Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2191 |
| ensemblid | ENSG00000078098.15 |
| hgncid | 3590 |
| symbol | FAP |
| name | fibroblast activation protein alpha |
| refseq_nuc | NM_004460.5 |
| refseq_prot | NP_004451.2 |
| ensembl_nuc | ENST00000188790.9 |
| ensembl_prot | ENSP00000188790.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 162170684 |
| end | 162243445 |
| strand | - |
| ver | v1.2 |
| region | chr2:162170684-162243445 |
| region5000 | chr2:162165684-162248445 |
| regionname0 | FAP_chr2_162170684_162243445 |
| regionname5000 | FAP_chr2_162165684_162248445 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 760 | 228 | 68 | 50 | 82 | 8 | 18 | 66 | FAP_chr2_162165684_162248445 | FAP | MKTWV others(755): Show |
chr2 | 162165684 | 162248445 |
| a0002 | 0/0 | 760 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | MKTWV others(755): Show |
chr2 | 162165684 | 162248445 |
| a0003 | 0/0 | 760 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | MKTWV others(755): Show |
chr2 | 162165684 | 162248445 |
| a0004 | 0/0 | 760 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | MKTWV others(755): Show |
chr2 | 162165684 | 162248445 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2280 | 182 | 63 | 34 | 59 | 7 | 17 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 | ||
| a0001c0002 | 0/0 | 2280 | 36 | 0 | 14 | 21 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 | ||
| a0001c0003 | 0/0 | 2280 | 5 | 5 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 | ||
| a0001c0004 | 0/0 | 2280 | 3 | 0 | 0 | 2 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 | ||
| a0001c0007 | 0/0 | 2280 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 | ||
| a0002c0005 | 0/0 | 2280 | 3 | 3 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 | ||
| a0003c0006 | 0/0 | 2280 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 | ||
| a0004c0008 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | ATGAA others(2275): Show |
chr2 | 162165684 | 162248445 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2696 | 179 | 60 | 34 | 59 | 7 | 17 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0001c0001t0002 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0001c0001t0003 | 0/0 | 2696 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0001c0002t0001 | 0/0 | 2696 | 36 | 0 | 14 | 21 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0001c0003t0001 | 0/0 | 2696 | 5 | 5 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0001c0004t0001 | 0/0 | 2696 | 3 | 0 | 0 | 2 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0001c0007t0001 | 0/0 | 2696 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0002c0005t0001 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0002c0005t0002 | 0/0 | 2696 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0003c0006t0001 | 0/0 | 2696 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| a0004c0008t0001 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | GTCCT others(2691): Show |
chr2 | 162165684 | 162248445 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0004t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0007t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0001c0007t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0002c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0002c0005t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0002c0005t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0003c0006t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0003c0006t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| a0004c0008t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01257 | hp2 | a0001 | c0007 | t0001 | g0056 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01258 | hp1 | a0001 | c0007 | t0001 | g0057 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02280 | hp1 | a0002 | c0005 | t0001 | g0065 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0080 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02630 | hp2 | a0003 | c0006 | t0001 | g0190 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0082 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03139 | hp2 | a0004 | c0008 | t0001 | g0021 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03209 | hp1 | a0002 | c0005 | t0002 | g0210 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03486 | hp2 | a0002 | c0005 | t0002 | g0209 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19085 | hp1 | a0001 | c0004 | t0001 | g0012 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ASW | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0093 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02559 | hp1 | a0003 | c0006 | t0001 | g0085 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | ACB | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | LWK | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0188 | REF | REF | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0124 | REF | REF | FAP_chr2_162165684_162248445 | FAP | chr2 | 162165684 | 162248445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:162218062 | G | A | 1 | a0004 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.686C>T | p.Thr229Met | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/26 | 804/2696 | 686/2283 | 229/760 | chr2 | 162218062 | |||
| chr2:162218114 | G | A | 1 | a0002 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.634C>T | p.Leu212Phe | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/26 | 752/2696 | 634/2283 | 212/760 | chr2 | 162218114 | |||
| chr2:162225536 | G | T | 1 | a0003 | 2 | HG02559.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.232C>A | p.Leu78Ile | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/26 | 350/2696 | 232/2283 | 78/760 | chr2 | 162225536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:162171060 | G | A | 1 | a0001c0007 | 2 | HG01257.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.2202C>T | p.His734His | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 26/26 | 2320/2696 | 2202/2283 | 734/760 | chr2 | 162171060 | |||
| chr2:162173786 | C | T | 1 | a0001c0004 | 3 | NA18952.hp2 NA19085.hp1 NA20805.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1971G>A | p.Ala657Ala | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 23/26 | 2089/2696 | 1971/2283 | 657/760 | chr2 | 162173786 | |||
| chr2:162198785 | G | A | 1 | a0002c0005 | 3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.1374C>T | p.Tyr458Tyr | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/26 | 1492/2696 | 1374/2283 | 458/760 | chr2 | 162198785 | |||
| chr2:162219085 | T | G | 1 | a0001c0003 | 5 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.585A>C | p.Gly195Gly | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/26 | 703/2696 | 585/2283 | 195/760 | chr2 | 162219085 | |||
| chr2:162224472 | A | G | 1 | a0001c0002 | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
synonymous_variant | LOW | c.354T>C | p.Tyr118Tyr | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 5/26 | 472/2696 | 354/2283 | 118/760 | chr2 | 162224472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:162243397 | G | A | 2 | a0001c0001t0002 a0002c0005t0002 |
3 | HG03209.hp1 HG03486.hp2 NA21309.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 1/26 | chr2 | 162243397 | |||||||
| chr2:162243414 | C | A | 1 | a0001c0001t0003 | 2 | HG02970.hp2 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-87G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 1/26 | 87 | chr2 | 162243414 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:162171308 | G | A | 23 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(20): Show |
25 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.2182-228C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171308 | |||||||
| chr2:162171809 | CT | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(56): Show |
68 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2182-730delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171809 | |||||||
| chr2:162171813 | T | A | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2182-733A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171813 | |||||||
| chr2:162171935 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0090 others(1): Show |
4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2182-855A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171935 | |||||||
| chr2:162171980 | T | C | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.2181+831A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162171980 | |||||||
| chr2:162172174 | A | C | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2181+637T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162172174 | |||||||
| chr2:162172378 | A | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(65): Show |
77 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.2181+433T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 25/25 | chr2 | 162172378 | |||||||
| chr2:162173644 | T | A | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2034+79A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 23/25 | chr2 | 162173644 | |||||||
| chr2:162173826 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0063 others(28): Show |
32 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1970-39A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162173826 | |||||||
| chr2:162174025 | A | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0126 |
3 | HG02071.hp1 HG02083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1970-238T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174025 | |||||||
| chr2:162174200 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0141 others(5): Show |
8 | HG02155.hp2 HG02273.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1970-413G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174200 | |||||||
| chr2:162174494 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(14): Show |
22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1969+373C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174494 | |||||||
| chr2:162174527 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1969+340C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174527 | |||||||
| chr2:162174834 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1969+33G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 22/25 | chr2 | 162174834 | |||||||
| chr2:162175519 | T | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(205): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1870-553A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175519 | |||||||
| chr2:162175548 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1870-582C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175548 | |||||||
| chr2:162175578 | T | C | 2 | a0003c0006t0001g0085 a0003c0006t0001g0190 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1870-612A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175578 | |||||||
| chr2:162175824 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(56): Show |
68 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1870-858G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162175824 | |||||||
| chr2:162176261 | T | G | 1 | a0001c0001t0001g0145 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1870-1295A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162176261 | |||||||
| chr2:162177039 | TGAA | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0141 others(5): Show |
8 | HG02155.hp2 HG02273.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1870-2076_1870-207 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177039 | |||||||
| chr2:162177067 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1870-2101A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177067 | |||||||
| chr2:162177611 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1870-2645A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177611 | |||||||
| chr2:162177643 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(14): Show |
22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1870-2677G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177643 | |||||||
| chr2:162177951 | T | C | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1870-2985A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162177951 | |||||||
| chr2:162178060 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1870-3094G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178060 | |||||||
| chr2:162178479 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
6 | HG00558.hp2 HG00609.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-3513C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178479 | |||||||
| chr2:162178497 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1870-3531G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178497 | |||||||
| chr2:162178581 | G | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0139 a0001c0001t0001g0199 |
3 | HG02922.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1870-3615C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178581 | |||||||
| chr2:162178698 | TC | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0204 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1870-3733delG | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162178698 | |||||||
| chr2:162179245 | G | GT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0115 others(2): Show |
5 | HG00741.hp2 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1869+4168dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179245 | |||||||
| chr2:162179245 | GT | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
172 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1869+4168delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179245 | |||||||
| chr2:162179245 | GTT | G | 25 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(22): Show |
27 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1869+4167_1869+416 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179245 | |||||||
| chr2:162179277 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG02155.hp2 NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1869+4137T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179277 | |||||||
| chr2:162179431 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+3983G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179431 | |||||||
| chr2:162179466 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(6): Show |
14 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1869+3948T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179466 | |||||||
| chr2:162179708 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0202 a0001c0001t0003g0212 |
3 | HG02451.hp2 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1869+3706T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179708 | |||||||
| chr2:162179759 | G | GATCT | 4 | a0001c0001t0001g0178 a0001c0003t0001g0080 a0002c0005t0002g0209 others(1): Show |
4 | HG01168.hp1 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3651_1869+365 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179759 | |||||||
| chr2:162179759 | G | GATCTATC others(1): Show |
4 | a0001c0001t0001g0106 a0001c0001t0001g0207 a0001c0001t0003g0211 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3647_1869+365 others(12): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179759 | |||||||
| chr2:162179759 | G | GATCTATC others(5): Show |
3 | a0001c0001t0001g0193 a0001c0003t0001g0081 a0001c0003t0001g0082 |
3 | HG02630.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1869+3643_1869+365 others(16): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179759 | |||||||
| chr2:162179779 | T | TATC | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1869+3632_1869+363 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179779 | |||||||
| chr2:162179782 | CTATCTAT others(5): Show |
C | 1 | a0001c0001t0002g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+3620_1869+363 others(16): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179782 | |||||||
| chr2:162179786 | CTATCTA | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0076 |
2 | HG02451.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1869+3622_1869+362 others(10): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179786 | |||||||
| chr2:162179787 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1869+3627A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179787 | |||||||
| chr2:162179787 | T | TATCA | 2 | a0001c0001t0001g0002 a0001c0001t0001g0159 |
2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1869+3626_1869+362 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179787 | |||||||
| chr2:162179788 | ATC | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0168 |
2 | NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1869+3624_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179788 | |||||||
| chr2:162179790 | C | CAA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(19): Show |
27 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3623_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179790 | |||||||
| chr2:162179790 | CTA | C | 67 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(64): Show |
71 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1869+3622_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179790 | |||||||
| chr2:162179791 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1869+3623A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179791 | |||||||
| chr2:162179792 | A | ATC | 8 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0099 others(5): Show |
9 | HG01258.hp2 HG01346.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1869+3621_1869+362 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | |||||||
| chr2:162179792 | A | ATCTATC | 11 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0114 others(8): Show |
13 | HG00735.hp2 HG01891.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1869+3621_1869+362 others(10): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | |||||||
| chr2:162179792 | A | ATCTATCT others(3): Show |
4 | a0001c0001t0001g0024 a0001c0001t0001g0096 a0001c0001t0001g0185 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+3621_1869+362 others(14): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | |||||||
| chr2:162179792 | A | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(19): Show |
27 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3622T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179792 | |||||||
| chr2:162179794 | A | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(76): Show |
87 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1869+3620T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179794 | |||||||
| chr2:162179796 | A | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(8): Show |
14 | HG00639.hp1 HG00735.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1869+3618T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179796 | |||||||
| chr2:162179798 | A | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0067 others(19): Show |
27 | HG00639.hp2 HG01106.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3616T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179798 | |||||||
| chr2:162179800 | A | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0011 |
4 | HG00735.hp2 HG01258.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3614T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179800 | |||||||
| chr2:162179800 | ATATATAT others(6): Show |
A | 1 | a0001c0002t0001g0025 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1869+3601_1869+361 others(17): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179800 | |||||||
| chr2:162179802 | A | C | 3 | a0001c0001t0001g0022 a0001c0002t0001g0048 a0001c0002t0001g0052 |
3 | HG02258.hp1 NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1869+3612T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179802 | |||||||
| chr2:162179804 | ATATATAT others(2): Show |
A | 25 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0098 others(22): Show |
27 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1869+3601_1869+360 others(13): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179804 | |||||||
| chr2:162179808 | A | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0002c0005t0001g0065 |
3 | HG02280.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1869+3606T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179808 | |||||||
| chr2:162179808 | ATATAT | A | 8 | a0001c0001t0001g0087 a0001c0002t0001g0004 a0001c0002t0001g0031 others(5): Show |
9 | HG01175.hp1 HG02004.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.1869+3601_1869+360 others(9): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179808 | |||||||
| chr2:162179809 | TA | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1869+3604delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179809 | |||||||
| chr2:162179809 | TATA | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0118 others(1): Show |
4 | HG02602.hp1 HG03490.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1869+3602_1869+360 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179809 | |||||||
| chr2:162179810 | A | ATTTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0067 others(3): Show |
9 | HG01106.hp1 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1869+3603_1869+360 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179810 | |||||||
| chr2:162179810 | A | ATTTTTTT others(40): Show |
1 | a0001c0001t0001g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1869+3603_1869+360 others(51): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179810 | |||||||
| chr2:162179810 | A | T | 11 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0069 others(8): Show |
11 | HG02258.hp2 HG02280.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1869+3604T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179810 | |||||||
| chr2:162179812 | A | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
60 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1869+3602T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179812 | |||||||
| chr2:162179813 | T | TA | 7 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0160 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869+3600_1869+360 others(5): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179813 | |||||||
| chr2:162179813 | T | TATA | 2 | a0001c0001t0001g0165 a0001c0001t0001g0183 |
2 | HG00733.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1869+3600_1869+360 others(7): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179813 | |||||||
| chr2:162179814 | T | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0117 a0001c0001t0001g0159 others(3): Show |
7 | HG00733.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1869+3600A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179814 | |||||||
| chr2:162179816 | T | A | 4 | a0001c0001t0001g0015 a0001c0001t0003g0212 a0002c0005t0002g0209 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+3598A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179816 | |||||||
| chr2:162179839 | C | T | 2 | a0001c0001t0001g0109 a0001c0002t0001g0049 |
2 | HG00140.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1869+3575G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179839 | |||||||
| chr2:162179869 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(60): Show |
72 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1869+3545A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162179869 | |||||||
| chr2:162180028 | C | T | 10 | a0001c0001t0001g0179 a0001c0002t0001g0003 a0001c0002t0001g0028 others(7): Show |
11 | HG01069.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1869+3386G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180028 | |||||||
| chr2:162180092 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1869+3322C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180092 | |||||||
| chr2:162180107 | A | G | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1869+3307T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180107 | |||||||
| chr2:162180309 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1869+3105T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180309 | |||||||
| chr2:162180350 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1869+3064G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180350 | |||||||
| chr2:162180830 | T | A | 1 | a0001c0002t0001g0048 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1869+2584A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162180830 | |||||||
| chr2:162181044 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1869+2370C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181044 | |||||||
| chr2:162181170 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(60): Show |
72 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1869+2244T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181170 | |||||||
| chr2:162181255 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1869+2159G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181255 | |||||||
| chr2:162181392 | C | G | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1869+2022G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181392 | |||||||
| chr2:162181416 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(14): Show |
22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1869+1998T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181416 | |||||||
| chr2:162181517 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1869+1897A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181517 | |||||||
| chr2:162181872 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0149 |
3 | NA18992.hp1 NA18994.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1869+1542C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181872 | |||||||
| chr2:162181915 | T | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0076 a0001c0001t0001g0088 others(16): Show |
21 | HG02074.hp2 HG02083.hp2 HG03017.hp1 others(18): Show |
intron_variant | MODIFIER | c.1869+1499A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162181915 | |||||||
| chr2:162182113 | G | C | 1 | a0001c0001t0002g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1869+1301C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162182113 | |||||||
| chr2:162182309 | C | T | 2 | a0001c0002t0001g0028 a0001c0002t0001g0042 |
2 | HG01175.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1869+1105G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162182309 | |||||||
| chr2:162183091 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1869+323T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162183091 | |||||||
| chr2:162183256 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1869+158G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 21/25 | chr2 | 162183256 | |||||||
| chr2:162183576 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1815-108G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183576 | |||||||
| chr2:162183644 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1815-176C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183644 | |||||||
| chr2:162183730 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1815-262G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183730 | |||||||
| chr2:162183731 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0003g0211 |
3 | HG02970.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1815-263C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183731 | |||||||
| chr2:162183771 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1815-303A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162183771 | |||||||
| chr2:162184248 | G | A | 2 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1815-780C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184248 | |||||||
| chr2:162184515 | A | T | 1 | a0001c0002t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1815-1047T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184515 | |||||||
| chr2:162184772 | TA | T | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1815-1305delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184772 | |||||||
| chr2:162184877 | T | G | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1815-1409A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184877 | |||||||
| chr2:162184894 | A | G | 13 | a0001c0001t0001g0106 a0001c0001t0001g0175 a0001c0001t0001g0176 others(10): Show |
13 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1815-1426T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162184894 | |||||||
| chr2:162185074 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0003g0212 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1815-1606G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185074 | |||||||
| chr2:162185171 | A | G | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1815-1703T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185171 | |||||||
| chr2:162185301 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1815-1833A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185301 | |||||||
| chr2:162185313 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0168 a0001c0001t0001g0206 |
3 | NA19004.hp2 NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1815-1845G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185313 | |||||||
| chr2:162185510 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0003g0212 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1815-2042C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185510 | |||||||
| chr2:162185977 | C | T | 1 | a0004c0008t0001g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1814+2192G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162185977 | |||||||
| chr2:162186131 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0003g0212 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1814+2038A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186131 | |||||||
| chr2:162186410 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0203 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1814+1759A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186410 | |||||||
| chr2:162186426 | A | G | 1 | a0001c0002t0001g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1814+1743T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186426 | |||||||
| chr2:162186585 | C | T | 1 | a0001c0002t0001g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1814+1584G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186585 | |||||||
| chr2:162186651 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1814+1518C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186651 | |||||||
| chr2:162186712 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1814+1457G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186712 | |||||||
| chr2:162186775 | C | T | 5 | a0001c0002t0001g0004 a0001c0002t0001g0044 a0001c0002t0001g0048 others(2): Show |
6 | NA18975.hp2 NA19004.hp1 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.1814+1394G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186775 | |||||||
| chr2:162186818 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1814+1351C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186818 | |||||||
| chr2:162186831 | T | TA | 2 | a0001c0001t0001g0015 a0001c0001t0001g0163 |
3 | HG02896.hp2 HG02897.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1814+1337_1814+133 others(5): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186831 | |||||||
| chr2:162186842 | C | CACTCCTA others(5): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0163 |
3 | HG02896.hp2 HG02897.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1814+1326_1814+132 others(16): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162186842 | |||||||
| chr2:162187169 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1814+1000G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187169 | |||||||
| chr2:162187218 | C | A | 1 | a0001c0001t0001g0201 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1814+951G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187218 | |||||||
| chr2:162187243 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1814+926C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187243 | |||||||
| chr2:162187357 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1814+812T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187357 | |||||||
| chr2:162187360 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1814+809G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187360 | |||||||
| chr2:162187511 | G | T | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1814+658C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187511 | |||||||
| chr2:162187561 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0003g0212 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1814+608C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187561 | |||||||
| chr2:162187641 | C | A | 2 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1814+528G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187641 | |||||||
| chr2:162187709 | A | T | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1814+460T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187709 | |||||||
| chr2:162187845 | G | A | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1814+324C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187845 | |||||||
| chr2:162187880 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0090 others(1): Show |
4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+289C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 20/25 | chr2 | 162187880 | |||||||
| chr2:162188384 | A | T | 1 | a0001c0001t0001g0017 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1620-21T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188384 | |||||||
| chr2:162188460 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1620-97A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188460 | |||||||
| chr2:162188769 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1619+334A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188769 | |||||||
| chr2:162188922 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1619+181T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188922 | |||||||
| chr2:162188948 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1619+155G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162188948 | |||||||
| chr2:162189002 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1619+101G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162189002 | |||||||
| chr2:162189052 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1619+51A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 19/25 | chr2 | 162189052 | |||||||
| chr2:162189181 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0003g0212 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1550-9T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189181 | |||||||
| chr2:162189323 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1550-151A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189323 | |||||||
| chr2:162189424 | C | T | 2 | a0001c0002t0001g0029 a0001c0002t0001g0030 |
2 | HG00621.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1549+232G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189424 | |||||||
| chr2:162189458 | A | T | 1 | a0001c0001t0002g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1549+198T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189458 | |||||||
| chr2:162189533 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+123A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189533 | |||||||
| chr2:162189534 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+122C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189534 | |||||||
| chr2:162189538 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+118A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189538 | |||||||
| chr2:162189539 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+117G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189539 | |||||||
| chr2:162189540 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+116G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189540 | |||||||
| chr2:162189541 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+115A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189541 | |||||||
| chr2:162189542 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+114C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189542 | |||||||
| chr2:162189543 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+113A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189543 | |||||||
| chr2:162189546 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+110A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189546 | |||||||
| chr2:162189548 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+108A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189548 | |||||||
| chr2:162189549 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+107A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189549 | |||||||
| chr2:162189553 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+103T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189553 | |||||||
| chr2:162189554 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+102C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189554 | |||||||
| chr2:162189556 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+100A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189556 | |||||||
| chr2:162189557 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+99G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189557 | |||||||
| chr2:162189558 | G | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0113 |
2 | HG02258.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1549+98C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189558 | |||||||
| chr2:162189559 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+97G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189559 | |||||||
| chr2:162189561 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+95C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189561 | |||||||
| chr2:162189564 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+92A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189564 | |||||||
| chr2:162189565 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+91A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189565 | |||||||
| chr2:162189566 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+90A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189566 | |||||||
| chr2:162189567 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+89C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189567 | |||||||
| chr2:162189568 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+88G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189568 | |||||||
| chr2:162189570 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+86G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189570 | |||||||
| chr2:162189571 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+85A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189571 | |||||||
| chr2:162189572 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+84C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189572 | |||||||
| chr2:162189573 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+83A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189573 | |||||||
| chr2:162189576 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+80G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189576 | |||||||
| chr2:162189580 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+76G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189580 | |||||||
| chr2:162189582 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+74G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189582 | |||||||
| chr2:162189584 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+72G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189584 | |||||||
| chr2:162189585 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+71A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189585 | |||||||
| chr2:162189587 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+69A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189587 | |||||||
| chr2:162189588 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+68C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189588 | |||||||
| chr2:162189589 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+67G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189589 | |||||||
| chr2:162189590 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+66A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189590 | |||||||
| chr2:162189591 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+65A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189591 | |||||||
| chr2:162189592 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+64A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189592 | |||||||
| chr2:162189593 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+63A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189593 | |||||||
| chr2:162189594 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+62A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189594 | |||||||
| chr2:162189595 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1549+61A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 18/25 | chr2 | 162189595 | |||||||
| chr2:162189798 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1451-44A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162189798 | |||||||
| chr2:162189837 | T | A | 2 | a0001c0001t0001g0202 a0001c0001t0003g0212 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1451-83A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162189837 | |||||||
| chr2:162190036 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0099 |
3 | HG01258.hp2 HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1451-282G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190036 | |||||||
| chr2:162190357 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1451-603C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190357 | |||||||
| chr2:162190395 | T | TAC | 4 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0084 others(1): Show |
4 | HG00741.hp2 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451-643_1451-642d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190395 | |||||||
| chr2:162190395 | TAC | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0170 a0001c0001t0003g0211 |
3 | HG01361.hp1 HG02602.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1451-643_1451-642d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190395 | |||||||
| chr2:162190527 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1451-773T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190527 | |||||||
| chr2:162190740 | T | C | 2 | a0001c0002t0001g0029 a0001c0002t0001g0030 |
2 | HG00621.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1451-986A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162190740 | |||||||
| chr2:162191073 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1451-1319C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191073 | |||||||
| chr2:162191329 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1451-1575C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191329 | |||||||
| chr2:162191331 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1451-1577T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191331 | |||||||
| chr2:162191375 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(16): Show |
25 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1451-1621G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191375 | |||||||
| chr2:162191438 | A | G | 23 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(20): Show |
25 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1451-1684T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191438 | |||||||
| chr2:162191542 | A | AGCACCTA others(7): Show |
1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1451-1802_1451-178 others(18): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191542 | |||||||
| chr2:162191624 | G | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0187 |
2 | HG02622.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1451-1870C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191624 | |||||||
| chr2:162191787 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1451-2033C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191787 | |||||||
| chr2:162191894 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(21): Show |
30 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1451-2140G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162191894 | |||||||
| chr2:162192461 | C | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0180 |
3 | HG01168.hp1 HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1450+2240G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192461 | |||||||
| chr2:162192496 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1450+2205G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192496 | |||||||
| chr2:162192508 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0090 others(1): Show |
4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+2193C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192508 | |||||||
| chr2:162192603 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1450+2098A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162192603 | |||||||
| chr2:162193129 | T | C | 39 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
42 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1450+1572A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193129 | |||||||
| chr2:162193166 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1450+1535C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193166 | |||||||
| chr2:162193242 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0182 |
2 | HG00558.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1450+1459G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193242 | |||||||
| chr2:162193289 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1450+1412T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193289 | |||||||
| chr2:162193397 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1450+1304C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193397 | |||||||
| chr2:162193400 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1450+1301C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193400 | |||||||
| chr2:162193498 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1450+1203T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193498 | |||||||
| chr2:162193693 | AC | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0144 |
3 | HG01358.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1450+1007delG | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193693 | |||||||
| chr2:162193964 | T | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(14): Show |
22 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1450+737A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193964 | |||||||
| chr2:162193988 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1450+713T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162193988 | |||||||
| chr2:162194153 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1450+548C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194153 | |||||||
| chr2:162194272 | C | CCA | 36 | a0001c0001t0001g0017 a0001c0001t0001g0058 a0001c0001t0001g0090 others(33): Show |
37 | HG00558.hp1 HG00621.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1450+427_1450+428d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194272 | |||||||
| chr2:162194272 | C | CCACA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(14): Show |
23 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1450+425_1450+428d others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194272 | |||||||
| chr2:162194272 | C | CCACACA | 5 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0193 others(2): Show |
6 | HG02258.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1450+423_1450+428d others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194272 | |||||||
| chr2:162194330 | AG | A | 15 | a0001c0001t0001g0179 a0001c0002t0001g0003 a0001c0002t0001g0026 others(12): Show |
16 | HG00738.hp1 HG01069.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1450+370delC | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194330 | |||||||
| chr2:162194332 | G | GA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0113 others(3): Show |
7 | HG00621.hp1 HG01258.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1450+368dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194332 | |||||||
| chr2:162194332 | GA | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(17): Show |
26 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1450+368delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194332 | |||||||
| chr2:162194349 | A | T | 1 | a0002c0005t0002g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1450+352T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194349 | |||||||
| chr2:162194541 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0090 others(1): Show |
4 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+160T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194541 | |||||||
| chr2:162194683 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0003g0212 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1450+18T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 17/25 | chr2 | 162194683 | |||||||
| chr2:162194792 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1403-44T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162194792 | |||||||
| chr2:162194905 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(206): Show |
231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1403-157G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162194905 | |||||||
| chr2:162195133 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1403-385T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195133 | |||||||
| chr2:162195194 | G | C | 23 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0087 others(20): Show |
25 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1403-446C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195194 | |||||||
| chr2:162195229 | A | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(5): Show |
13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1403-481T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195229 | |||||||
| chr2:162195230 | C | T | 2 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-482G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195230 | |||||||
| chr2:162195419 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1403-671T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195419 | |||||||
| chr2:162195429 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1403-681T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195429 | |||||||
| chr2:162195515 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0003g0211 |
3 | HG02970.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1403-767G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195515 | |||||||
| chr2:162195516 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(16): Show |
24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1403-768C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195516 | |||||||
| chr2:162195539 | G | A | 2 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-791C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195539 | |||||||
| chr2:162195615 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1403-867A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195615 | |||||||
| chr2:162195807 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0134 |
3 | NA18974.hp1 NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1403-1059A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195807 | |||||||
| chr2:162195811 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0204 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1403-1063A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195811 | |||||||
| chr2:162195864 | C | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0144 |
3 | HG01358.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1403-1116G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195864 | |||||||
| chr2:162195867 | C | G | 22 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0086 others(19): Show |
22 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1403-1119G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195867 | |||||||
| chr2:162195896 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1403-1148A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162195896 | |||||||
| chr2:162196302 | G | A | 2 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-1554C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196302 | |||||||
| chr2:162196362 | A | T | 1 | a0001c0001t0002g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1403-1614T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196362 | |||||||
| chr2:162196394 | T | C | 2 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1403-1646A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196394 | |||||||
| chr2:162196410 | C | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1403-1662G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196410 | |||||||
| chr2:162196518 | C | CT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
7 | HG02280.hp1 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403-1771dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196518 | |||||||
| chr2:162196518 | CT | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0084 others(37): Show |
44 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1403-1771delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196518 | |||||||
| chr2:162196521 | T | G | 1 | a0001c0002t0001g0051 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1403-1773A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196521 | |||||||
| chr2:162196599 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1403-1851C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196599 | |||||||
| chr2:162196660 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1403-1912G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196660 | |||||||
| chr2:162196664 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1403-1916T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162196664 | |||||||
| chr2:162197072 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1402+1685T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197072 | |||||||
| chr2:162197362 | T | C | 2 | a0003c0006t0001g0085 a0003c0006t0001g0190 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1402+1395A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197362 | |||||||
| chr2:162197373 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1402+1384A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197373 | |||||||
| chr2:162197789 | A | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0189 |
2 | HG00639.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1402+968T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197789 | |||||||
| chr2:162197855 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1402+902G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197855 | |||||||
| chr2:162197858 | A | G | 1 | a0001c0002t0001g0045 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1402+899T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162197858 | |||||||
| chr2:162198033 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1402+724A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198033 | |||||||
| chr2:162198104 | G | A | 18 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(15): Show |
20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.1402+653C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198104 | |||||||
| chr2:162198214 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(64): Show |
76 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.1402+543G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198214 | |||||||
| chr2:162198272 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1402+485G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198272 | |||||||
| chr2:162198286 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(16): Show |
24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1402+471C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198286 | |||||||
| chr2:162198415 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1402+342C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198415 | |||||||
| chr2:162198556 | ACT | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0186 |
2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1402+199_1402+200d others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198556 | |||||||
| chr2:162198558 | T | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1402+199A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198558 | |||||||
| chr2:162198684 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(5): Show |
13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1402+73C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 16/25 | chr2 | 162198684 | |||||||
| chr2:162199168 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1278-287G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199168 | |||||||
| chr2:162199222 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
10 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1278-341C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199222 | |||||||
| chr2:162199485 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1278-604A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199485 | |||||||
| chr2:162199552 | A | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1278-671T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199552 | |||||||
| chr2:162199570 | C | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(5): Show |
13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1278-689G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199570 | |||||||
| chr2:162199647 | C | T | 34 | a0001c0001t0001g0161 a0001c0002t0001g0003 a0001c0002t0001g0004 others(31): Show |
37 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.1278-766G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199647 | |||||||
| chr2:162199667 | CA | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(16): Show |
24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1278-787delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199667 | |||||||
| chr2:162199788 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1277+778G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199788 | |||||||
| chr2:162199803 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1277+763G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199803 | |||||||
| chr2:162199876 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0003g0212 |
3 | HG00140.hp1 HG00741.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1277+690C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199876 | |||||||
| chr2:162199877 | G | C | 1 | a0001c0001t0003g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1277+689C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199877 | |||||||
| chr2:162199906 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1277+660C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199906 | |||||||
| chr2:162199927 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1277+639T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199927 | |||||||
| chr2:162199933 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1277+633T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162199933 | |||||||
| chr2:162200155 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1277+411C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200155 | |||||||
| chr2:162200255 | T | A | 1 | a0001c0002t0001g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1277+311A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200255 | |||||||
| chr2:162200393 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(16): Show |
24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1277+173G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200393 | |||||||
| chr2:162200414 | T | TTATACTG others(6): Show |
52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(49): Show |
60 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1277+151_1277+152i others(15): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200414 | |||||||
| chr2:162200442 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(66): Show |
79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1277+124T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200442 | |||||||
| chr2:162200468 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0032 |
2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1277+98C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 15/25 | chr2 | 162200468 | |||||||
| chr2:162200801 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1224-182T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162200801 | |||||||
| chr2:162200857 | G | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1224-238C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162200857 | |||||||
| chr2:162201025 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1224-406C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201025 | |||||||
| chr2:162201071 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1224-452C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201071 | |||||||
| chr2:162201241 | AT | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1224-623delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201241 | |||||||
| chr2:162201278 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1224-659C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201278 | |||||||
| chr2:162201336 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1224-717T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201336 | |||||||
| chr2:162201383 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0159 a0001c0007t0001g0056 others(1): Show |
5 | HG00733.hp2 HG01175.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1224-764A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201383 | |||||||
| chr2:162201387 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1224-768T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201387 | |||||||
| chr2:162201493 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1224-874G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201493 | |||||||
| chr2:162201504 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1224-885A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201504 | |||||||
| chr2:162201638 | G | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0102 |
2 | NA18977.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1224-1019C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162201638 | |||||||
| chr2:162202016 | C | T | 3 | a0002c0005t0001g0065 a0002c0005t0002g0209 a0002c0005t0002g0210 |
3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1223+856G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202016 | |||||||
| chr2:162202070 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1223+802A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202070 | |||||||
| chr2:162202083 | A | T | 1 | a0001c0002t0001g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1223+789T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202083 | |||||||
| chr2:162202298 | A | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA18946.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1223+574T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202298 | |||||||
| chr2:162202314 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1223+558G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202314 | |||||||
| chr2:162202823 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1223+49C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 14/25 | chr2 | 162202823 | |||||||
| chr2:162202980 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1153-38G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 13/25 | chr2 | 162202980 | |||||||
| chr2:162203235 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1048-90T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203235 | |||||||
| chr2:162203295 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0151 |
2 | HG02155.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1048-150G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203295 | |||||||
| chr2:162203461 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
10 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048-316C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203461 | |||||||
| chr2:162203528 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1048-383A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203528 | |||||||
| chr2:162203717 | G | A | 3 | a0002c0005t0001g0065 a0002c0005t0002g0209 a0002c0005t0002g0210 |
3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1048-572C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162203717 | |||||||
| chr2:162204013 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1048-868T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204013 | |||||||
| chr2:162204017 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1048-872T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204017 | |||||||
| chr2:162204084 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1048-939A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204084 | |||||||
| chr2:162204457 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1048-1312C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204457 | |||||||
| chr2:162204552 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18946.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1048-1407C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204552 | |||||||
| chr2:162204620 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0090 a0001c0001t0001g0131 others(1): Show |
4 | HG03139.hp2 HG03453.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-1475C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204620 | |||||||
| chr2:162204914 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1048-1769A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204914 | |||||||
| chr2:162204934 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0138 |
3 | HG00735.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1048-1789G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162204934 | |||||||
| chr2:162205105 | A | G | 1 | a0001c0002t0001g0037 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1048-1960T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205105 | |||||||
| chr2:162205147 | T | G | 4 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | HG01168.hp1 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048-2002A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205147 | |||||||
| chr2:162205607 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0163 |
3 | HG02896.hp2 HG02897.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1048-2462C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205607 | |||||||
| chr2:162205790 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1048-2645C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205790 | |||||||
| chr2:162205813 | A | G | 1 | a0001c0001t0001g0007 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1048-2668T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162205813 | |||||||
| chr2:162206112 | T | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0203 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1048-2967A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206112 | |||||||
| chr2:162206368 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0004t0001g0012 |
4 | NA18946.hp2 NA18952.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-3223C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206368 | |||||||
| chr2:162206521 | A | AT | 45 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0084 others(42): Show |
49 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1048-3377dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206521 | |||||||
| chr2:162206592 | AATAATTG others(21): Show |
A | 1 | a0001c0002t0001g0046 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1047+3332_1047+335 others(32): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206592 | |||||||
| chr2:162206669 | T | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(66): Show |
79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1047+3283A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206669 | |||||||
| chr2:162206710 | C | A | 18 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(15): Show |
20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.1047+3242G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206710 | |||||||
| chr2:162206833 | G | A | 1 | a0001c0002t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1047+3119C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206833 | |||||||
| chr2:162206869 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1047+3083G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206869 | |||||||
| chr2:162206886 | A | G | 1 | a0001c0002t0001g0049 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1047+3066T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162206886 | |||||||
| chr2:162207284 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047+2668A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207284 | |||||||
| chr2:162207403 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(16): Show |
24 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1047+2549G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207403 | |||||||
| chr2:162207714 | A | AT | 10 | a0001c0001t0001g0079 a0001c0001t0001g0147 a0001c0001t0001g0184 others(7): Show |
10 | HG00558.hp2 HG01891.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047+2237dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | |||||||
| chr2:162207714 | A | ATT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(8): Show |
16 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1047+2236_1047+223 others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | |||||||
| chr2:162207714 | A | ATTTT | 23 | a0001c0002t0001g0003 a0001c0002t0001g0005 a0001c0002t0001g0025 others(20): Show |
25 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1047+2234_1047+223 others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | |||||||
| chr2:162207714 | A | ATTTTT | 5 | a0001c0002t0001g0004 a0001c0002t0001g0044 a0001c0002t0001g0047 others(2): Show |
6 | NA18975.hp2 NA18989.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047+2233_1047+223 others(9): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207714 | |||||||
| chr2:162207753 | C | G | 1 | a0001c0002t0001g0044 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1047+2199G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207753 | |||||||
| chr2:162207811 | C | T | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0037 |
3 | HG00738.hp1 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1047+2141G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207811 | |||||||
| chr2:162207871 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1047+2081G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207871 | |||||||
| chr2:162207892 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1047+2060A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162207892 | |||||||
| chr2:162208122 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1047+1830C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208122 | |||||||
| chr2:162208129 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1047+1823C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208129 | |||||||
| chr2:162208254 | TA | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02074.hp1 NA18959.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047+1697delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208254 | |||||||
| chr2:162208278 | C | T | 3 | a0002c0005t0001g0065 a0002c0005t0002g0209 a0002c0005t0002g0210 |
3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1047+1674G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208278 | |||||||
| chr2:162208438 | T | C | 1 | a0001c0002t0001g0042 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1047+1514A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208438 | |||||||
| chr2:162208471 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1047+1481T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208471 | |||||||
| chr2:162208550 | T | C | 1 | a0001c0002t0001g0025 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1047+1402A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208550 | |||||||
| chr2:162208557 | A | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1047+1395T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208557 | |||||||
| chr2:162208815 | A | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1047+1137T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208815 | |||||||
| chr2:162208824 | GT | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(18): Show |
26 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1047+1127delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162208824 | |||||||
| chr2:162209004 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1047+948A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209004 | |||||||
| chr2:162209050 | A | G | 3 | a0001c0001t0001g0195 a0003c0006t0001g0085 a0003c0006t0001g0190 |
3 | HG02559.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1047+902T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209050 | |||||||
| chr2:162209099 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1047+853A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209099 | |||||||
| chr2:162209203 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1047+749C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209203 | |||||||
| chr2:162209363 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(49): Show |
60 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1047+589C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209363 | |||||||
| chr2:162209380 | A | G | 5 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0092 others(2): Show |
5 | HG02015.hp2 HG02074.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+572T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209380 | |||||||
| chr2:162209490 | A | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1047+462T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209490 | |||||||
| chr2:162209577 | A | AT | 5 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG02015.hp1 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047+374dupA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209577 | |||||||
| chr2:162209597 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1047+355C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209597 | |||||||
| chr2:162209809 | A | ATCAC | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047+139_1047+142d others(6): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209809 | |||||||
| chr2:162209898 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1047+54G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 12/25 | chr2 | 162209898 | |||||||
| chr2:162210015 | C | G | 9 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0199 others(6): Show |
9 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003-19G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210015 | |||||||
| chr2:162210171 | T | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0147 others(7): Show |
10 | HG00558.hp2 HG02155.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-175A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210171 | |||||||
| chr2:162210184 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1003-188C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210184 | |||||||
| chr2:162210281 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1003-285T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210281 | |||||||
| chr2:162210578 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1003-582C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210578 | |||||||
| chr2:162210808 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1003-812T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210808 | |||||||
| chr2:162210839 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1003-843C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210839 | |||||||
| chr2:162210931 | A | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1003-935T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210931 | |||||||
| chr2:162210947 | A | T | 15 | a0001c0002t0001g0003 a0001c0002t0001g0026 a0001c0002t0001g0027 others(12): Show |
16 | HG00738.hp1 HG01069.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1003-951T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162210947 | |||||||
| chr2:162211046 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1003-1050A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211046 | |||||||
| chr2:162211073 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0189 |
2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1003-1077C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211073 | |||||||
| chr2:162211641 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1003-1645T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211641 | |||||||
| chr2:162211832 | C | T | 2 | a0001c0001t0001g0103 a0001c0002t0001g0036 |
2 | HG01192.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1003-1836G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211832 | |||||||
| chr2:162211959 | C | T | 1 | a0001c0002t0001g0035 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1003-1963G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162211959 | |||||||
| chr2:162212404 | T | C | 6 | a0001c0001t0001g0195 a0002c0005t0001g0065 a0002c0005t0002g0209 others(3): Show |
6 | HG02280.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1002+1534A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212404 | |||||||
| chr2:162212493 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1002+1445A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212493 | |||||||
| chr2:162212538 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1002+1400C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212538 | |||||||
| chr2:162212548 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+1390C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212548 | |||||||
| chr2:162212642 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1002+1296A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212642 | |||||||
| chr2:162212771 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1002+1167T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212771 | |||||||
| chr2:162212799 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+1139A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212799 | |||||||
| chr2:162212993 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1002+945C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162212993 | |||||||
| chr2:162213054 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1002+884T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213054 | |||||||
| chr2:162213350 | T | C | 1 | a0001c0002t0001g0025 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1002+588A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213350 | |||||||
| chr2:162213362 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1002+576C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213362 | |||||||
| chr2:162213367 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1002+571C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213367 | |||||||
| chr2:162213374 | C | CA | 12 | a0001c0001t0001g0022 a0001c0001t0001g0070 a0001c0001t0001g0086 others(9): Show |
12 | HG01261.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002+563dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213374 | |||||||
| chr2:162213404 | C | CA | 7 | a0001c0001t0001g0017 a0001c0001t0001g0073 a0001c0001t0001g0191 others(4): Show |
8 | HG02145.hp1 HG02572.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1002+533dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213404 | |||||||
| chr2:162213424 | CA | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0084 others(14): Show |
18 | HG00609.hp2 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1002+513delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213424 | |||||||
| chr2:162213428 | A | C | 40 | a0001c0001t0001g0100 a0001c0001t0001g0195 a0001c0002t0001g0003 others(37): Show |
43 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1002+510T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213428 | |||||||
| chr2:162213518 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1002+420G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213518 | |||||||
| chr2:162213585 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1002+353G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213585 | |||||||
| chr2:162213601 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(66): Show |
79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.1002+337T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 11/25 | chr2 | 162213601 | |||||||
| chr2:162214086 | T | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-13A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214086 | |||||||
| chr2:162214197 | C | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-124G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214197 | |||||||
| chr2:162214527 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-454C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214527 | |||||||
| chr2:162214651 | C | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.867-578G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214651 | |||||||
| chr2:162214908 | G | C | 1 | a0001c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.867-835C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162214908 | |||||||
| chr2:162215032 | TA | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.866+865delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215032 | |||||||
| chr2:162215083 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.866+815C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215083 | |||||||
| chr2:162215185 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0092 others(2): Show |
5 | HG02015.hp2 HG02074.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.866+713C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215185 | |||||||
| chr2:162215216 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(66): Show |
79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.866+682C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215216 | |||||||
| chr2:162215553 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.866+345A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215553 | |||||||
| chr2:162215615 | T | G | 1 | a0001c0001t0001g0019 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.866+283A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215615 | |||||||
| chr2:162215706 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.866+192C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215706 | |||||||
| chr2:162215721 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0003g0211 |
3 | HG02970.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.866+177C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215721 | |||||||
| chr2:162215810 | C | T | 3 | a0002c0005t0001g0065 a0002c0005t0002g0209 a0002c0005t0002g0210 |
3 | HG02280.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.866+88G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 10/25 | chr2 | 162215810 | |||||||
| chr2:162216171 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.763-170C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216171 | |||||||
| chr2:162216318 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.763-317G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216318 | |||||||
| chr2:162216522 | G | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA19007.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.763-521C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216522 | |||||||
| chr2:162216550 | G | C | 12 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0184 others(9): Show |
12 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.763-549C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216550 | |||||||
| chr2:162216561 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.763-560T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216561 | |||||||
| chr2:162216572 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.763-571A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162216572 | |||||||
| chr2:162217212 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.762+774G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217212 | |||||||
| chr2:162217217 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.762+769T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217217 | |||||||
| chr2:162217530 | T | G | 1 | a0001c0003t0001g0081 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.762+456A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217530 | |||||||
| chr2:162217654 | G | A | 18 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(15): Show |
20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.762+332C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217654 | |||||||
| chr2:162217696 | A | G | 1 | a0002c0005t0001g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.762+290T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 9/25 | chr2 | 162217696 | |||||||
| chr2:162218378 | T | C | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.608-238A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218378 | |||||||
| chr2:162218450 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(20): Show |
28 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.608-310G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218450 | |||||||
| chr2:162218561 | T | TTAGA | 28 | a0001c0001t0001g0063 a0001c0001t0001g0071 a0001c0001t0001g0073 others(25): Show |
28 | HG00323.hp2 HG00609.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.608-425_608-422dup others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218561 | |||||||
| chr2:162218561 | TTAGA | T | 26 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(23): Show |
30 | HG00733.hp2 HG01175.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.608-425_608-422del others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218561 | |||||||
| chr2:162218561 | TTAGATAG others(1): Show |
T | 19 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(16): Show |
21 | HG00621.hp1 HG01257.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-429_608-422del others(8): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218561 | |||||||
| chr2:162218598 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.608-458A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218598 | |||||||
| chr2:162218754 | A | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.607+309T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218754 | |||||||
| chr2:162218755 | T | A | 1 | a0002c0005t0001g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.607+308A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162218755 | |||||||
| chr2:162219044 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.607+19C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 8/25 | chr2 | 162219044 | |||||||
| chr2:162219312 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-129G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 7/25 | chr2 | 162219312 | |||||||
| chr2:162219636 | T | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(44): Show |
54 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.486+217A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 7/25 | chr2 | 162219636 | |||||||
| chr2:162220181 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.414-256C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220181 | |||||||
| chr2:162220288 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.414-363G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220288 | |||||||
| chr2:162220373 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414-448G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220373 | |||||||
| chr2:162220830 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.414-905A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162220830 | |||||||
| chr2:162221032 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.414-1107T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221032 | |||||||
| chr2:162221323 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.414-1398T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221323 | |||||||
| chr2:162221330 | G | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.414-1405C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221330 | |||||||
| chr2:162221345 | T | A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG01168.hp1 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-1420A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221345 | |||||||
| chr2:162221524 | C | CA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(41): Show |
55 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.414-1600dupT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221524 | |||||||
| chr2:162221685 | T | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.414-1760A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221685 | |||||||
| chr2:162221691 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.414-1766T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221691 | |||||||
| chr2:162221793 | A | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | NA18941.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.413+1815T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162221793 | |||||||
| chr2:162222090 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(5): Show |
13 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+1518T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222090 | |||||||
| chr2:162222146 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0092 others(2): Show |
5 | HG02015.hp2 HG02074.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+1462G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222146 | |||||||
| chr2:162222396 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.413+1212A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222396 | |||||||
| chr2:162222501 | T | A | 1 | a0001c0001t0001g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.413+1107A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222501 | |||||||
| chr2:162222508 | T | A | 1 | a0001c0002t0001g0053 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.413+1100A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222508 | |||||||
| chr2:162222820 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.413+788G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162222820 | |||||||
| chr2:162223198 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.413+410G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162223198 | |||||||
| chr2:162223307 | C | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+301G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162223307 | |||||||
| chr2:162223582 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.413+26T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 6/25 | chr2 | 162223582 | |||||||
| chr2:162224122 | C | T | 1 | a0001c0002t0001g0025 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.360+344G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 5/25 | chr2 | 162224122 | |||||||
| chr2:162224283 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(67): Show |
80 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.360+183T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 5/25 | chr2 | 162224283 | |||||||
| chr2:162224578 | A | T | 1 | a0001c0001t0003g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286-38T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224578 | |||||||
| chr2:162224718 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.286-178T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224718 | |||||||
| chr2:162224766 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.286-226G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224766 | |||||||
| chr2:162224793 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0090 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.286-253T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224793 | |||||||
| chr2:162224922 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(66): Show |
79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.286-382G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162224922 | |||||||
| chr2:162225260 | G | A | 5 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0080 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+223C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162225260 | |||||||
| chr2:162225321 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.285+162T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162225321 | |||||||
| chr2:162225420 | G | A | 2 | a0002c0005t0001g0065 a0002c0005t0002g0209 |
2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.285+63C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 4/25 | chr2 | 162225420 | |||||||
| chr2:162225612 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.191-35G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225612 | |||||||
| chr2:162225776 | G | A | 1 | a0001c0002t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.191-199C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225776 | |||||||
| chr2:162225879 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.191-302T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225879 | |||||||
| chr2:162225885 | C | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(44): Show |
54 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.191-308G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162225885 | |||||||
| chr2:162226289 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.190+234A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226289 | |||||||
| chr2:162226370 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.190+153C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226370 | |||||||
| chr2:162226425 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.190+98G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226425 | |||||||
| chr2:162226432 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
9 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.190+91C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 3/25 | chr2 | 162226432 | |||||||
| chr2:162226627 | G | T | 1 | a0001c0001t0001g0006 | 2 | HG00735.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.92-6C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226627 | |||||||
| chr2:162226640 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-19A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226640 | |||||||
| chr2:162226791 | C | T | 15 | a0001c0002t0001g0003 a0001c0002t0001g0026 a0001c0002t0001g0027 others(12): Show |
16 | HG00738.hp1 HG01069.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-170G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226791 | |||||||
| chr2:162226796 | T | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.92-175A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162226796 | |||||||
| chr2:162227148 | C | A | 2 | a0002c0005t0001g0065 a0002c0005t0002g0209 |
2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.92-527G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227148 | |||||||
| chr2:162227204 | T | C | 2 | a0002c0005t0001g0065 a0002c0005t0002g0209 |
2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.92-583A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227204 | |||||||
| chr2:162227386 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.92-765T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227386 | |||||||
| chr2:162227970 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(66): Show |
79 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.92-1349G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162227970 | |||||||
| chr2:162228488 | T | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-1867A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228488 | |||||||
| chr2:162228595 | T | G | 1 | a0002c0005t0001g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-1974A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228595 | |||||||
| chr2:162228666 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.92-2045A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228666 | |||||||
| chr2:162228914 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.92-2293G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228914 | |||||||
| chr2:162228952 | G | A | 2 | a0002c0005t0001g0065 a0002c0005t0002g0209 |
2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.92-2331C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162228952 | |||||||
| chr2:162229381 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.92-2760C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229381 | |||||||
| chr2:162229470 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.92-2849T>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229470 | |||||||
| chr2:162229647 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.92-3026G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229647 | |||||||
| chr2:162229649 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.92-3028A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229649 | |||||||
| chr2:162229770 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.92-3149T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229770 | |||||||
| chr2:162229838 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.92-3217A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229838 | |||||||
| chr2:162229841 | A | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG02257.hp1 HG02970.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-3220T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229841 | |||||||
| chr2:162229850 | CAT | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(15): Show |
24 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.92-3231_92-3230del others(2): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229850 | |||||||
| chr2:162229919 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(67): Show |
80 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.92-3298T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162229919 | |||||||
| chr2:162230270 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.92-3649A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230270 | |||||||
| chr2:162230305 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.92-3684C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230305 | |||||||
| chr2:162230563 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.92-3942G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230563 | |||||||
| chr2:162230585 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.92-3964G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230585 | |||||||
| chr2:162230586 | G | A | 10 | a0001c0002t0001g0003 a0001c0002t0001g0035 a0001c0002t0001g0036 others(7): Show |
11 | HG01069.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-3965C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230586 | |||||||
| chr2:162230620 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-3999A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230620 | |||||||
| chr2:162230679 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.92-4058A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230679 | |||||||
| chr2:162230762 | TG | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-4142delC | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230762 | |||||||
| chr2:162230764 | G | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.92-4143C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230764 | |||||||
| chr2:162230915 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(65): Show |
78 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.92-4294G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162230915 | |||||||
| chr2:162231260 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-4639A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231260 | |||||||
| chr2:162231470 | C | T | 18 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(15): Show |
20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-4849G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231470 | |||||||
| chr2:162231644 | T | C | 1 | a0002c0005t0001g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-5023A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231644 | |||||||
| chr2:162231769 | G | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0204 |
3 | HG02647.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.92-5148C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162231769 | |||||||
| chr2:162232297 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.92-5676G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232297 | |||||||
| chr2:162232433 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-5812G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232433 | |||||||
| chr2:162232496 | G | T | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-5875C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232496 | |||||||
| chr2:162232704 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-6083G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232704 | |||||||
| chr2:162232705 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.92-6084C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162232705 | |||||||
| chr2:162233152 | A | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0191 others(7): Show |
11 | HG02145.hp1 HG02630.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-6531T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233152 | |||||||
| chr2:162233316 | C | T | 2 | a0001c0001t0001g0020 a0004c0008t0001g0021 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.92-6695G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233316 | |||||||
| chr2:162233356 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-6735G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233356 | |||||||
| chr2:162233401 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.92-6780C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233401 | |||||||
| chr2:162233756 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.92-7135G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233756 | |||||||
| chr2:162233916 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.92-7295G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162233916 | |||||||
| chr2:162234099 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-7478G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234099 | |||||||
| chr2:162234102 | C | T | 2 | a0001c0002t0001g0004 a0001c0002t0001g0044 |
3 | NA19004.hp1 NA19058.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.92-7481G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234102 | |||||||
| chr2:162234328 | A | C | 1 | a0001c0001t0003g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.92-7707T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234328 | |||||||
| chr2:162234345 | G | A | 18 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0025 others(15): Show |
20 | HG00621.hp1 HG02015.hp1 HG03654.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-7724C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234345 | |||||||
| chr2:162234350 | C | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18992.hp2 NA18994.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.92-7729G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234350 | |||||||
| chr2:162234406 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.92-7785A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234406 | |||||||
| chr2:162234460 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-7839C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234460 | |||||||
| chr2:162234467 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG02257.hp2 HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.92-7846A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234467 | |||||||
| chr2:162234633 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.92-8012C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234633 | |||||||
| chr2:162234674 | T | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.92-8053A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234674 | |||||||
| chr2:162234787 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+8121C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234787 | |||||||
| chr2:162234791 | C | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+8117G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234791 | |||||||
| chr2:162234816 | C | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+8092G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234816 | |||||||
| chr2:162234881 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.91+8027C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234881 | |||||||
| chr2:162234917 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+7991A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234917 | |||||||
| chr2:162234938 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.91+7970C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162234938 | |||||||
| chr2:162235034 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+7874G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235034 | |||||||
| chr2:162235055 | G | T | 5 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0080 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+7853C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235055 | |||||||
| chr2:162235157 | C | G | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+7751G>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235157 | |||||||
| chr2:162235166 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.91+7742G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235166 | |||||||
| chr2:162235177 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+7731A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235177 | |||||||
| chr2:162235243 | T | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(58): Show |
66 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.91+7665A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235243 | |||||||
| chr2:162235244 | T | G | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(58): Show |
66 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.91+7664A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235244 | |||||||
| chr2:162235342 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0003g0211 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.91+7566C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235342 | |||||||
| chr2:162235457 | T | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
10 | HG02145.hp1 HG02630.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+7451A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235457 | |||||||
| chr2:162235848 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.91+7060A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235848 | |||||||
| chr2:162235974 | G | A | 2 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.91+6934C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162235974 | |||||||
| chr2:162236036 | T | C | 4 | a0001c0001t0002g0208 a0002c0005t0001g0065 a0002c0005t0002g0209 others(1): Show |
4 | HG02280.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+6872A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236036 | |||||||
| chr2:162236054 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+6854A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236054 | |||||||
| chr2:162236108 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.91+6800A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236108 | |||||||
| chr2:162236188 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+6720C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236188 | |||||||
| chr2:162236303 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+6605G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236303 | |||||||
| chr2:162236324 | A | C | 1 | a0001c0002t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.91+6584T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236324 | |||||||
| chr2:162236448 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.91+6460C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236448 | |||||||
| chr2:162236448 | GT | G | 32 | a0001c0001t0001g0020 a0001c0002t0001g0003 a0001c0002t0001g0004 others(29): Show |
35 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.91+6459delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236448 | |||||||
| chr2:162236496 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+6412A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236496 | |||||||
| chr2:162236594 | A | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+6314T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236594 | |||||||
| chr2:162236617 | T | TG | 67 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(64): Show |
77 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.91+6290dupC | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236617 | |||||||
| chr2:162236620 | G | T | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.91+6288C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236620 | |||||||
| chr2:162236676 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.91+6232A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236676 | |||||||
| chr2:162236819 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG00609.hp1 NA18946.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.91+6089A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236819 | |||||||
| chr2:162236838 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG00609.hp1 NA18946.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.91+6070T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236838 | |||||||
| chr2:162236862 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0066 others(7): Show |
15 | HG00639.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.91+6046T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162236862 | |||||||
| chr2:162237003 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.91+5905A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237003 | |||||||
| chr2:162237171 | TTGAC | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG02257.hp2 HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.91+5733_91+5736del others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237171 | |||||||
| chr2:162237377 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.91+5531C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237377 | |||||||
| chr2:162237663 | C | A | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG01168.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+5245G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237663 | |||||||
| chr2:162237667 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.91+5241A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237667 | |||||||
| chr2:162237883 | C | T | 4 | a0001c0001t0002g0208 a0002c0005t0001g0065 a0002c0005t0002g0209 others(1): Show |
4 | HG02280.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5025G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162237883 | |||||||
| chr2:162238045 | GT | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+4862delA | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238045 | |||||||
| chr2:162238047 | T | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+4861A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238047 | |||||||
| chr2:162238131 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91+4777G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238131 | |||||||
| chr2:162238136 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.91+4772T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238136 | |||||||
| chr2:162238171 | TC | T | 6 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(3): Show |
6 | HG02258.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+4736delG | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238171 | |||||||
| chr2:162238398 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.91+4510G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238398 | |||||||
| chr2:162238539 | ATTTC | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+4365_91+4368del others(4): Show |
FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238539 | |||||||
| chr2:162238555 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.91+4353A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238555 | |||||||
| chr2:162238769 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18992.hp2 NA18994.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.91+4139G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238769 | |||||||
| chr2:162238847 | A | G | 2 | a0001c0007t0001g0056 a0001c0007t0001g0057 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.91+4061T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238847 | |||||||
| chr2:162238855 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+4053G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238855 | |||||||
| chr2:162238992 | T | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0198 a0001c0001t0001g0199 others(7): Show |
11 | HG02258.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+3916A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162238992 | |||||||
| chr2:162239040 | A | G | 2 | a0001c0001t0001g0020 a0004c0008t0001g0021 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.91+3868T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239040 | |||||||
| chr2:162239056 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.91+3852A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239056 | |||||||
| chr2:162239133 | C | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG01891.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.91+3775G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239133 | |||||||
| chr2:162239409 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.91+3499G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239409 | |||||||
| chr2:162239502 | TA | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+3405delT | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162239502 | |||||||
| chr2:162240049 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+2859A>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240049 | |||||||
| chr2:162240115 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91+2793C>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240115 | |||||||
| chr2:162240269 | A | C | 2 | a0001c0002t0001g0029 a0001c0002t0001g0030 |
2 | HG00621.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.91+2639T>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240269 | |||||||
| chr2:162240377 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+2531C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240377 | |||||||
| chr2:162240407 | T | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
10 | HG02145.hp1 HG02630.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+2501A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240407 | |||||||
| chr2:162240423 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91+2485G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240423 | |||||||
| chr2:162240424 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.91+2484C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240424 | |||||||
| chr2:162240641 | C | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0198 a0001c0001t0001g0199 others(7): Show |
11 | HG02258.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+2267G>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240641 | |||||||
| chr2:162240961 | C | T | 3 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 |
3 | HG00738.hp1 HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.91+1947G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162240961 | |||||||
| chr2:162241090 | G | C | 38 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(35): Show |
41 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.91+1818C>G | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241090 | |||||||
| chr2:162241460 | G | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(35): Show |
41 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.91+1448C>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241460 | |||||||
| chr2:162241469 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(30): Show |
36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.91+1439G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241469 | |||||||
| chr2:162241526 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.91+1382G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241526 | |||||||
| chr2:162241635 | A | G | 38 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(35): Show |
41 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.91+1273T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162241635 | |||||||
| chr2:162242045 | C | T | 1 | a0001c0002t0001g0025 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.91+863G>A | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242045 | |||||||
| chr2:162242185 | A | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+723T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242185 | |||||||
| chr2:162242334 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.91+574T>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242334 | |||||||
| chr2:162242403 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.91+505A>T | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 2/25 | chr2 | 162242403 | |||||||
| chr2:162243079 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7-87A>C | FAP | ENSG00000078098.15 | transcript | ENST00000188790.9 | protein_coding | 1/25 | chr2 | 162243079 |