | ATGT | 32 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(29): Show |
33 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+2840_88+2842dup others(3): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73881639 | ||||||
| chr11:73881999 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+3180C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73881999 | |||||||
| chr11:73882040 | A | C | 3 | a0001c0001t0006g0319 a0001c0001t0006g0320 a0001c0001t0006g0325 |
3 | HG02559.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.88+3221A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882040 | |||||||
| chr11:73882048 | A | AT | 35 | a0001c0001t0001g0281 a0003c0003t0002g0008 a0003c0003t0002g0021 others(32): Show |
40 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.88+3241dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73882048 | ||||||
| chr11:73882311 | C | CT | 72 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0167 others(69): Show |
78 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.88+3510dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73882311 | ||||||
| chr11:73882311 | CT | C | 39 | a0001c0001t0001g0137 a0001c0001t0001g0168 a0001c0001t0001g0169 others(36): Show |
40 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.88+3510delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73882311 | ||||||
| chr11:73882318 | T | G | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.88+3499T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882318 | |||||||
| chr11:73882345 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+3526A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882345 | |||||||
| chr11:73882358 | T | C | 2 | a0001c0001t0021g0229 a0001c0001t0021g0240 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.88+3539T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882358 | |||||||
| chr11:73882389 | A | C | 9 | a0001c0001t0002g0027 a0001c0001t0007g0009 a0001c0001t0007g0034 others(6): Show |
10 | HG02615.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+3570A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882389 | |||||||
| chr11:73882542 | A | T | 1 | a0002c0002t0002g0046 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.88+3723A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882542 | |||||||
| chr11:73882603 | C | T | 48 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(45): Show |
53 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.88+3784C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882603 | |||||||
| chr11:73882625 | C | T | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+3806C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882625 | |||||||
| chr11:73882634 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+3815G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882634 | |||||||
| chr11:73882768 | A | G | 1 | a0002c0002t0002g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.88+3949A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882768 | |||||||
| chr11:73882794 | G | A | 3 | a0001c0001t0003g0225 a0001c0001t0022g0261 a0001c0001t0022g0262 |
3 | HG02451.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+3975G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882794 | |||||||
| chr11:73882871 | G | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.88+4052G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882871 | |||||||
| chr11:73882882 | C | T | 1 | a0001c0001t0003g0247 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.88+4063C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882882 | |||||||
| chr11:73882954 | C | T | 1 | a0002c0002t0002g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+4135C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882954 | |||||||
| chr11:73882960 | C | G | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+4141C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73882960 | |||||||
| chr11:73883146 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.89-4208C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883146 | |||||||
| chr11:73883156 | C | T | 1 | a0001c0001t0013g0257 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.89-4198C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883156 | |||||||
| chr11:73883204 | C | G | 2 | a0002c0002t0002g0032 a0002c0002t0002g0033 |
2 | NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.89-4150C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883204 | |||||||
| chr11:73883299 | T | G | 1 | a0001c0001t0009g0094 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.89-4055T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883299 | |||||||
| chr11:73883387 | A | G | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-3967A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883387 | |||||||
| chr11:73883520 | T | C | 1 | a0003c0003t0002g0286 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.89-3834T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883520 | |||||||
| chr11:73883675 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-3679C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883675 | |||||||
| chr11:73883678 | G | A | 2 | a0001c0001t0003g0250 a0001c0001t0003g0252 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.89-3676G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883678 | |||||||
| chr11:73883705 | C | T | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-3649C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883705 | |||||||
| chr11:73883706 | G | A | 1 | a0003c0003t0002g0270 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.89-3648G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883706 | |||||||
| chr11:73883709 | C | T | 11 | a0001c0001t0004g0093 a0001c0001t0004g0106 a0001c0001t0009g0088 others(8): Show |
11 | NA18948.hp1 NA18953.hp2 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-3645C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883709 | |||||||
| chr11:73883866 | T | C | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.89-3488T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73883866 | |||||||
| chr11:73884009 | A | G | 1 | a0001c0001t0004g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-3345A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884009 | |||||||
| chr11:73884065 | A | C | 2 | a0001c0001t0004g0114 a0001c0001t0004g0115 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89-3289A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884065 | |||||||
| chr11:73884068 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3286C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884068 | |||||||
| chr11:73884302 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.89-3052C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884302 | |||||||
| chr11:73884307 | C | G | 1 | a0001c0001t0030g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.89-3047C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884307 | |||||||
| chr11:73884401 | G | A | 1 | a0001c0001t0040g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.89-2953G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884401 | |||||||
| chr11:73884442 | C | G | 3 | a0001c0001t0006g0319 a0001c0001t0006g0320 a0001c0001t0006g0325 |
3 | HG02559.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.89-2912C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884442 | |||||||
| chr11:73884731 | C | A | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.89-2623C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884731 | |||||||
| chr11:73884756 | T | G | 1 | a0003c0003t0002g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.89-2598T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884756 | |||||||
| chr11:73884863 | C | CT | 36 | a0001c0001t0001g0163 a0001c0001t0001g0167 a0001c0001t0001g0334 others(33): Show |
36 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-2477dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73884863 | ||||||
| chr11:73884863 | C | G | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.89-2491C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73884863 | |||||||
| chr11:73885016 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-2338C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885016 | |||||||
| chr11:73885284 | C | T | 1 | a0003c0003t0002g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.89-2070C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885284 | |||||||
| chr11:73885303 | C | T | 7 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2051C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885303 | |||||||
| chr11:73885437 | C | T | 1 | a0004c0005t0019g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.89-1917C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885437 | |||||||
| chr11:73885464 | G | A | 49 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.89-1890G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885464 | |||||||
| chr11:73885470 | C | A | 1 | a0002c0002t0028g0048 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.89-1884C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885470 | |||||||
| chr11:73885559 | G | T | 1 | a0001c0001t0003g0238 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.89-1795G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885559 | |||||||
| chr11:73885627 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-1727A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885627 | |||||||
| chr11:73885628 | G | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-1726G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885628 | |||||||
| chr11:73885679 | T | C | 6 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(3): Show |
7 | HG02717.hp1 HG02965.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-1675T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885679 | |||||||
| chr11:73885726 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.89-1628C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885726 | |||||||
| chr11:73885746 | T | G | 86 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(83): Show |
93 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.89-1608T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885746 | |||||||
| chr11:73885810 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1544C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885810 | |||||||
| chr11:73885842 | C | CA | 44 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0264 others(41): Show |
44 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.89-1493dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73885842 | ||||||
| chr11:73885842 | CA | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0205 a0001c0001t0014g0011 others(3): Show |
7 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-1493delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73885842 | ||||||
| chr11:73885979 | A | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-1375A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73885979 | |||||||
| chr11:73886006 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0129 |
2 | NA18950.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.89-1348C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886006 | |||||||
| chr11:73886024 | T | TG | 6 | a0001c0001t0001g0334 a0001c0001t0006g0327 a0001c0001t0006g0329 others(3): Show |
6 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1327dupG | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73886024 | ||||||
| chr11:73886093 | C | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0218 |
3 | HG01070.hp2 HG01071.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.89-1261C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886093 | |||||||
| chr11:73886218 | A | G | 1 | a0002c0002t0002g0075 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.89-1136A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886218 | |||||||
| chr11:73886325 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.89-1029C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886325 | |||||||
| chr11:73886531 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.89-823C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886531 | |||||||
| chr11:73886543 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.89-811G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886543 | |||||||
| chr11:73886577 | G | A | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.89-777G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886577 | |||||||
| chr11:73886672 | C | CA | 43 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0140 others(40): Show |
43 | HG00423.hp1 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-656dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73886672 | ||||||
| chr11:73886672 | C | CAA | 6 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0036 others(3): Show |
7 | HG02055.hp2 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-657_89-656dupAA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73886672 | ||||||
| chr11:73886672 | CA | C | 9 | a0001c0001t0001g0169 a0001c0001t0004g0090 a0001c0001t0004g0114 others(6): Show |
9 | HG00639.hp2 HG02074.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-656delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73886672 | ||||||
| chr11:73886672 | CAA | C | 28 | a0001c0001t0001g0128 a0001c0001t0004g0012 a0001c0001t0004g0093 others(25): Show |
29 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.89-657_89-656delAA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73886672 | ||||||
| chr11:73886672 | CAAAAAAA others(1): Show |
C | 50 | a0001c0001t0001g0212 a0002c0002t0002g0003 a0002c0002t0002g0004 others(47): Show |
55 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.89-663_89-656delAA others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73886672 | ||||||
| chr11:73886672 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0198 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.89-665_89-656delAA others(8): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 73886672 | ||||||
| chr11:73886918 | T | C | 1 | a0001c0001t0027g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-436T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886918 | |||||||
| chr11:73886919 | C | T | 1 | a0003c0003t0002g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.89-435C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73886919 | |||||||
| chr11:73887099 | C | T | 1 | a0002c0002t0002g0074 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.89-255C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73887099 | |||||||
| chr11:73887221 | C | T | 7 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-133C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73887221 | |||||||
| chr11:73887241 | G | A | 34 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(31): Show |
35 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.89-113G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73887241 | |||||||
| chr11:73887329 | G | A | 4 | a0001c0001t0007g0009 a0001c0001t0007g0036 a0001c0001t0007g0037 others(1): Show |
5 | HG02965.hp1 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-25G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 2/11 | chr11 | 73887329 | |||||||
| chr11:73888240 | C | T | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.192+783C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73888240 | |||||||
| chr11:73888361 | C | G | 1 | a0002c0002t0002g0073 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.192+904C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73888361 | |||||||
| chr11:73888449 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.192+992C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73888449 | |||||||
| chr11:73888755 | G | C | 67 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0007g0009 others(64): Show |
73 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.192+1298G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73888755 | |||||||
| chr11:73888971 | G | A | 10 | a0002c0002t0002g0046 a0002c0002t0002g0049 a0002c0002t0002g0051 others(7): Show |
10 | HG03654.hp1 NA18939.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+1514G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73888971 | |||||||
| chr11:73889027 | C | G | 9 | a0001c0001t0002g0027 a0001c0001t0007g0009 a0001c0001t0007g0034 others(6): Show |
10 | HG02615.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+1570C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889027 | |||||||
| chr11:73889122 | G | A | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.192+1665G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889122 | |||||||
| chr11:73889164 | A | G | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+1707A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889164 | |||||||
| chr11:73889179 | T | C | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.192+1722T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889179 | |||||||
| chr11:73889306 | T | C | 49 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(46): Show |
54 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.193-1806T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889306 | |||||||
| chr11:73889802 | A | C | 1 | a0001c0001t0001g0199 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.193-1310A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889802 | |||||||
| chr11:73889843 | G | A | 152 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(149): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.193-1269G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889843 | |||||||
| chr11:73889887 | A | C | 2 | a0001c0001t0004g0114 a0001c0001t0004g0115 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.193-1225A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889887 | |||||||
| chr11:73889909 | C | T | 1 | a0003c0003t0002g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.193-1203C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73889909 | |||||||
| chr11:73890114 | G | A | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.193-998G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890114 | |||||||
| chr11:73890274 | T | G | 1 | a0001c0001t0003g0231 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.193-838T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890274 | |||||||
| chr11:73890356 | A | T | 1 | a0001c0001t0003g0227 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.193-756A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890356 | |||||||
| chr11:73890720 | T | G | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-392T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890720 | |||||||
| chr11:73890743 | G | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.193-369G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890743 | |||||||
| chr11:73890776 | G | A | 4 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-336G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890776 | |||||||
| chr11:73890789 | T | A | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-323T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890789 | |||||||
| chr11:73890878 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0161 a0001c0001t0001g0196 |
3 | HG01515.hp2 HG01517.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.193-234C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73890878 | |||||||
| chr11:73891056 | T | C | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-56T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 3/11 | chr11 | 73891056 | |||||||
| chr11:73891521 | A | G | 3 | a0001c0001t0006g0319 a0001c0001t0006g0320 a0001c0001t0006g0325 |
3 | HG02559.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+320A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891521 | |||||||
| chr11:73891619 | A | T | 1 | a0001c0001t0003g0237 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.282+418A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891619 | |||||||
| chr11:73891636 | G | A | 1 | a0001c0001t0038g0125 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.282+435G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891636 | |||||||
| chr11:73891646 | T | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+445T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891646 | |||||||
| chr11:73891689 | T | G | 5 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+488T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891689 | |||||||
| chr11:73891884 | C | T | 1 | a0001c0001t0004g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.282+683C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891884 | |||||||
| chr11:73891902 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.282+701A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891902 | |||||||
| chr11:73891903 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.282+702A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891903 | |||||||
| chr11:73891905 | G | A | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+704G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73891905 | |||||||
| chr11:73892088 | C | T | 1 | a0001c0001t0027g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+887C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892088 | |||||||
| chr11:73892114 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+913G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892114 | |||||||
| chr11:73892152 | G | C | 1 | a0001c0001t0027g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.282+951G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892152 | |||||||
| chr11:73892174 | A | G | 49 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.282+973A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892174 | |||||||
| chr11:73892288 | A | C | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.282+1087A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892288 | |||||||
| chr11:73892325 | CA | C | 53 | a0001c0001t0001g0195 a0001c0001t0004g0012 a0001c0001t0004g0089 others(50): Show |
55 | HG00558.hp1 HG00735.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.282+1141delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73892325 | ||||||
| chr11:73892392 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0172 |
2 | NA18979.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.282+1191T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892392 | |||||||
| chr11:73892632 | C | T | 1 | a0002c0002t0002g0042 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.282+1431C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892632 | |||||||
| chr11:73892694 | CTG | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+1495_282+1496d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73892694 | ||||||
| chr11:73892729 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+1528G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892729 | |||||||
| chr11:73892752 | T | C | 226 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(223): Show |
245 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.282+1551T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892752 | |||||||
| chr11:73892816 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0173 |
2 | NA18967.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.282+1615G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73892816 | |||||||
| chr11:73893005 | C | G | 2 | a0001c0001t0004g0101 a0001c0001t0004g0102 |
2 | HG01515.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.282+1804C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893005 | |||||||
| chr11:73893112 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.282+1911T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893112 | |||||||
| chr11:73893166 | A | T | 31 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(28): Show |
32 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.282+1965A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893166 | |||||||
| chr11:73893168 | G | T | 1 | a0001c0001t0017g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.282+1967G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893168 | |||||||
| chr11:73893260 | G | A | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.282+2059G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893260 | |||||||
| chr11:73893311 | A | G | 1 | a0002c0002t0002g0056 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.282+2110A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893311 | |||||||
| chr11:73893315 | C | T | 50 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(47): Show |
55 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.282+2114C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893315 | |||||||
| chr11:73893413 | G | A | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+2212G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893413 | |||||||
| chr11:73893694 | G | A | 1 | a0001c0001t0022g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.282+2493G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893694 | |||||||
| chr11:73893738 | C | CA | 18 | a0001c0001t0001g0121 a0001c0001t0001g0141 a0001c0001t0001g0142 others(15): Show |
18 | HG00639.hp2 HG01515.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.282+2560dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73893738 | ||||||
| chr11:73893738 | CA | C | 15 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0003g0231 others(12): Show |
16 | HG01070.hp2 HG01168.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+2560delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73893738 | ||||||
| chr11:73893738 | CAA | C | 148 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(145): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.282+2559_282+2560d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73893738 | ||||||
| chr11:73893738 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0236 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.282+2548_282+2560d others(15): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73893738 | ||||||
| chr11:73893758 | A | G | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.282+2557A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893758 | |||||||
| chr11:73893777 | A | G | 1 | a0003c0003t0002g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.282+2576A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893777 | |||||||
| chr11:73893778 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+2577C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893778 | |||||||
| chr11:73893786 | C | T | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+2585C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893786 | |||||||
| chr11:73893990 | G | C | 1 | a0002c0002t0002g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+2789G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73893990 | |||||||
| chr11:73894018 | G | A | 50 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(47): Show |
55 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.282+2817G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894018 | |||||||
| chr11:73894098 | T | G | 1 | a0001c0001t0008g0313 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.282+2897T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894098 | |||||||
| chr11:73894114 | T | G | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+2913T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894114 | |||||||
| chr11:73894160 | C | G | 1 | a0001c0001t0004g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.282+2959C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894160 | |||||||
| chr11:73894198 | T | G | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.282+2997T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894198 | |||||||
| chr11:73894364 | T | G | 183 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(180): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.282+3163T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894364 | |||||||
| chr11:73894421 | A | G | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.282+3220A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894421 | |||||||
| chr11:73894462 | A | G | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.282+3261A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894462 | |||||||
| chr11:73894537 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.282+3336C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894537 | |||||||
| chr11:73894592 | T | A | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+3391T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894592 | |||||||
| chr11:73894634 | T | TA | 46 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0029 others(43): Show |
50 | HG00544.hp1 HG00733.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.282+3442dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73894634 | ||||||
| chr11:73894781 | G | A | 7 | a0001c0001t0001g0334 a0001c0001t0006g0327 a0001c0001t0006g0329 others(4): Show |
7 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+3580G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894781 | |||||||
| chr11:73894876 | C | G | 1 | a0002c0002t0002g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.282+3675C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894876 | |||||||
| chr11:73894881 | G | A | 5 | a0002c0002t0002g0003 a0002c0002t0002g0043 a0002c0002t0002g0050 others(2): Show |
7 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+3680G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73894881 | |||||||
| chr11:73895188 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.283-3958A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895188 | |||||||
| chr11:73895406 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-3740A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895406 | |||||||
| chr11:73895722 | T | C | 1 | a0001c0001t0003g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.283-3424T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895722 | |||||||
| chr11:73895761 | G | C | 6 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(3): Show |
7 | HG02717.hp1 HG02965.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-3385G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895761 | |||||||
| chr11:73895800 | G | A | 8 | a0002c0002t0002g0003 a0002c0002t0002g0043 a0002c0002t0002g0050 others(5): Show |
10 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-3346G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895800 | |||||||
| chr11:73895876 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0211 a0001c0001t0001g0212 others(5): Show |
9 | HG00733.hp2 HG01081.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-3270G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895876 | |||||||
| chr11:73895914 | C | T | 1 | a0003c0003t0002g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.283-3232C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895914 | |||||||
| chr11:73895918 | G | A | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-3228G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73895918 | |||||||
| chr11:73896141 | T | G | 1 | a0002c0002t0002g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.283-3005T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896141 | |||||||
| chr11:73896205 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.283-2941T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896205 | |||||||
| chr11:73896227 | A | G | 66 | a0001c0001t0002g0027 a0001c0001t0007g0009 a0001c0001t0007g0034 others(63): Show |
72 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.283-2919A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896227 | |||||||
| chr11:73896254 | C | CT | 87 | a0001c0001t0001g0145 a0001c0001t0001g0264 a0001c0001t0001g0267 others(84): Show |
94 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.283-2877dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73896254 | ||||||
| chr11:73896254 | CT | C | 56 | a0001c0001t0001g0148 a0001c0001t0001g0172 a0001c0001t0001g0174 others(53): Show |
61 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.283-2877delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73896254 | ||||||
| chr11:73896295 | CTT | C | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2846_283-2845d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73896295 | ||||||
| chr11:73896306 | AT | A | 216 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(213): Show |
235 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.283-2829delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73896306 | ||||||
| chr11:73896306 | ATT | A | 7 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.283-2830_283-2829d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73896306 | ||||||
| chr11:73896311 | T | A | 4 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2835T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896311 | |||||||
| chr11:73896373 | A | G | 1 | a0002c0002t0002g0049 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.283-2773A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896373 | |||||||
| chr11:73896382 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-2764A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896382 | |||||||
| chr11:73896386 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.283-2760G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896386 | |||||||
| chr11:73896477 | G | A | 1 | a0002c0002t0002g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.283-2669G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896477 | |||||||
| chr11:73896567 | C | T | 49 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.283-2579C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896567 | |||||||
| chr11:73896581 | T | C | 60 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(57): Show |
65 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.283-2565T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896581 | |||||||
| chr11:73896605 | A | G | 49 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.283-2541A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896605 | |||||||
| chr11:73896650 | G | T | 1 | a0003c0006t0002g0297 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.283-2496G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896650 | |||||||
| chr11:73896685 | C | G | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2461C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896685 | |||||||
| chr11:73896714 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0179 |
2 | NA18950.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.283-2432G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896714 | |||||||
| chr11:73896827 | G | T | 1 | a0002c0002t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.283-2319G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896827 | |||||||
| chr11:73896839 | G | A | 4 | a0001c0001t0007g0009 a0001c0001t0007g0036 a0001c0001t0007g0037 others(1): Show |
5 | HG02965.hp1 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-2307G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896839 | |||||||
| chr11:73896886 | G | A | 1 | a0003c0003t0002g0271 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283-2260G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896886 | |||||||
| chr11:73896900 | G | A | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-2246G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896900 | |||||||
| chr11:73896900 | GGACGGGG others(44): Show |
G | 1 | a0001c0001t0001g0159 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.283-2227_283-2177d others(53): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73896900 | ||||||
| chr11:73896922 | G | T | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.283-2224G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896922 | |||||||
| chr11:73896923 | G | C | 1 | a0001c0001t0004g0090 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.283-2223G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896923 | |||||||
| chr11:73896941 | C | T | 5 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-2205C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896941 | |||||||
| chr11:73896944 | C | T | 1 | a0003c0003t0026g0283 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.283-2202C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896944 | |||||||
| chr11:73896951 | C | G | 223 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(220): Show |
242 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.283-2195C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896951 | |||||||
| chr11:73896954 | C | T | 9 | a0001c0001t0002g0027 a0001c0001t0007g0009 a0001c0001t0007g0034 others(6): Show |
10 | HG02615.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-2192C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896954 | |||||||
| chr11:73896970 | G | A | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283-2176G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896970 | |||||||
| chr11:73896972 | G | C | 9 | a0001c0001t0002g0027 a0001c0001t0007g0009 a0001c0001t0007g0034 others(6): Show |
10 | HG02615.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-2174G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73896972 | |||||||
| chr11:73897000 | T | C | 223 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(220): Show |
242 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.283-2146T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897000 | |||||||
| chr11:73897001 | G | A | 7 | a0001c0001t0009g0088 a0001c0001t0009g0091 a0001c0001t0009g0092 others(4): Show |
7 | NA18948.hp1 NA18953.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.283-2145G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897001 | |||||||
| chr11:73897017 | C | G | 1 | a0003c0003t0002g0286 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.283-2129C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897017 | |||||||
| chr11:73897026 | GGGCTCCT others(71): Show |
G | 2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283-2067_283-1990d others(80): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897026 | ||||||
| chr11:73897051 | G | A | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.283-2095G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897051 | |||||||
| chr11:73897071 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283-2075C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897071 | |||||||
| chr11:73897079 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-2067A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897079 | |||||||
| chr11:73897096 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.283-2050G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897096 | |||||||
| chr11:73897104 | T | G | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283-2042T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897104 | |||||||
| chr11:73897119 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-2027C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897119 | |||||||
| chr11:73897125 | G | C | 26 | a0001c0001t0001g0334 a0001c0001t0005g0326 a0001c0001t0006g0310 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-2021G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897125 | |||||||
| chr11:73897166 | G | A | 1 | a0003c0003t0002g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283-1980G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897166 | |||||||
| chr11:73897174 | G | A | 1 | a0003c0003t0002g0288 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.283-1972G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897174 | |||||||
| chr11:73897175 | TGCGGGGG others(42): Show |
T | 2 | a0001c0001t0023g0118 a0001c0001t0038g0125 |
2 | HG02056.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.283-1951_283-1903d others(51): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897175 | ||||||
| chr11:73897183 | G | A | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1963G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897183 | |||||||
| chr11:73897187 | ACCCCCCC others(43): Show |
A | 5 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0305 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1922_283-1873d others(52): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897187 | ||||||
| chr11:73897188 | C | T | 5 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-1958C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897188 | |||||||
| chr11:73897209 | C | G | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.283-1937C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897209 | |||||||
| chr11:73897214 | C | T | 1 | a0001c0001t0004g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.283-1932C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897214 | |||||||
| chr11:73897224 | G | T | 33 | a0001c0001t0003g0247 a0001c0001t0004g0012 a0001c0001t0004g0089 others(30): Show |
34 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.283-1922G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897224 | |||||||
| chr11:73897233 | C | A | 1 | a0001c0001t0003g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.283-1913C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897233 | |||||||
| chr11:73897236 | AC | A | 218 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(215): Show |
237 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.283-1902delC | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897236 | ||||||
| chr11:73897276 | T | C | 36 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(33): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.283-1870T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897276 | |||||||
| chr11:73897277 | G | A | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 |
3 | HG02622.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-1869G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897277 | |||||||
| chr11:73897282 | G | A | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.283-1864G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897282 | |||||||
| chr11:73897321 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-1825A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897321 | |||||||
| chr11:73897323 | G | A | 3 | a0001c0004t0001g0175 a0001c0004t0001g0180 a0001c0004t0001g0193 |
3 | HG02155.hp2 NA18991.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.283-1823G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897323 | |||||||
| chr11:73897343 | CCAGACGG others(33): Show |
C | 2 | a0001c0001t0001g0162 a0001c0001t0030g0028 |
2 | HG02615.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.283-1753_283-1714d others(42): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897343 | ||||||
| chr11:73897348 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.283-1798C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897348 | |||||||
| chr11:73897370 | G | GGCTCCTC others(113): Show |
2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283-1747_283-1746i others(122): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897370 | ||||||
| chr11:73897400 | T | TGGGCGGA others(33): Show |
1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283-1714_283-1713i others(42): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897400 | ||||||
| chr11:73897434 | G | A | 12 | a0001c0001t0005g0326 a0001c0001t0008g0313 a0001c0001t0008g0315 others(9): Show |
12 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.283-1712G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897434 | |||||||
| chr11:73897471 | G | C | 5 | a0001c0001t0001g0141 a0001c0001t0001g0150 a0001c0001t0001g0162 others(2): Show |
5 | HG00621.hp1 HG00673.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-1675G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897471 | |||||||
| chr11:73897472 | G | T | 2 | a0001c0001t0002g0027 a0001c0001t0030g0028 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.283-1674G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897472 | |||||||
| chr11:73897553 | C | T | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283-1593C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897553 | |||||||
| chr11:73897554 | G | T | 6 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(3): Show |
7 | HG02717.hp1 HG02965.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1592G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897554 | |||||||
| chr11:73897626 | TGGCGGCC others(30): Show |
T | 5 | a0001c0001t0001g0143 a0001c0001t0013g0257 a0001c0001t0013g0259 others(2): Show |
5 | HG01106.hp1 HG02738.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-1479_283-1443d others(39): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897626 | ||||||
| chr11:73897630 | G | A | 1 | a0002c0002t0002g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.283-1516G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897630 | |||||||
| chr11:73897729 | C | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-1417C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897729 | |||||||
| chr11:73897743 | G | A | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1403G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897743 | |||||||
| chr11:73897884 | TG | T | 223 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(220): Show |
242 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.283-1258delG | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73897884 | ||||||
| chr11:73897910 | C | T | 11 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0031 others(8): Show |
11 | HG00544.hp1 NA18968.hp2 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.283-1236C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897910 | |||||||
| chr11:73897911 | G | A | 49 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.283-1235G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897911 | |||||||
| chr11:73897938 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-1208C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897938 | |||||||
| chr11:73897966 | T | C | 183 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(180): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.283-1180T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897966 | |||||||
| chr11:73897973 | G | A | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-1173G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73897973 | |||||||
| chr11:73898037 | G | T | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-1109G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898037 | |||||||
| chr11:73898044 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.283-1102G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898044 | |||||||
| chr11:73898048 | C | T | 31 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(28): Show |
32 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.283-1098C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898048 | |||||||
| chr11:73898158 | G | A | 49 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(46): Show |
54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.283-988G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898158 | |||||||
| chr11:73898164 | G | A | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.283-982G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898164 | |||||||
| chr11:73898191 | G | GGGGAGAG others(15): Show |
4 | a0001c0001t0007g0009 a0001c0001t0007g0036 a0001c0001t0007g0037 others(1): Show |
5 | HG02965.hp1 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-951_283-930dup others(22): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73898191 | ||||||
| chr11:73898217 | GGAGGGA | G | 54 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0152 others(51): Show |
59 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.283-902_283-897del others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73898217 | ||||||
| chr11:73898229 | A | G | 1 | a0002c0002t0002g0041 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.283-917A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898229 | |||||||
| chr11:73898238 | GGGAGAGG others(5): Show |
G | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 |
3 | HG02622.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-896_283-885del others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73898238 | ||||||
| chr11:73898244 | GGGAGAA | G | 29 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(26): Show |
30 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.283-896_283-891del others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73898244 | ||||||
| chr11:73898454 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.283-692A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898454 | |||||||
| chr11:73898551 | G | A | 1 | a0001c0001t0022g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.283-595G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898551 | |||||||
| chr11:73898617 | G | C | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 |
3 | HG02622.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.283-529G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898617 | |||||||
| chr11:73898661 | T | G | 10 | a0002c0002t0002g0046 a0002c0002t0002g0049 a0002c0002t0002g0051 others(7): Show |
10 | HG03654.hp1 NA18939.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.283-485T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898661 | |||||||
| chr11:73898687 | G | A | 34 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(31): Show |
35 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.283-459G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898687 | |||||||
| chr11:73898811 | TCAAA | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-314_283-311del others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73898811 | ||||||
| chr11:73898832 | CAAAT | C | 6 | a0001c0001t0003g0250 a0001c0001t0003g0251 a0001c0001t0003g0252 others(3): Show |
6 | HG01074.hp1 HG01099.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-305_283-302del others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73898832 | ||||||
| chr11:73898928 | T | C | 1 | a0002c0002t0002g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.283-218T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73898928 | |||||||
| chr11:73899033 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0023g0118 a0001c0001t0038g0125 |
3 | HG02056.hp1 NA18612.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.283-113C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73899033 | |||||||
| chr11:73899065 | A | C | 186 | a0001c0001t0001g0264 a0001c0001t0001g0267 a0001c0001t0001g0268 others(183): Show |
199 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.283-81A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | chr11 | 73899065 | |||||||
| chr11:73899105 | TTCATTAT others(13): Show |
T | 1 | a0003c0003t0031g0284 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.283-39_283-20delCA others(18): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 73899105 | ||||||
| chr11:73899408 | C | CT | 51 | a0001c0001t0001g0162 a0001c0001t0001g0191 a0001c0001t0001g0192 others(48): Show |
58 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.381+187dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 73899408 | ||||||
| chr11:73899408 | C | CTT | 6 | a0001c0001t0003g0228 a0001c0001t0003g0231 a0001c0001t0013g0257 others(3): Show |
6 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+186_381+187dup others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 73899408 | ||||||
| chr11:73899408 | CT | C | 27 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0001g0137 others(24): Show |
27 | HG00639.hp2 HG01168.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.381+187delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 73899408 | ||||||
| chr11:73899408 | CTTTTT | C | 47 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(44): Show |
52 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.381+183_381+187del others(5): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 73899408 | ||||||
| chr11:73899514 | C | T | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+270C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73899514 | |||||||
| chr11:73899608 | C | T | 1 | a0002c0002t0002g0307 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.381+364C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73899608 | |||||||
| chr11:73899666 | C | A | 2 | a0001c0001t0002g0337 a0001c0001t0003g0238 |
2 | HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.381+422C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73899666 | |||||||
| chr11:73899701 | C | T | 1 | a0001c0001t0027g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.381+457C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73899701 | |||||||
| chr11:73899812 | G | A | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.382-458G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73899812 | |||||||
| chr11:73899868 | T | A | 1 | a0003c0003t0031g0284 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.382-402T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73899868 | |||||||
| chr11:73899971 | T | C | 229 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0003g0006 others(226): Show |
248 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.382-299T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73899971 | |||||||
| chr11:73900001 | CTT | C | 145 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0004g0012 others(142): Show |
158 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.382-255_382-254del others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 73900001 | ||||||
| chr11:73900069 | G | C | 1 | a0003c0003t0031g0284 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.382-201G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 5/11 | chr11 | 73900069 | |||||||
| chr11:73900433 | C | G | 130 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(127): Show |
138 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.532+13C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900433 | |||||||
| chr11:73900464 | A | G | 1 | a0002c0002t0002g0056 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.532+44A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900464 | |||||||
| chr11:73900475 | A | G | 64 | a0001c0001t0002g0337 a0001c0001t0007g0009 a0001c0001t0007g0034 others(61): Show |
70 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.532+55A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900475 | |||||||
| chr11:73900764 | C | G | 18 | a0003c0003t0002g0008 a0003c0003t0002g0021 a0003c0003t0002g0023 others(15): Show |
22 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.532+344C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900764 | |||||||
| chr11:73900765 | G | A | 1 | a0001c0001t0003g0242 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.532+345G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900765 | |||||||
| chr11:73900778 | G | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+358G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900778 | |||||||
| chr11:73900801 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.532+381T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900801 | |||||||
| chr11:73900834 | T | G | 1 | a0001c0001t0005g0202 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.532+414T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900834 | |||||||
| chr11:73900839 | G | A | 40 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0018 others(37): Show |
46 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.532+419G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900839 | |||||||
| chr11:73900871 | A | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+451A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900871 | |||||||
| chr11:73900944 | T | A | 1 | a0003c0003t0031g0284 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.532+524T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73900944 | |||||||
| chr11:73900981 | C | CA | 42 | a0001c0001t0001g0153 a0001c0001t0001g0191 a0001c0001t0001g0205 others(39): Show |
44 | HG00558.hp2 HG00621.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.532+594dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73900981 | ||||||
| chr11:73900981 | CA | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(71): Show |
82 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.532+594delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73900981 | ||||||
| chr11:73900981 | CAA | C | 20 | a0001c0001t0001g0133 a0001c0001t0004g0012 a0001c0001t0004g0089 others(17): Show |
22 | HG01074.hp2 HG01081.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.532+593_532+594del others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73900981 | ||||||
| chr11:73900981 | CAAA | C | 15 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0114 others(12): Show |
16 | HG01106.hp1 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.532+592_532+594del others(3): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73900981 | ||||||
| chr11:73900981 | CAAAA | C | 6 | a0001c0001t0004g0111 a0001c0001t0004g0112 a0001c0001t0004g0113 others(3): Show |
6 | HG02451.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+591_532+594del others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73900981 | ||||||
| chr11:73900981 | CAAAAAAA others(7): Show |
C | 27 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(24): Show |
27 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.532+581_532+594del others(14): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73900981 | ||||||
| chr11:73900981 | CAAAAAAA others(8): Show |
C | 52 | a0001c0001t0022g0261 a0001c0001t0022g0262 a0002c0002t0002g0003 others(49): Show |
57 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.532+580_532+594del others(15): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73900981 | ||||||
| chr11:73901065 | G | A | 1 | a0003c0003t0002g0273 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.532+645G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901065 | |||||||
| chr11:73901073 | G | A | 5 | a0001c0001t0005g0132 a0001c0001t0005g0202 a0001c0001t0005g0203 others(2): Show |
5 | HG02145.hp2 HG03041.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.532+653G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901073 | |||||||
| chr11:73901086 | TAGAG | T | 24 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(21): Show |
24 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.532+675_532+678del others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73901086 | ||||||
| chr11:73901198 | T | TA | 36 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(33): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.532+778_532+779ins others(1): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901198 | |||||||
| chr11:73901476 | A | G | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+1056A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901476 | |||||||
| chr11:73901538 | A | T | 4 | a0001c0001t0003g0250 a0001c0001t0003g0251 a0001c0001t0003g0252 others(1): Show |
4 | HG01099.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+1118A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901538 | |||||||
| chr11:73901566 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+1146C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901566 | |||||||
| chr11:73901571 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+1151C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901571 | |||||||
| chr11:73901605 | AT | A | 9 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0003g0243 others(6): Show |
10 | HG01169.hp2 HG01515.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.532+1200delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73901605 | ||||||
| chr11:73901667 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.532+1247A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901667 | |||||||
| chr11:73901711 | C | T | 2 | a0001c0001t0004g0101 a0001c0001t0004g0102 |
2 | HG01515.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.532+1291C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901711 | |||||||
| chr11:73901714 | G | A | 1 | a0003c0003t0002g0292 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.532+1294G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901714 | |||||||
| chr11:73901822 | C | T | 1 | a0001c0004t0001g0180 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.532+1402C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73901822 | |||||||
| chr11:73901870 | C | CT | 31 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(28): Show |
31 | HG00597.hp1 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.532+1469dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73901870 | ||||||
| chr11:73901870 | CT | C | 7 | a0001c0001t0001g0184 a0001c0001t0001g0201 a0001c0001t0004g0116 others(4): Show |
7 | HG01070.hp2 HG01256.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.532+1469delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73901870 | ||||||
| chr11:73901870 | CTT | C | 33 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(30): Show |
35 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.532+1468_532+1469d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73901870 | ||||||
| chr11:73902061 | C | T | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.532+1641C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902061 | |||||||
| chr11:73902144 | G | A | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+1724G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902144 | |||||||
| chr11:73902192 | C | A | 1 | a0002c0002t0002g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.532+1772C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902192 | |||||||
| chr11:73902195 | T | G | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.532+1775T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902195 | |||||||
| chr11:73902239 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.532+1819C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902239 | |||||||
| chr11:73902280 | G | A | 1 | a0001c0001t0036g0171 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.532+1860G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902280 | |||||||
| chr11:73902417 | T | A | 1 | a0002c0002t0002g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.532+1997T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902417 | |||||||
| chr11:73902655 | G | GT | 109 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(106): Show |
117 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.532+2235_532+2236i others(3): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902655 | |||||||
| chr11:73902715 | G | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+2295G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902715 | |||||||
| chr11:73902757 | C | T | 1 | a0002c0002t0002g0064 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.532+2337C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902757 | |||||||
| chr11:73902812 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0156 a0001c0001t0001g0192 others(1): Show |
5 | NA18961.hp2 NA19055.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.532+2392G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902812 | |||||||
| chr11:73902812 | G | T | 220 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0003g0006 others(217): Show |
240 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.532+2392G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902812 | |||||||
| chr11:73902894 | T | A | 1 | a0001c0001t0001g0191 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.532+2474T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73902894 | |||||||
| chr11:73903239 | A | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+2819A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73903239 | |||||||
| chr11:73903364 | C | T | 105 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(102): Show |
113 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.532+2944C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73903364 | |||||||
| chr11:73903387 | A | G | 1 | a0001c0001t0003g0231 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.532+2967A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73903387 | |||||||
| chr11:73903445 | T | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+3025T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73903445 | |||||||
| chr11:73903487 | C | T | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+3067C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73903487 | |||||||
| chr11:73903499 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.532+3079C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73903499 | |||||||
| chr11:73903716 | CA | C | 94 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0095 others(91): Show |
101 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.532+3310delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73903716 | ||||||
| chr11:73903830 | T | A | 3 | a0001c0001t0006g0319 a0001c0001t0006g0320 a0001c0001t0006g0325 |
3 | HG02559.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.532+3410T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73903830 | |||||||
| chr11:73904091 | A | G | 1 | a0003c0003t0002g0291 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.532+3671A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904091 | |||||||
| chr11:73904097 | G | A | 1 | a0003c0003t0002g0273 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.532+3677G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904097 | |||||||
| chr11:73904301 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0145 a0001c0001t0001g0184 |
3 | HG00423.hp1 HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.532+3881C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904301 | |||||||
| chr11:73904457 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.532+4037G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904457 | |||||||
| chr11:73904554 | G | A | 44 | a0003c0003t0002g0008 a0003c0003t0002g0016 a0003c0003t0002g0021 others(41): Show |
50 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.532+4134G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904554 | |||||||
| chr11:73904669 | T | G | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.532+4249T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904669 | |||||||
| chr11:73904682 | G | A | 220 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0003g0006 others(217): Show |
240 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.532+4262G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904682 | |||||||
| chr11:73904717 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+4297C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904717 | |||||||
| chr11:73904742 | A | ATAATT | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.532+4325_532+4326i others(7): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73904742 | ||||||
| chr11:73904818 | T | C | 2 | a0001c0001t0006g0327 a0001c0001t0006g0332 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.532+4398T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904818 | |||||||
| chr11:73904851 | T | C | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.532+4431T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73904851 | |||||||
| chr11:73905076 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.533-4323C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905076 | |||||||
| chr11:73905225 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.533-4174G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905225 | |||||||
| chr11:73905230 | C | T | 2 | a0004c0005t0019g0069 a0004c0005t0019g0076 |
2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.533-4169C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905230 | |||||||
| chr11:73905237 | T | C | 6 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0001c0001t0003g0222 others(3): Show |
6 | HG02055.hp1 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-4162T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905237 | |||||||
| chr11:73905350 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.533-4049A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905350 | |||||||
| chr11:73905600 | T | G | 1 | a0003c0003t0032g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.533-3799T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905600 | |||||||
| chr11:73905607 | G | T | 12 | a0001c0001t0003g0007 a0001c0001t0003g0018 a0001c0001t0003g0226 others(9): Show |
15 | HG02165.hp2 HG02273.hp1 NA18941.hp1 others(12): Show |
intron_variant | MODIFIER | c.533-3792G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905607 | |||||||
| chr11:73905672 | A | G | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.533-3727A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73905672 | |||||||
| chr11:73906113 | A | G | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.533-3286A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906113 | |||||||
| chr11:73906159 | T | TAG | 39 | a0002c0002t0002g0004 a0002c0002t0002g0010 a0002c0002t0002g0024 others(36): Show |
42 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.533-3240_533-3239i others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906159 | |||||||
| chr11:73906246 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.533-3153C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906246 | |||||||
| chr11:73906253 | TTTTG | T | 26 | a0001c0001t0001g0264 a0001c0001t0004g0012 a0001c0001t0004g0089 others(23): Show |
27 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.533-3130_533-3127d others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73906253 | ||||||
| chr11:73906322 | C | T | 2 | a0001c0001t0001g0122 a0003c0003t0031g0284 |
2 | NA19001.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.533-3077C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906322 | |||||||
| chr11:73906440 | C | T | 1 | a0002c0002t0002g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.533-2959C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906440 | |||||||
| chr11:73906452 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.533-2947C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906452 | |||||||
| chr11:73906510 | C | T | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.533-2889C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906510 | |||||||
| chr11:73906599 | T | C | 1 | a0001c0001t0034g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.533-2800T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906599 | |||||||
| chr11:73906633 | A | C | 1 | a0001c0001t0042g0249 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.533-2766A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906633 | |||||||
| chr11:73906985 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.533-2414A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906985 | |||||||
| chr11:73906986 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.533-2413C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73906986 | |||||||
| chr11:73907142 | T | C | 24 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(21): Show |
24 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.533-2257T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907142 | |||||||
| chr11:73907149 | G | C | 1 | a0001c0001t0022g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.533-2250G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907149 | |||||||
| chr11:73907177 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.533-2222A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907177 | |||||||
| chr11:73907399 | G | A | 24 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(21): Show |
24 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.533-2000G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907399 | |||||||
| chr11:73907412 | C | G | 1 | a0003c0003t0002g0280 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.533-1987C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907412 | |||||||
| chr11:73907425 | G | A | 3 | a0003c0003t0002g0016 a0003c0003t0002g0209 a0003c0003t0002g0210 |
4 | HG00642.hp2 HG01255.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-1974G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907425 | |||||||
| chr11:73907479 | C | T | 53 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(50): Show |
58 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.533-1920C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907479 | |||||||
| chr11:73907648 | C | A | 1 | a0001c0001t0004g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.533-1751C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907648 | |||||||
| chr11:73907666 | G | T | 11 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(8): Show |
12 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.533-1733G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907666 | |||||||
| chr11:73907692 | A | G | 1 | a0004c0005t0019g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.533-1707A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907692 | |||||||
| chr11:73907843 | TA | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.533-1555delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73907843 | |||||||
| chr11:73908127 | C | T | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.533-1272C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908127 | |||||||
| chr11:73908255 | ATGTATAT others(3): Show |
A | 7 | a0001c0001t0007g0037 a0001c0001t0007g0038 a0001c0001t0013g0257 others(4): Show |
7 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-1122_533-1113d others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908255 | ||||||
| chr11:73908259 | A | G | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.533-1140A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908259 | |||||||
| chr11:73908285 | GTA | G | 33 | a0001c0001t0001g0174 a0001c0001t0004g0012 a0001c0001t0004g0089 others(30): Show |
34 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.533-1106_533-1105d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908285 | ||||||
| chr11:73908287 | A | G | 1 | a0001c0001t0007g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.533-1112A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908287 | |||||||
| chr11:73908295 | G | GTGTGTAT others(13): Show |
7 | a0002c0002t0002g0003 a0002c0002t0002g0043 a0002c0002t0002g0050 others(4): Show |
9 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.533-1070_533-1051d others(22): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908295 | ||||||
| chr11:73908295 | G | GTGTGTGT others(13): Show |
2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.533-1099_533-1098i others(22): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908295 | ||||||
| chr11:73908295 | GTGTGTAT others(13): Show |
G | 2 | a0001c0001t0002g0027 a0001c0001t0030g0028 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.533-1070_533-1051d others(22): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908295 | ||||||
| chr11:73908297 | G | A | 1 | a0001c0001t0007g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.533-1102G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908297 | |||||||
| chr11:73908299 | G | A | 1 | a0001c0001t0007g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.533-1100G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908299 | |||||||
| chr11:73908305 | A | G | 1 | a0001c0001t0007g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.533-1094A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908305 | |||||||
| chr11:73908307 | G | GTA | 3 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0001t0001g0170 |
3 | HG00738.hp1 HG02300.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.533-1084_533-1083d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908307 | ||||||
| chr11:73908309 | A | G | 1 | a0001c0001t0007g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.533-1090A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908309 | |||||||
| chr11:73908319 | G | A | 1 | a0001c0001t0007g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.533-1080G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908319 | |||||||
| chr11:73908329 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0281 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.533-1048_533-1039d others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908329 | ||||||
| chr11:73908329 | A | G | 2 | a0001c0001t0007g0034 a0003c0003t0002g0270 |
2 | HG02717.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.533-1070A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908329 | |||||||
| chr11:73908329 | ATATATAT others(3): Show |
A | 40 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0018 others(37): Show |
46 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.533-1048_533-1039d others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908329 | ||||||
| chr11:73908337 | GTGTATAT others(11): Show |
G | 1 | a0003c0003t0002g0270 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.533-1058_533-1041d others(20): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908337 | ||||||
| chr11:73908339 | G | A | 1 | a0001c0001t0007g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.533-1060G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908339 | |||||||
| chr11:73908341 | A | G | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.533-1058A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908341 | |||||||
| chr11:73908361 | G | A | 2 | a0001c0001t0017g0087 a0003c0003t0002g0270 |
2 | NA18972.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.533-1038G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908361 | |||||||
| chr11:73908361 | G | GTA | 36 | a0003c0003t0002g0008 a0003c0003t0002g0016 a0003c0003t0002g0021 others(33): Show |
42 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.533-1028_533-1027d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908361 | ||||||
| chr11:73908389 | A | ATATATAT others(5): Show |
3 | a0001c0001t0002g0337 a0001c0001t0015g0081 a0001c0001t0015g0083 |
3 | HG01358.hp1 HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.533-1001_533-1000i others(14): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908389 | ||||||
| chr11:73908389 | A | ATATATAT others(3): Show |
102 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(99): Show |
110 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.533-1008_533-999du others(11): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908389 | ||||||
| chr11:73908401 | G | A | 132 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(129): Show |
140 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.533-998G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908401 | |||||||
| chr11:73908409 | A | G | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-990A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908409 | |||||||
| chr11:73908415 | G | GTA | 3 | a0001c0001t0013g0259 a0003c0003t0002g0266 a0003c0003t0002g0285 |
3 | HG02300.hp1 HG02886.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.533-972_533-971dup others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 73908415 | ||||||
| chr11:73908490 | G | A | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.533-909G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908490 | |||||||
| chr11:73908567 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.533-832A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908567 | |||||||
| chr11:73908804 | T | C | 1 | a0001c0001t0040g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533-595T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908804 | |||||||
| chr11:73908809 | T | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.533-590T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908809 | |||||||
| chr11:73908849 | C | T | 4 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-550C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908849 | |||||||
| chr11:73908888 | G | A | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-511G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908888 | |||||||
| chr11:73908961 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.533-438A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73908961 | |||||||
| chr11:73909072 | C | A | 2 | a0001c0001t0040g0299 a0001c0008t0039g0263 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.533-327C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73909072 | |||||||
| chr11:73909104 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.533-295A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73909104 | |||||||
| chr11:73909331 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.533-68C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 6/11 | chr11 | 73909331 | |||||||
| chr11:73909795 | G | A | 1 | a0001c0001t0004g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.727+202G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73909795 | |||||||
| chr11:73909855 | C | T | 1 | a0003c0003t0002g0287 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.727+262C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73909855 | |||||||
| chr11:73910360 | T | G | 220 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0003g0006 others(217): Show |
240 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.727+767T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73910360 | |||||||
| chr11:73910756 | C | T | 4 | a0001c0001t0005g0303 a0001c0001t0005g0304 a0001c0001t0005g0305 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1163C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73910756 | |||||||
| chr11:73910848 | G | A | 1 | a0003c0003t0002g0273 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.727+1255G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73910848 | |||||||
| chr11:73910886 | A | G | 1 | a0003c0003t0002g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.727+1293A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73910886 | |||||||
| chr11:73910989 | C | CA | 17 | a0001c0001t0001g0120 a0001c0001t0001g0130 a0001c0001t0001g0138 others(14): Show |
17 | HG00621.hp1 HG00621.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.727+1418dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 73910989 | ||||||
| chr11:73910989 | CA | C | 118 | a0001c0001t0001g0181 a0001c0001t0002g0337 a0001c0001t0004g0012 others(115): Show |
125 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.727+1418delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 73910989 | ||||||
| chr11:73910989 | CAA | C | 5 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0002c0002t0002g0068 others(2): Show |
6 | HG01884.hp2 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.727+1417_727+1418d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 73910989 | ||||||
| chr11:73911019 | G | A | 2 | a0001c0001t0007g0034 a0001c0001t0007g0035 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.727+1426G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911019 | |||||||
| chr11:73911138 | C | T | 1 | a0001c0001t0009g0088 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.727+1545C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911138 | |||||||
| chr11:73911333 | C | T | 1 | a0003c0003t0002g0286 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.727+1740C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911333 | |||||||
| chr11:73911448 | G | A | 30 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0018 others(27): Show |
36 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.727+1855G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911448 | |||||||
| chr11:73911559 | T | C | 3 | a0001c0001t0006g0319 a0001c0001t0006g0320 a0001c0001t0006g0325 |
3 | HG02559.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.727+1966T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911559 | |||||||
| chr11:73911622 | C | CT | 50 | a0001c0001t0001g0176 a0001c0001t0002g0027 a0001c0001t0004g0110 others(47): Show |
56 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.727+2048dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 73911622 | ||||||
| chr11:73911710 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+2117C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911710 | |||||||
| chr11:73911758 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.727+2165C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911758 | |||||||
| chr11:73911785 | C | G | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+2192C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911785 | |||||||
| chr11:73911789 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.727+2196A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911789 | |||||||
| chr11:73911877 | A | G | 36 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(33): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.727+2284A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911877 | |||||||
| chr11:73911882 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+2289C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911882 | |||||||
| chr11:73911957 | A | G | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.727+2364A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73911957 | |||||||
| chr11:73912050 | C | T | 1 | a0001c0001t0008g0316 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.728-2363C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912050 | |||||||
| chr11:73912298 | A | G | 24 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(21): Show |
25 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.728-2115A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912298 | |||||||
| chr11:73912542 | G | A | 1 | a0001c0001t0017g0107 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.728-1871G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912542 | |||||||
| chr11:73912651 | T | C | 1 | a0002c0002t0002g0044 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.728-1762T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912651 | |||||||
| chr11:73912701 | A | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.728-1712A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912701 | |||||||
| chr11:73912845 | A | G | 1 | a0001c0001t0030g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728-1568A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912845 | |||||||
| chr11:73912849 | C | G | 1 | a0001c0001t0011g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.728-1564C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912849 | |||||||
| chr11:73912912 | T | A | 1 | a0001c0001t0040g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728-1501T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73912912 | |||||||
| chr11:73913166 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.728-1247C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913166 | |||||||
| chr11:73913224 | C | A | 1 | a0001c0001t0041g0219 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.728-1189C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913224 | |||||||
| chr11:73913256 | G | A | 11 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(8): Show |
12 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.728-1157G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913256 | |||||||
| chr11:73913369 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.728-1044C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913369 | |||||||
| chr11:73913441 | T | C | 1 | a0001c0008t0039g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728-972T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913441 | |||||||
| chr11:73913449 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.728-964A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913449 | |||||||
| chr11:73913661 | G | A | 4 | a0002c0002t0002g0003 a0002c0002t0002g0043 a0002c0002t0002g0050 others(1): Show |
6 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.728-752G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913661 | |||||||
| chr11:73913692 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.728-705_728-694del others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 73913692 | ||||||
| chr11:73913700 | G | GA | 101 | a0001c0001t0001g0336 a0001c0001t0006g0310 a0001c0001t0006g0318 others(98): Show |
108 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.728-702dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 73913700 | ||||||
| chr11:73913700 | G | GAA | 32 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.728-703_728-702dup others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 73913700 | ||||||
| chr11:73913761 | G | A | 24 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(21): Show |
24 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.728-652G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913761 | |||||||
| chr11:73913765 | G | A | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.728-648G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913765 | |||||||
| chr11:73913843 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.728-570A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913843 | |||||||
| chr11:73913868 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.728-545G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73913868 | |||||||
| chr11:73914081 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.728-332C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73914081 | |||||||
| chr11:73914117 | G | T | 17 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(14): Show |
17 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.728-296G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 7/11 | chr11 | 73914117 | |||||||
| chr11:73914524 | C | A | 7 | a0001c0001t0006g0327 a0001c0001t0006g0329 a0001c0001t0006g0330 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.819+20C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73914524 | |||||||
| chr11:73914697 | C | CT | 30 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0216 others(27): Show |
30 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.819+211dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 73914697 | ||||||
| chr11:73914737 | C | A | 2 | a0001c0001t0020g0185 a0001c0001t0020g0206 |
2 | HG01496.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.819+233C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73914737 | |||||||
| chr11:73914763 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.819+259C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73914763 | |||||||
| chr11:73914788 | A | G | 40 | a0002c0002t0002g0004 a0002c0002t0002g0010 a0002c0002t0002g0024 others(37): Show |
43 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.819+284A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73914788 | |||||||
| chr11:73914948 | G | A | 1 | a0001c0001t0040g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.819+444G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73914948 | |||||||
| chr11:73914970 | A | G | 36 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(33): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.819+466A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73914970 | |||||||
| chr11:73915046 | A | G | 1 | a0001c0001t0004g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.819+542A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915046 | |||||||
| chr11:73915165 | G | C | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+661G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915165 | |||||||
| chr11:73915250 | T | C | 1 | a0004c0005t0019g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.819+746T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915250 | |||||||
| chr11:73915302 | T | A | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+798T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915302 | |||||||
| chr11:73915334 | A | G | 38 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(35): Show |
40 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.819+830A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915334 | |||||||
| chr11:73915530 | C | T | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1015C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915530 | |||||||
| chr11:73915565 | G | A | 11 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(8): Show |
12 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.820-980G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915565 | |||||||
| chr11:73915653 | C | T | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.820-892C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915653 | |||||||
| chr11:73915755 | T | C | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-790T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915755 | |||||||
| chr11:73915771 | T | G | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.820-774T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915771 | |||||||
| chr11:73915775 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.820-770C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915775 | |||||||
| chr11:73915776 | G | A | 2 | a0001c0001t0003g0228 a0001c0001t0003g0239 |
2 | HG00323.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.820-769G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915776 | |||||||
| chr11:73915910 | C | T | 53 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(50): Show |
58 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.820-635C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915910 | |||||||
| chr11:73915947 | C | G | 4 | a0001c0001t0007g0009 a0001c0001t0007g0036 a0001c0001t0007g0037 others(1): Show |
5 | HG02965.hp1 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-598C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73915947 | |||||||
| chr11:73916029 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.820-516T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73916029 | |||||||
| chr11:73916311 | C | CAGAGTAT others(5): Show |
53 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0010 others(50): Show |
58 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.820-232_820-221dup others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 73916311 | ||||||
| chr11:73916348 | A | G | 1 | a0003c0003t0002g0298 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.820-197A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73916348 | |||||||
| chr11:73916464 | A | G | 1 | a0001c0001t0007g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.820-81A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73916464 | |||||||
| chr11:73916533 | A | G | 1 | a0001c0001t0003g0246 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.820-12A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 8/11 | chr11 | 73916533 | |||||||
| chr11:73916701 | A | T | 1 | a0001c0001t0034g0197 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.935+41A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73916701 | |||||||
| chr11:73916739 | A | G | 1 | a0003c0003t0018g0277 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.935+79A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73916739 | |||||||
| chr11:73916750 | A | G | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.935+90A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73916750 | |||||||
| chr11:73916794 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.935+134C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73916794 | |||||||
| chr11:73916819 | A | C | 7 | a0003c0003t0002g0266 a0003c0003t0002g0269 a0003c0003t0002g0285 others(4): Show |
7 | HG00639.hp1 HG01168.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.935+159A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73916819 | |||||||
| chr11:73917011 | A | G | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+351A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73917011 | |||||||
| chr11:73917277 | C | T | 1 | a0001c0001t0006g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.935+617C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73917277 | |||||||
| chr11:73917377 | T | C | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.935+717T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73917377 | |||||||
| chr11:73917535 | G | A | 2 | a0001c0001t0040g0299 a0001c0008t0039g0263 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.935+875G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73917535 | |||||||
| chr11:73917598 | G | A | 2 | a0002c0002t0002g0046 a0002c0002t0002g0073 |
2 | NA18944.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.935+938G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73917598 | |||||||
| chr11:73917870 | C | CAA | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.936-1064_936-1063d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73917870 | ||||||
| chr11:73917870 | CA | C | 7 | a0001c0001t0001g0147 a0001c0001t0001g0153 a0001c0001t0001g0190 others(4): Show |
7 | HG02300.hp1 HG03654.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.936-1063delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73917870 | ||||||
| chr11:73917922 | A | C | 1 | a0003c0003t0002g0291 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.936-1028A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73917922 | |||||||
| chr11:73918274 | T | G | 1 | a0002c0002t0002g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.936-676T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918274 | |||||||
| chr11:73918342 | C | G | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.936-608C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918342 | |||||||
| chr11:73918352 | A | AT | 32 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0120 others(29): Show |
34 | HG01071.hp2 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.936-567dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | AT | A | 32 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0176 others(29): Show |
35 | HG01168.hp2 HG01169.hp1 HG02074.hp1 others(32): Show |
intron_variant | MODIFIER | c.936-567delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | ATT | A | 84 | a0001c0001t0001g0129 a0001c0001t0001g0149 a0001c0001t0001g0169 others(81): Show |
96 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.936-568_936-567del others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | ATTT | A | 54 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0001c0001t0003g0222 others(51): Show |
57 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.936-569_936-567del others(3): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | ATTTT | A | 7 | a0001c0001t0002g0027 a0001c0001t0003g0227 a0001c0001t0003g0238 others(4): Show |
7 | HG00639.hp1 HG02602.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.936-570_936-567del others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | ATTTTTTT others(2): Show |
A | 11 | a0001c0001t0008g0313 a0001c0001t0008g0315 a0001c0001t0008g0316 others(8): Show |
11 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.936-575_936-567del others(9): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0008g0317 a0003c0003t0002g0287 |
2 | HG02698.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.936-576_936-567del others(10): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.936-577_936-567del others(11): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918352 | ATTTTTTT others(9): Show |
A | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-582_936-567del others(16): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918352 | ||||||
| chr11:73918361 | T | TTG | 6 | a0001c0001t0004g0090 a0001c0001t0004g0106 a0001c0001t0004g0109 others(3): Show |
6 | HG02074.hp2 HG02572.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-588_936-587ins others(2): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918361 | ||||||
| chr11:73918362 | T | TG | 24 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0093 others(21): Show |
25 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.936-588_936-587ins others(1): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918362 | |||||||
| chr11:73918363 | T | C | 23 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0018 others(20): Show |
29 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.936-587T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918363 | |||||||
| chr11:73918364 | T | C | 15 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0001c0001t0003g0222 others(12): Show |
15 | HG01099.hp2 HG01257.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.936-586T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918364 | |||||||
| chr11:73918365 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.936-585T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918365 | |||||||
| chr11:73918424 | G | A | 220 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0003g0006 others(217): Show |
240 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.936-526G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918424 | |||||||
| chr11:73918485 | A | AT | 7 | a0003c0003t0002g0266 a0003c0003t0002g0269 a0003c0003t0002g0285 others(4): Show |
7 | HG00639.hp1 HG01168.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.936-456dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 73918485 | ||||||
| chr11:73918762 | A | G | 2 | a0001c0001t0040g0299 a0001c0008t0039g0263 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.936-188A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918762 | |||||||
| chr11:73918807 | C | G | 1 | a0001c0001t0003g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.936-143C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 9/11 | chr11 | 73918807 | |||||||
| chr11:73919061 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1018+29G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919061 | |||||||
| chr11:73919292 | T | C | 109 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(106): Show |
117 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.1018+260T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919292 | |||||||
| chr11:73919321 | C | T | 3 | a0001c0001t0002g0337 a0001c0001t0015g0081 a0001c0001t0015g0083 |
3 | HG01358.hp1 HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1018+289C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919321 | |||||||
| chr11:73919346 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1018+314G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919346 | |||||||
| chr11:73919440 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1018+408C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919440 | |||||||
| chr11:73919542 | G | A | 1 | a0001c0001t0040g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1018+510G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919542 | |||||||
| chr11:73919574 | A | G | 1 | a0002c0002t0002g0056 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1018+542A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919574 | |||||||
| chr11:73919614 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1018+582A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919614 | |||||||
| chr11:73919840 | T | C | 1 | a0001c0001t0002g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1018+808T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919840 | |||||||
| chr11:73919884 | G | T | 133 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(130): Show |
141 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1018+852G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73919884 | |||||||
| chr11:73920008 | T | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1018+976T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920008 | |||||||
| chr11:73920029 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1018+997A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920029 | |||||||
| chr11:73920105 | G | A | 11 | a0001c0001t0008g0313 a0001c0001t0008g0315 a0001c0001t0008g0316 others(8): Show |
11 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1018+1073G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920105 | |||||||
| chr11:73920227 | A | T | 163 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0003g0006 others(160): Show |
182 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1018+1195A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920227 | |||||||
| chr11:73920282 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018+1250C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920282 | |||||||
| chr11:73920305 | G | A | 2 | a0001c0001t0022g0261 a0001c0001t0022g0262 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1018+1273G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920305 | |||||||
| chr11:73920454 | C | T | 2 | a0001c0001t0004g0096 a0001c0001t0004g0103 |
2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1018+1422C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920454 | |||||||
| chr11:73920523 | C | T | 24 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(21): Show |
24 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1018+1491C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920523 | |||||||
| chr11:73920573 | CTG | C | 11 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(8): Show |
12 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018+1542_1018+154 others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73920573 | |||||||
| chr11:73920851 | CA | C | 8 | a0001c0001t0004g0089 a0001c0001t0007g0036 a0001c0001t0008g0321 others(5): Show |
8 | HG01169.hp2 HG01496.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018+1834delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73920851 | ||||||
| chr11:73921072 | G | C | 1 | a0001c0001t0027g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1018+2040G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921072 | |||||||
| chr11:73921164 | G | A | 1 | a0003c0003t0032g0302 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1018+2132G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921164 | |||||||
| chr11:73921190 | C | T | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1018+2158C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921190 | |||||||
| chr11:73921299 | C | CA | 8 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0179 others(5): Show |
8 | HG02135.hp1 HG02300.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018+2282dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73921299 | ||||||
| chr11:73921299 | CA | C | 175 | a0001c0001t0002g0027 a0001c0001t0002g0337 a0001c0001t0004g0012 others(172): Show |
189 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.1018+2282delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73921299 | ||||||
| chr11:73921359 | G | A | 1 | a0001c0001t0004g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1018+2327G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921359 | |||||||
| chr11:73921393 | C | CT | 55 | a0001c0001t0044g0241 a0002c0002t0002g0003 a0002c0002t0002g0004 others(52): Show |
60 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1018+2372dupT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73921393 | ||||||
| chr11:73921393 | CT | C | 27 | a0001c0001t0001g0163 a0001c0001t0006g0310 a0001c0001t0006g0318 others(24): Show |
27 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1018+2372delT | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73921393 | ||||||
| chr11:73921505 | C | G | 2 | a0001c0001t0007g0034 a0001c0001t0007g0035 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1018+2473C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921505 | |||||||
| chr11:73921507 | C | A | 1 | a0001c0001t0044g0241 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1018+2475C>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921507 | |||||||
| chr11:73921508 | A | C | 1 | a0001c0001t0044g0241 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1018+2476A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921508 | |||||||
| chr11:73921546 | T | C | 2 | a0001c0001t0007g0034 a0001c0001t0007g0035 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1018+2514T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921546 | |||||||
| chr11:73921649 | G | A | 24 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0006g0319 others(21): Show |
24 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1018+2617G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921649 | |||||||
| chr11:73921744 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1018+2712G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921744 | |||||||
| chr11:73921908 | T | C | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1019-2707T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73921908 | |||||||
| chr11:73922019 | A | C | 11 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(8): Show |
12 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1019-2596A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922019 | |||||||
| chr11:73922053 | T | C | 2 | a0001c0001t0040g0299 a0001c0008t0039g0263 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1019-2562T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922053 | |||||||
| chr11:73922194 | T | C | 1 | a0001c0001t0044g0241 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1019-2421T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922194 | |||||||
| chr11:73922196 | G | T | 1 | a0001c0001t0044g0241 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1019-2419G>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922196 | |||||||
| chr11:73922201 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1019-2414C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922201 | |||||||
| chr11:73922202 | GC | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0128 others(2): Show |
5 | NA18950.hp1 NA18954.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1019-2410delC | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73922202 | ||||||
| chr11:73922205 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1019-2410C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922205 | |||||||
| chr11:73922264 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1019-2351G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922264 | |||||||
| chr11:73922445 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1019-2170C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922445 | |||||||
| chr11:73922577 | G | A | 38 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0018 others(35): Show |
44 | HG00544.hp2 HG00642.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1019-2038G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922577 | |||||||
| chr11:73922602 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1019-2013G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922602 | |||||||
| chr11:73922632 | A | G | 5 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0128 others(2): Show |
5 | NA18950.hp1 NA18954.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1019-1983A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922632 | |||||||
| chr11:73922645 | G | A | 3 | a0002c0002t0002g0306 a0002c0002t0002g0307 a0002c0002t0002g0308 |
3 | HG01496.hp1 HG02148.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1019-1970G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922645 | |||||||
| chr11:73922695 | T | G | 2 | a0001c0001t0006g0327 a0001c0001t0006g0332 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1019-1920T>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922695 | |||||||
| chr11:73922734 | G | A | 46 | a0001c0001t0002g0027 a0001c0001t0030g0028 a0003c0003t0002g0008 others(43): Show |
52 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1019-1881G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922734 | |||||||
| chr11:73922816 | C | CA | 85 | a0001c0001t0001g0149 a0001c0001t0003g0220 a0001c0001t0003g0221 others(82): Show |
91 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1019-1780dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73922816 | ||||||
| chr11:73922816 | C | CAA | 6 | a0001c0001t0022g0261 a0001c0001t0022g0262 a0002c0002t0002g0045 others(3): Show |
6 | HG02040.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1019-1781_1019-178 others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73922816 | ||||||
| chr11:73922816 | CA | C | 9 | a0001c0001t0001g0190 a0001c0001t0001g0201 a0001c0001t0003g0225 others(6): Show |
9 | HG01070.hp2 HG01169.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1019-1780delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73922816 | ||||||
| chr11:73922901 | G | A | 36 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(33): Show |
38 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1019-1714G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73922901 | |||||||
| chr11:73923022 | A | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1019-1593A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923022 | |||||||
| chr11:73923058 | A | G | 2 | a0001c0001t0008g0315 a0001c0001t0008g0322 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1019-1557A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923058 | |||||||
| chr11:73923097 | G | A | 2 | a0001c0001t0007g0034 a0001c0001t0007g0035 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1019-1518G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923097 | |||||||
| chr11:73923178 | A | C | 4 | a0001c0001t0006g0327 a0001c0001t0006g0329 a0001c0001t0006g0330 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-1437A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923178 | |||||||
| chr11:73923255 | T | C | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1019-1360T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923255 | |||||||
| chr11:73923382 | T | C | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1019-1233T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923382 | |||||||
| chr11:73923399 | A | C | 1 | a0001c0001t0044g0241 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1019-1216A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923399 | |||||||
| chr11:73923417 | G | A | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1019-1198G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923417 | |||||||
| chr11:73923679 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1019-936G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73923679 | |||||||
| chr11:73924004 | T | A | 1 | a0001c0001t0044g0241 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1019-611T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73924004 | |||||||
| chr11:73924004 | T | TAC | 24 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0218 others(21): Show |
24 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1019-588_1019-587d others(4): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73924004 | ||||||
| chr11:73924004 | T | TACAC | 13 | a0001c0001t0006g0319 a0001c0001t0006g0320 a0001c0001t0006g0325 others(10): Show |
14 | HG01106.hp1 HG02559.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1019-590_1019-587d others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73924004 | ||||||
| chr11:73924004 | T | TACACAC | 64 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0001c0001t0008g0313 others(61): Show |
69 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1019-592_1019-587d others(8): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73924004 | ||||||
| chr11:73924004 | T | TACACACA others(1): Show |
3 | a0001c0001t0008g0316 a0002c0002t0002g0045 a0002c0002t0002g0062 |
3 | HG02109.hp1 NA18985.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1019-594_1019-587d others(10): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73924004 | ||||||
| chr11:73924004 | T | TACACACA others(3): Show |
2 | a0001c0001t0040g0299 a0001c0008t0039g0263 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1019-596_1019-587d others(12): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 73924004 | ||||||
| chr11:73924174 | G | A | 1 | a0003c0003t0029g0275 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1019-441G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73924174 | |||||||
| chr11:73924193 | G | A | 1 | a0001c0001t0014g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1019-422G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73924193 | |||||||
| chr11:73924207 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1019-408C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73924207 | |||||||
| chr11:73924270 | C | T | 1 | a0001c0001t0004g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1019-345C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73924270 | |||||||
| chr11:73924485 | A | G | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1019-130A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 10/11 | chr11 | 73924485 | |||||||
| chr11:73924800 | A | T | 1 | a0001c0001t0044g0241 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1101+103A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73924800 | |||||||
| chr11:73924837 | A | C | 1 | a0001c0001t0001g0138 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1101+140A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73924837 | |||||||
| chr11:73924847 | A | G | 12 | a0001c0001t0008g0313 a0001c0001t0008g0315 a0001c0001t0008g0316 others(9): Show |
12 | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1101+150A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73924847 | |||||||
| chr11:73924909 | T | C | 2 | a0001c0001t0016g0328 a0001c0001t0016g0333 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1101+212T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73924909 | |||||||
| chr11:73924918 | C | T | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1101+221C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73924918 | |||||||
| chr11:73924988 | A | G | 11 | a0001c0001t0007g0009 a0001c0001t0007g0034 a0001c0001t0007g0035 others(8): Show |
12 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1101+291A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73924988 | |||||||
| chr11:73924991 | A | G | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1101+294A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73924991 | |||||||
| chr11:73925046 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1101+349T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73925046 | |||||||
| chr11:73925156 | C | CA | 13 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0001g0159 others(10): Show |
13 | HG00423.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1101+478dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 73925156 | ||||||
| chr11:73925156 | CA | C | 33 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(30): Show |
34 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1101+478delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 73925156 | ||||||
| chr11:73925168 | A | C | 45 | a0001c0001t0002g0027 a0001c0001t0030g0028 a0003c0003t0002g0008 others(42): Show |
51 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1101+471A>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73925168 | |||||||
| chr11:73925175 | AC | A | 4 | a0001c0001t0013g0257 a0001c0001t0013g0259 a0001c0001t0013g0260 others(1): Show |
4 | HG01106.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101+479delC | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73925175 | |||||||
| chr11:73925275 | G | C | 1 | a0001c0001t0003g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1101+578G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73925275 | |||||||
| chr11:73925286 | C | G | 5 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1101+589C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73925286 | |||||||
| chr11:73925462 | T | A | 5 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0012g0040 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1101+765T>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73925462 | |||||||
| chr11:73925465 | C | CA | 29 | a0001c0001t0003g0224 a0001c0001t0005g0135 a0001c0001t0005g0136 others(26): Show |
29 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1101+785dupA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 73925465 | ||||||
| chr11:73925465 | CA | C | 6 | a0001c0001t0003g0243 a0001c0001t0005g0132 a0001c0001t0022g0262 others(3): Show |
6 | HG02145.hp2 HG03209.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+785delA | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 73925465 | ||||||
| chr11:73925946 | A | G | 1 | a0001c0001t0005g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1101+1249A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73925946 | |||||||
| chr11:73926020 | ATCTC | A | 55 | a0001c0001t0006g0310 a0001c0001t0006g0318 a0002c0002t0002g0003 others(52): Show |
60 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1102-1263_1102-126 others(8): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 73926020 | ||||||
| chr11:73926058 | A | G | 3 | a0001c0001t0012g0040 a0001c0001t0012g0078 a0001c0001t0012g0082 |
3 | HG01884.hp1 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1102-1227A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926058 | |||||||
| chr11:73926111 | CTT | C | 46 | a0001c0001t0002g0027 a0001c0001t0030g0028 a0003c0003t0002g0008 others(43): Show |
52 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1102-1172_1102-117 others(6): Show |
PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 73926111 | ||||||
| chr11:73926115 | C | T | 102 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(99): Show |
109 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1102-1170C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926115 | |||||||
| chr11:73926119 | T | C | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1102-1166T>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926119 | |||||||
| chr11:73926138 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1102-1147C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926138 | |||||||
| chr11:73926167 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1102-1118C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926167 | |||||||
| chr11:73926169 | C | T | 2 | a0001c0001t0015g0081 a0001c0001t0015g0083 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1102-1116C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926169 | |||||||
| chr11:73926350 | A | G | 109 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(106): Show |
117 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.1102-935A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926350 | |||||||
| chr11:73926413 | A | T | 2 | a0001c0001t0014g0011 a0001c0001t0014g0085 |
3 | HG01884.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1102-872A>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926413 | |||||||
| chr11:73926425 | G | A | 1 | a0002c0002t0002g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1102-860G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926425 | |||||||
| chr11:73926514 | C | T | 3 | a0003c0003t0002g0022 a0003c0003t0002g0290 a0003c0003t0029g0275 |
4 | HG02683.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1102-771C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926514 | |||||||
| chr11:73926523 | C | G | 1 | a0002c0002t0002g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1102-762C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926523 | |||||||
| chr11:73926631 | C | G | 2 | a0001c0001t0006g0310 a0001c0001t0006g0318 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1102-654C>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926631 | |||||||
| chr11:73926634 | G | A | 1 | a0003c0003t0002g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1102-651G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926634 | |||||||
| chr11:73926696 | A | G | 137 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(134): Show |
145 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.1102-589A>G | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926696 | |||||||
| chr11:73926752 | G | C | 1 | a0001c0004t0001g0175 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1102-533G>C | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926752 | |||||||
| chr11:73926800 | G | A | 4 | a0001c0001t0014g0011 a0001c0001t0014g0085 a0001c0001t0022g0261 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102-485G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73926800 | |||||||
| chr11:73927043 | C | T | 3 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 |
3 | HG02622.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1102-242C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73927043 | |||||||
| chr11:73927142 | C | T | 32 | a0001c0001t0004g0012 a0001c0001t0004g0089 a0001c0001t0004g0090 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1102-143C>T | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73927142 | |||||||
| chr11:73927197 | G | A | 1 | a0001c0001t0009g0088 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1102-88G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73927197 | |||||||
| chr11:73927261 | G | A | 133 | a0001c0001t0002g0337 a0001c0001t0004g0012 a0001c0001t0004g0089 others(130): Show |
141 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1102-24G>A | PAAF1 | ENSG00000175575.13 | transcript | ENST00000310571.8 | protein_coding | 11/11 | chr11 | 73927261 |