Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 92 |
| ensemblid | ENSG00000121989.15 |
| hgncid | 173 |
| symbol | ACVR2A |
| name | activin A receptor type 2A |
| refseq_nuc | NM_001616.5 |
| refseq_prot | NP_001607.1 |
| ensembl_nuc | ENST00000241416.12 |
| ensembl_prot | ENSP00000241416.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 147845029 |
| end | 147930822 |
| strand | + |
| ver | v1.2 |
| region | chr2:147845029-147930822 |
| region5000 | chr2:147840029-147935822 |
| regionname0 | ACVR2A_chr2_147845029_147930822 |
| regionname5000 | ACVR2A_chr2_147840029_147935822 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 513 | 336 | 72 | 64 | 144 | 14 | 40 | 113 | ACVR2A_chr2_147840029_147935822 | ACVR2A | MGAAA others(508): Show |
chr2 | 147840029 | 147935822 |
| a0002 | 0/0 | 513 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | MGAAA others(508): Show |
chr2 | 147840029 | 147935822 |
| a0003 | 0/0 | 513 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | MGAAA others(508): Show |
chr2 | 147840029 | 147935822 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1539 | 195 | 48 | 30 | 83 | 8 | 24 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 | ||
| a0001c0002 | 0/0 | 1539 | 135 | 21 | 32 | 60 | 6 | 16 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 | ||
| a0001c0003 | 0/0 | 1539 | 2 | 0 | 2 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 | ||
| a0001c0004 | 0/0 | 1539 | 2 | 2 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 | ||
| a0001c0005 | 0/0 | 1539 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 | ||
| a0001c0008 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 | ||
| a0002c0007 | 0/0 | 1539 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 | ||
| a0003c0006 | 0/0 | 1539 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | ATGGG others(1534): Show |
chr2 | 147840029 | 147935822 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5214 | 54 | 38 | 10 | 0 | 4 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0002 | 0/0 | 5214 | 87 | 2 | 12 | 54 | 4 | 15 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0003 | 0/0 | 5214 | 41 | 3 | 8 | 22 | 0 | 8 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0004 | 0/0 | 5204 | 4 | 0 | 0 | 4 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5199): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0006 | 0/0 | 5214 | 2 | 0 | 0 | 2 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0010 | 0/0 | 5187 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5182): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0014 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0016 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0017 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0018 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0019 | 0/1 | 5213 | 1 | 0 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5208): Show |
chr2 | 147840029 | 147935822 |
| a0001c0001t0021 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0001 | 0/0 | 5214 | 125 | 18 | 29 | 58 | 6 | 14 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0005 | 0/0 | 5214 | 2 | 0 | 0 | 0 | 0 | 2 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0007 | 0/0 | 5214 | 2 | 0 | 2 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0009 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0011 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0012 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0013 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0015 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0002t0020 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0003t0002 | 0/0 | 5214 | 2 | 0 | 2 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0004t0001 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0005t0001 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0001c0008t0004 | 0/0 | 5204 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5199): Show |
chr2 | 147840029 | 147935822 |
| a0002c0007t0001 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| a0003c0006t0008 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | GTCTG others(5209): Show |
chr2 | 147840029 | 147935822 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0018g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0019g0284 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0001t0021g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0005g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0013g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0015g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0002t0020g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0005t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0001c0008t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0002c0007t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| a0003c0006t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0139 | EUR | GBR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0041 | EUR | GBR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | GBR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | FIN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0243 | EUR | FIN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0126 | EUR | FIN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | FIN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00738 | hp1 | a0001 | c0002 | t0007 | g0100 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0210 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0211 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01175 | hp1 | a0001 | c0002 | t0007 | g0050 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0069 | EUR | IBS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01943 | hp2 | a0001 | c0002 | t0015 | g0107 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02129 | hp2 | a0002 | c0007 | t0001 | g0089 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | CDX | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | CDX | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | CDX | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | CDX | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02258 | hp1 | a0001 | c0002 | t0012 | g0144 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02523 | hp2 | a0001 | c0002 | t0013 | g0046 | EAS | KHV | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02615 | hp1 | a0001 | c0002 | t0011 | g0112 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0262 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0162 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0014 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0280 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0167 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03491 | hp2 | a0001 | c0002 | t0005 | g0010 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03492 | hp1 | a0001 | c0002 | t0005 | g0010 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0276 | AFR | ESN | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0296 | SAS | PJL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0273 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0129 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | STU | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | CHB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18951 | hp2 | a0001 | c0002 | t0020 | g0040 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18974 | hp2 | a0003 | c0006 | t0008 | g0086 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19003 | hp2 | a0001 | c0005 | t0001 | g0007 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | LWK | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | LWK | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19081 | hp1 | a0001 | c0001 | t0010 | g0203 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | YRI | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | YRI | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ASW | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0058 | EUR | TSI | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0227 | EUR | TSI | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02109 | hp1 | a0001 | c0002 | t0009 | g0172 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | USA | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0261 | AFR | USA | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | USA | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| NA21309 | hp2 | a0001 | c0008 | t0004 | g0125 | AFR | LWK | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0019 | g0284 | REF | REF | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0180 | REF | REF | ACVR2A_chr2_147840029_147935822 | ACVR2A | chr2 | 147840029 | 147935822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147899822 | C | T | 1 | a0002 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.452C>T | p.Ala151Val | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/11 | 576/5214 | 452/1542 | 151/513 | chr2 | 147899822 | |||
| chr2:147927251 | C | T | 1 | a0003 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.1519C>T | p.Pro507Ser | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 1643/5214 | 1519/1542 | 507/513 | chr2 | 147927251 | |||
| chr2:147927254 | C | T | 1 | a0003 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.1522C>T | p.Pro508Ser | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 1646/5214 | 1522/1542 | 508/513 | chr2 | 147927254 | |||
| chr2:147930821 | G | A | 1 | a0001 | 2 | HG02258.hp1 HG02630.hp1 |
splice_region_variant | LOW | c.*3547G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | chr2 | 147930821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147896485 | G | A | 1 | a0001c0003 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.240G>A | p.Leu80Leu | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/11 | 364/5214 | 240/1542 | 80/513 | chr2 | 147896485 | |||
| chr2:147899548 | G | A | 4 | a0001c0002 a0001c0005 a0002c0007 others(1): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
synonymous_variant | LOW | c.354G>A | p.Pro118Pro | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 3/11 | 478/5214 | 354/1542 | 118/513 | chr2 | 147899548 | |||
| chr2:147917349 | T | C | 1 | a0001c0005 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.739T>C | p.Leu247Leu | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/11 | 863/5214 | 739/1542 | 247/513 | chr2 | 147917349 | |||
| chr2:147917393 | G | C | 1 | a0001c0004 | 2 | HG02615.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.783G>C | p.Val261Val | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/11 | 907/5214 | 783/1542 | 261/513 | chr2 | 147917393 | |||
| chr2:147926126 | A | C | 1 | a0001c0008 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1312A>C | p.Arg438Arg | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 10/11 | 1436/5214 | 1312/1542 | 438/513 | chr2 | 147926126 | |||
| chr2:147927253 | T | C | 1 | a0003c0006 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.1521T>C | p.Pro507Pro | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 1645/5214 | 1521/1542 | 507/513 | chr2 | 147927253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147927336 | A | G | 1 | a0001c0001t0021 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 62 | chr2 | 147927336 | ||||||
| chr2:147927998 | A | G | 1 | a0001c0002t0020 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*724A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 724 | chr2 | 147927998 | ||||||
| chr2:147928107 | C | A | 1 | a0003c0006t0008 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 833 | chr2 | 147928107 | ||||||
| chr2:147928108 | A | T | 1 | a0003c0006t0008 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*834A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 834 | chr2 | 147928108 | ||||||
| chr2:147928858 | A | C | 1 | a0003c0006t0008 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1584A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 1584 | chr2 | 147928858 | ||||||
| chr2:147928859 | C | A | 1 | a0003c0006t0008 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1585C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 1585 | chr2 | 147928859 | ||||||
| chr2:147928913 | T | C | 1 | a0001c0002t0005 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1639T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 1639 | chr2 | 147928913 | ||||||
| chr2:147929320 | T | C | 1 | a0001c0002t0009 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2046T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2046 | chr2 | 147929320 | ||||||
| chr2:147929364 | TTTCTTTT others(20): Show |
T | 1 | a0001c0001t0010 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2091_*2117delTTCT others(23): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2091 | chr2 | 147929364 | ||||||
| chr2:147929377 | G | GTT | 13 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0005 others(10): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*2104_*2105dupTT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2106 | INFO_REALIGN_3_PRIME | chr2 | 147929377 | |||||
| chr2:147929492 | A | T | 3 | a0001c0001t0002 a0001c0001t0010 a0001c0003t0002 |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2218A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2218 | chr2 | 147929492 | ||||||
| chr2:147929650 | T | C | 1 | a0001c0001t0021 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2376T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2376 | chr2 | 147929650 | ||||||
| chr2:147929672 | T | C | 1 | a0001c0001t0006 | 2 | HG02071.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2398T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2398 | chr2 | 147929672 | ||||||
| chr2:147929762 | G | C | 1 | a0001c0001t0006 | 2 | HG02071.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2488G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2488 | chr2 | 147929762 | ||||||
| chr2:147929773 | T | C | 2 | a0001c0002t0011 a0001c0002t0012 |
2 | HG02258.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2499T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2499 | chr2 | 147929773 | ||||||
| chr2:147929776 | G | C | 1 | a0001c0002t0013 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2502G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2502 | chr2 | 147929776 | ||||||
| chr2:147929796 | A | G | 1 | a0001c0001t0021 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2522 | chr2 | 147929796 | ||||||
| chr2:147929994 | T | C | 1 | a0001c0001t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2720T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2720 | chr2 | 147929994 | ||||||
| chr2:147930162 | A | C | 2 | a0001c0001t0003 a0001c0001t0006 |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2888A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 2888 | chr2 | 147930162 | ||||||
| chr2:147930306 | C | A | 1 | a0001c0002t0007 | 2 | HG00738.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3032C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3032 | chr2 | 147930306 | ||||||
| chr2:147930347 | G | T | 1 | a0001c0002t0009 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3073G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3073 | chr2 | 147930347 | ||||||
| chr2:147930347 | GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0004 a0001c0008t0004 |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3081_*3090delGTTT others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3081 | INFO_REALIGN_3_PRIME | chr2 | 147930347 | |||||
| chr2:147930355 | G | T | 1 | a0001c0001t0002 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3081G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3081 | chr2 | 147930355 | ||||||
| chr2:147930355 | GT | G | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(13): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*3098delT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3098 | INFO_REALIGN_3_PRIME | chr2 | 147930355 | |||||
| chr2:147930361 | T | G | 1 | a0001c0002t0015 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3087T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3087 | chr2 | 147930361 | ||||||
| chr2:147930362 | T | G | 2 | a0001c0001t0016 a0001c0001t0017 |
2 | HG02622.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3088T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3088 | chr2 | 147930362 | ||||||
| chr2:147930513 | T | C | 1 | a0001c0001t0016 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3239T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3239 | chr2 | 147930513 | ||||||
| chr2:147930605 | A | G | 1 | a0001c0002t0012 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3331A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | 3331 | chr2 | 147930605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:147845307 | C | A | 2 | a0001c0001t0004g0021 a0001c0001t0004g0022 |
2 | NA18974.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.55+100C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845307 | |||||||
| chr2:147845348 | G | GCCCC | 23 | a0001c0001t0001g0094 a0001c0002t0001g0007 a0001c0002t0001g0095 others(20): Show |
25 | HG00544.hp2 HG00738.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.55+150_55+153dupCC others(2): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147845348 | ||||||
| chr2:147845348 | G | GCCCCC | 48 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0048 others(45): Show |
52 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.55+149_55+153dupCC others(3): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147845348 | ||||||
| chr2:147845348 | G | GCCCCCC | 24 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
26 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.55+148_55+153dupCC others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147845348 | ||||||
| chr2:147845348 | G | GCCCCCCC others(5): Show |
1 | a0001c0002t0001g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.55+142_55+153dupCC others(10): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147845348 | ||||||
| chr2:147845348 | GC | G | 98 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(95): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.55+153delC | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147845348 | ||||||
| chr2:147845348 | GCC | G | 29 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0003g0002 others(26): Show |
38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.55+152_55+153delCC | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147845348 | ||||||
| chr2:147845359 | C | G | 1 | a0001c0001t0002g0306 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.55+152C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845359 | |||||||
| chr2:147845361 | G | C | 1 | a0001c0002t0001g0023 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.55+154G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845361 | |||||||
| chr2:147845431 | A | T | 1 | a0001c0001t0002g0019 | 2 | NA18941.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.55+224A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845431 | |||||||
| chr2:147845517 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0192 others(3): Show |
8 | HG00735.hp2 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+310A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845517 | |||||||
| chr2:147845556 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.55+349G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845556 | |||||||
| chr2:147845755 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.55+548C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845755 | |||||||
| chr2:147845934 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0277 |
2 | HG01167.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.55+727A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845934 | |||||||
| chr2:147845985 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.55+778T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147845985 | |||||||
| chr2:147846053 | G | C | 6 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+846G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147846053 | |||||||
| chr2:147846171 | A | G | 1 | a0001c0002t0001g0047 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.55+964A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147846171 | |||||||
| chr2:147846246 | C | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+1039C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147846246 | |||||||
| chr2:147846569 | G | C | 1 | a0001c0001t0002g0194 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.55+1362G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147846569 | |||||||
| chr2:147847050 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55+1843A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147847050 | |||||||
| chr2:147847124 | T | G | 24 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.55+1917T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147847124 | |||||||
| chr2:147847461 | T | G | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55+2254T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147847461 | |||||||
| chr2:147847494 | A | G | 6 | a0001c0001t0003g0020 a0001c0001t0003g0275 a0001c0001t0003g0302 others(3): Show |
7 | HG00609.hp1 HG00673.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+2287A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147847494 | |||||||
| chr2:147847511 | T | A | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG00609.hp2 NA18986.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.55+2304T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147847511 | |||||||
| chr2:147847791 | C | G | 1 | a0001c0001t0003g0275 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.55+2584C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147847791 | |||||||
| chr2:147848037 | T | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG00642.hp2 HG00741.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.55+2830T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147848037 | |||||||
| chr2:147848423 | C | G | 1 | a0001c0002t0001g0030 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.55+3216C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147848423 | |||||||
| chr2:147848662 | T | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+3455T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147848662 | |||||||
| chr2:147848674 | G | C | 4 | a0001c0002t0001g0031 a0001c0002t0001g0058 a0001c0002t0001g0126 others(1): Show |
5 | HG00323.hp1 HG02698.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+3467G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147848674 | |||||||
| chr2:147849062 | C | G | 1 | a0001c0001t0002g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+3855C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849062 | |||||||
| chr2:147849084 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.55+3877A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849084 | |||||||
| chr2:147849105 | A | C | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.55+3898A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849105 | |||||||
| chr2:147849565 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.55+4358G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849565 | |||||||
| chr2:147849641 | G | T | 33 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(30): Show |
42 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.55+4434G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849641 | |||||||
| chr2:147849738 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.55+4531A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849738 | |||||||
| chr2:147849785 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55+4578A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849785 | |||||||
| chr2:147849813 | C | T | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.55+4606C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849813 | |||||||
| chr2:147849824 | T | A | 1 | a0001c0002t0001g0059 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.55+4617T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849824 | |||||||
| chr2:147849844 | T | TAAG | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(3): Show |
6 | HG00408.hp1 HG03516.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+4639_55+4641dup others(3): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147849844 | ||||||
| chr2:147849869 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.55+4662G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147849869 | |||||||
| chr2:147850078 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.55+4871C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147850078 | |||||||
| chr2:147850239 | G | C | 91 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.55+5032G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147850239 | |||||||
| chr2:147850279 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.55+5072C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147850279 | |||||||
| chr2:147850499 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.55+5292C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147850499 | |||||||
| chr2:147850542 | T | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0127 |
2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.55+5335T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147850542 | |||||||
| chr2:147850670 | AT | A | 95 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(92): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.55+5465delT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147850670 | ||||||
| chr2:147850987 | G | C | 283 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(280): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.55+5780G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147850987 | |||||||
| chr2:147851268 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.55+6061C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147851268 | |||||||
| chr2:147851292 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.55+6085A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147851292 | |||||||
| chr2:147851508 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
7 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.55+6301T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147851508 | |||||||
| chr2:147851566 | A | G | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.55+6359A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147851566 | |||||||
| chr2:147851771 | C | G | 1 | a0001c0001t0002g0169 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.55+6564C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147851771 | |||||||
| chr2:147852063 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55+6856T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852063 | |||||||
| chr2:147852090 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.55+6883T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852090 | |||||||
| chr2:147852140 | G | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+6933G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852140 | |||||||
| chr2:147852256 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.55+7049G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852256 | |||||||
| chr2:147852429 | C | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+7222C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852429 | |||||||
| chr2:147852645 | T | A | 1 | a0001c0001t0002g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.55+7438T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852645 | |||||||
| chr2:147852648 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.55+7441G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852648 | |||||||
| chr2:147852661 | C | T | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+7454C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852661 | |||||||
| chr2:147852755 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.55+7548C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852755 | |||||||
| chr2:147852875 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+7668C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147852875 | |||||||
| chr2:147853034 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.55+7827C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853034 | |||||||
| chr2:147853176 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(1): Show |
4 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+7969G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853176 | |||||||
| chr2:147853277 | A | G | 1 | a0001c0002t0001g0057 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.55+8070A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853277 | |||||||
| chr2:147853279 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+8072T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853279 | |||||||
| chr2:147853451 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.55+8244C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853451 | |||||||
| chr2:147853501 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.55+8294G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853501 | |||||||
| chr2:147853760 | C | T | 2 | a0001c0004t0001g0261 a0001c0004t0001g0262 |
2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.55+8553C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853760 | |||||||
| chr2:147853781 | T | C | 2 | a0001c0002t0011g0112 a0001c0002t0012g0144 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.55+8574T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853781 | |||||||
| chr2:147853892 | G | A | 2 | a0001c0002t0001g0033 a0001c0002t0001g0034 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.55+8685G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853892 | |||||||
| chr2:147853959 | T | G | 33 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(30): Show |
42 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.55+8752T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853959 | |||||||
| chr2:147853974 | A | C | 2 | a0001c0001t0003g0299 a0001c0001t0003g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.55+8767A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147853974 | |||||||
| chr2:147854112 | G | A | 1 | a0001c0001t0006g0283 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.55+8905G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854112 | |||||||
| chr2:147854154 | C | G | 1 | a0001c0001t0003g0298 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.55+8947C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854154 | |||||||
| chr2:147854206 | A | G | 1 | a0001c0001t0003g0298 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.55+8999A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854206 | |||||||
| chr2:147854220 | T | C | 1 | a0001c0001t0004g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.55+9013T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854220 | |||||||
| chr2:147854481 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.55+9274C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854481 | |||||||
| chr2:147854528 | T | G | 2 | a0001c0002t0011g0112 a0001c0002t0012g0144 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.55+9321T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854528 | |||||||
| chr2:147854585 | A | G | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.55+9378A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854585 | |||||||
| chr2:147854660 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0200 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.55+9453A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854660 | |||||||
| chr2:147854798 | C | T | 1 | a0001c0001t0017g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.55+9591C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854798 | |||||||
| chr2:147854955 | T | C | 2 | a0001c0002t0001g0060 a0001c0002t0001g0101 |
2 | HG02083.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.55+9748T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854955 | |||||||
| chr2:147854959 | A | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+9752A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147854959 | |||||||
| chr2:147855119 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.55+9912A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855119 | |||||||
| chr2:147855144 | T | A | 1 | a0001c0002t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.55+9937T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855144 | |||||||
| chr2:147855224 | G | A | 24 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.55+10017G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855224 | |||||||
| chr2:147855238 | T | C | 24 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.55+10031T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855238 | |||||||
| chr2:147855266 | A | G | 1 | a0001c0002t0013g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.55+10059A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855266 | |||||||
| chr2:147855362 | G | A | 2 | a0001c0001t0003g0188 a0001c0001t0003g0280 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.55+10155G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855362 | |||||||
| chr2:147855425 | A | T | 1 | a0001c0001t0002g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.55+10218A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855425 | |||||||
| chr2:147855505 | G | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
7 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+10298G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855505 | |||||||
| chr2:147855557 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55+10350G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855557 | |||||||
| chr2:147855794 | T | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+10587T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147855794 | |||||||
| chr2:147856080 | C | G | 1 | a0001c0002t0001g0056 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.55+10873C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856080 | |||||||
| chr2:147856090 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+10883T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856090 | |||||||
| chr2:147856169 | A | G | 2 | a0001c0001t0021g0276 a0001c0002t0001g0025 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.55+10962A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856169 | |||||||
| chr2:147856337 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55+11130G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856337 | |||||||
| chr2:147856531 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
7 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+11324A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856531 | |||||||
| chr2:147856560 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+11353A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856560 | |||||||
| chr2:147856586 | A | C | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(1): Show |
4 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+11379A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856586 | |||||||
| chr2:147856605 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0277 |
2 | HG01167.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.55+11398A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856605 | |||||||
| chr2:147856831 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.55+11624C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856831 | |||||||
| chr2:147856969 | T | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+11762T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147856969 | |||||||
| chr2:147857090 | G | T | 12 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(9): Show |
12 | HG00738.hp1 HG01175.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.55+11883G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857090 | |||||||
| chr2:147857117 | T | G | 1 | a0001c0001t0002g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.55+11910T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857117 | |||||||
| chr2:147857204 | G | C | 1 | a0001c0001t0003g0002 | 4 | NA18951.hp1 NA18957.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+11997G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857204 | |||||||
| chr2:147857254 | A | C | 2 | a0001c0002t0011g0112 a0001c0002t0012g0144 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.55+12047A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857254 | |||||||
| chr2:147857412 | A | C | 3 | a0001c0001t0002g0165 a0001c0001t0002g0254 a0001c0001t0002g0255 |
3 | HG01175.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.55+12205A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857412 | |||||||
| chr2:147857525 | T | C | 1 | a0001c0002t0001g0061 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.55+12318T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857525 | |||||||
| chr2:147857532 | T | TA | 16 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0001t0001g0148 others(13): Show |
17 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.55+12344dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147857532 | ||||||
| chr2:147857532 | TA | T | 15 | a0001c0001t0001g0200 a0001c0001t0001g0260 a0001c0001t0001g0266 others(12): Show |
15 | HG01069.hp2 HG01168.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.55+12344delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147857532 | ||||||
| chr2:147857544 | A | C | 2 | a0001c0001t0003g0297 a0001c0001t0021g0276 |
2 | HG03516.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.55+12337A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857544 | |||||||
| chr2:147857547 | A | C | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.55+12340A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857547 | |||||||
| chr2:147857548 | A | C | 2 | a0001c0001t0001g0267 a0001c0002t0001g0091 |
2 | HG02486.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.55+12341A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857548 | |||||||
| chr2:147857552 | C | A | 15 | a0001c0001t0001g0173 a0001c0001t0002g0147 a0001c0002t0001g0026 others(12): Show |
15 | HG00738.hp1 HG01175.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.55+12345C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857552 | |||||||
| chr2:147857782 | A | G | 3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0168 |
3 | HG02071.hp1 NA19085.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.55+12575A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857782 | |||||||
| chr2:147857828 | TA | T | 29 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(26): Show |
38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.55+12631delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147857828 | ||||||
| chr2:147857877 | A | G | 1 | a0001c0001t0006g0283 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.55+12670A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857877 | |||||||
| chr2:147857918 | T | C | 3 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0111 |
3 | HG01069.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.55+12711T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857918 | |||||||
| chr2:147857918 | T | G | 1 | a0001c0002t0001g0128 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.55+12711T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857918 | |||||||
| chr2:147857937 | G | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+12730G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857937 | |||||||
| chr2:147857961 | C | T | 95 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(92): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.55+12754C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147857961 | |||||||
| chr2:147858262 | T | G | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.55+13055T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147858262 | |||||||
| chr2:147858314 | A | G | 2 | a0001c0002t0001g0088 a0002c0007t0001g0089 |
2 | HG02129.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.55+13107A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147858314 | |||||||
| chr2:147858695 | C | T | 1 | a0001c0001t0016g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.55+13488C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147858695 | |||||||
| chr2:147858883 | T | G | 2 | a0001c0001t0002g0204 a0001c0001t0010g0203 |
2 | NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.55+13676T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147858883 | |||||||
| chr2:147858934 | A | T | 1 | a0001c0001t0002g0253 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.55+13727A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147858934 | |||||||
| chr2:147858993 | A | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+13786A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147858993 | |||||||
| chr2:147859120 | T | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+13913T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859120 | |||||||
| chr2:147859143 | A | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+13936A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859143 | |||||||
| chr2:147859317 | G | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+14110G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859317 | |||||||
| chr2:147859419 | A | T | 4 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0002g0251 others(1): Show |
4 | HG00558.hp1 NA18981.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+14212A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859419 | |||||||
| chr2:147859489 | C | CA | 18 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0148 others(15): Show |
20 | HG00099.hp1 HG00408.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.55+14296dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147859489 | ||||||
| chr2:147859641 | C | G | 2 | a0001c0001t0016g0162 a0001c0001t0017g0167 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.55+14434C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859641 | |||||||
| chr2:147859723 | G | A | 95 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(92): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.55+14516G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859723 | |||||||
| chr2:147859751 | A | G | 1 | a0001c0002t0001g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55+14544A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859751 | |||||||
| chr2:147859763 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.55+14556A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859763 | |||||||
| chr2:147859795 | G | A | 1 | a0001c0002t0001g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.55+14588G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859795 | |||||||
| chr2:147859811 | C | G | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.55+14604C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859811 | |||||||
| chr2:147859828 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.55+14621T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859828 | |||||||
| chr2:147859829 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.55+14622C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859829 | |||||||
| chr2:147859847 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+14640C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859847 | |||||||
| chr2:147859863 | ACAGAAGC others(4): Show |
A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+14669_55+14679d others(13): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147859863 | ||||||
| chr2:147859956 | A | T | 1 | a0001c0001t0002g0197 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.55+14749A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859956 | |||||||
| chr2:147859992 | G | T | 3 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0306 |
3 | NA18962.hp1 NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.55+14785G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147859992 | |||||||
| chr2:147860047 | A | G | 1 | a0001c0002t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.55+14840A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147860047 | |||||||
| chr2:147860216 | G | C | 1 | a0001c0002t0013g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.55+15009G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147860216 | |||||||
| chr2:147860316 | G | A | 11 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(8): Show |
11 | HG00738.hp1 HG01175.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.55+15109G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147860316 | |||||||
| chr2:147860317 | C | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+15110C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147860317 | |||||||
| chr2:147860680 | A | G | 2 | a0001c0001t0002g0245 a0001c0001t0002g0246 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.55+15473A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147860680 | |||||||
| chr2:147860698 | T | C | 276 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.55+15491T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147860698 | |||||||
| chr2:147860979 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.55+15772A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147860979 | |||||||
| chr2:147861068 | A | G | 5 | a0001c0001t0001g0190 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG01167.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+15861A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147861068 | |||||||
| chr2:147861185 | A | G | 101 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0114 others(98): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.55+15978A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147861185 | |||||||
| chr2:147861245 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.55+16038T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147861245 | |||||||
| chr2:147861836 | A | G | 1 | a0001c0001t0003g0294 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.55+16629A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147861836 | |||||||
| chr2:147861904 | T | TGTTTTAT others(310): Show |
1 | a0001c0002t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55+16709_55+16710i others(319): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147861904 | ||||||
| chr2:147861904 | T | TGTTTTAT others(311): Show |
1 | a0001c0002t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55+16709_55+16710i others(320): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147861904 | ||||||
| chr2:147861904 | T | TGTTTTAT others(310): Show |
2 | a0001c0002t0001g0051 a0001c0002t0009g0172 |
2 | HG02109.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.55+16712_55+16713i others(319): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147861904 | ||||||
| chr2:147861904 | T | TGTTTTAT others(311): Show |
10 | a0001c0001t0001g0094 a0001c0002t0001g0026 a0001c0002t0001g0027 others(7): Show |
10 | HG00738.hp1 HG01123.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.55+16712_55+16713i others(320): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147861904 | ||||||
| chr2:147861904 | T | TGTTTTAT others(312): Show |
13 | a0001c0002t0001g0025 a0001c0002t0001g0028 a0001c0002t0001g0029 others(10): Show |
13 | HG00423.hp1 HG01175.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.55+16712_55+16713i others(321): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147861904 | ||||||
| chr2:147862031 | A | G | 1 | a0001c0002t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.55+16824A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862031 | |||||||
| chr2:147862177 | T | C | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.55+16970T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862177 | |||||||
| chr2:147862261 | C | T | 1 | a0001c0002t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55+17054C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862261 | |||||||
| chr2:147862264 | A | G | 1 | a0001c0002t0001g0141 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.55+17057A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862264 | |||||||
| chr2:147862313 | T | G | 1 | a0001c0002t0011g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.55+17106T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862313 | |||||||
| chr2:147862369 | A | AT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
7 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+17165dupT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147862369 | ||||||
| chr2:147862373 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
7 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+17166G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862373 | |||||||
| chr2:147862607 | G | T | 1 | a0001c0002t0012g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.55+17400G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862607 | |||||||
| chr2:147862608 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.55+17401G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862608 | |||||||
| chr2:147862692 | C | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.55+17485C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862692 | |||||||
| chr2:147862693 | G | C | 1 | a0001c0001t0002g0150 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.55+17486G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862693 | |||||||
| chr2:147862743 | C | CA | 91 | a0001c0001t0001g0282 a0001c0002t0001g0004 a0001c0002t0001g0005 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.55+17549dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147862743 | ||||||
| chr2:147862979 | G | C | 2 | a0001c0001t0003g0299 a0001c0001t0003g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.55+17772G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147862979 | |||||||
| chr2:147863079 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0189 a0001c0001t0001g0256 others(10): Show |
14 | HG00099.hp1 HG00408.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.55+17872T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147863079 | |||||||
| chr2:147863431 | A | G | 24 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.55+18224A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147863431 | |||||||
| chr2:147863578 | T | G | 1 | a0001c0002t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55+18371T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147863578 | |||||||
| chr2:147864206 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+18999A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864206 | |||||||
| chr2:147864261 | A | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.55+19054A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864261 | |||||||
| chr2:147864292 | C | T | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | NA18981.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.55+19085C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864292 | |||||||
| chr2:147864392 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0192 a0001c0001t0001g0193 |
4 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+19185G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864392 | |||||||
| chr2:147864508 | G | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+19301G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864508 | |||||||
| chr2:147864520 | G | A | 1 | a0001c0001t0003g0301 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.55+19313G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864520 | |||||||
| chr2:147864695 | G | C | 4 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(1): Show |
4 | HG02622.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+19488G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864695 | |||||||
| chr2:147864750 | A | T | 2 | a0001c0002t0011g0112 a0001c0002t0012g0144 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.55+19543A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147864750 | |||||||
| chr2:147865013 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.55+19806C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865013 | |||||||
| chr2:147865408 | T | G | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.55+20201T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865408 | |||||||
| chr2:147865480 | T | C | 2 | a0001c0002t0001g0119 a0001c0002t0001g0120 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.55+20273T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865480 | |||||||
| chr2:147865550 | C | T | 27 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(24): Show |
27 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.55+20343C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865550 | |||||||
| chr2:147865729 | A | G | 1 | a0001c0002t0011g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.55+20522A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865729 | |||||||
| chr2:147865735 | C | T | 101 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0114 others(98): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.55+20528C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865735 | |||||||
| chr2:147865766 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.55+20559A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865766 | |||||||
| chr2:147865884 | T | G | 128 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(125): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.55+20677T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865884 | |||||||
| chr2:147865914 | C | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+20707C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865914 | |||||||
| chr2:147865915 | T | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+20708T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147865915 | |||||||
| chr2:147866001 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0184 others(1): Show |
4 | HG00639.hp1 HG02886.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+20794G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147866001 | |||||||
| chr2:147866265 | A | G | 27 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(24): Show |
27 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.55+21058A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147866265 | |||||||
| chr2:147866344 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+21137C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147866344 | |||||||
| chr2:147866416 | C | T | 3 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 |
3 | NA18946.hp1 NA18965.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.55+21209C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147866416 | |||||||
| chr2:147866930 | C | G | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.55+21723C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147866930 | |||||||
| chr2:147867016 | G | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+21809G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867016 | |||||||
| chr2:147867458 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.55+22251C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867458 | |||||||
| chr2:147867475 | C | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+22268C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867475 | |||||||
| chr2:147867478 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.55+22271G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867478 | |||||||
| chr2:147867622 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+22415A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867622 | |||||||
| chr2:147867813 | C | G | 3 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 |
3 | HG00280.hp2 HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.55+22606C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867813 | |||||||
| chr2:147867826 | C | T | 1 | a0001c0002t0001g0030 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.55+22619C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867826 | |||||||
| chr2:147867933 | A | G | 3 | a0001c0002t0001g0045 a0001c0002t0001g0081 a0001c0002t0001g0109 |
3 | HG01070.hp1 HG01884.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.55+22726A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867933 | |||||||
| chr2:147867994 | T | C | 24 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.55+22787T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147867994 | |||||||
| chr2:147868179 | G | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+22972G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868179 | |||||||
| chr2:147868257 | G | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+23050G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868257 | |||||||
| chr2:147868291 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55+23084G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868291 | |||||||
| chr2:147868305 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.55+23098A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868305 | |||||||
| chr2:147868352 | A | G | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(3): Show |
6 | HG00408.hp1 HG03516.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+23145A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868352 | |||||||
| chr2:147868453 | C | A | 299 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(296): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.55+23246C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868453 | |||||||
| chr2:147868571 | T | C | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.55+23364T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868571 | |||||||
| chr2:147868621 | T | TTTATTTA others(8): Show |
5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+23416_55+23417i others(17): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147868621 | ||||||
| chr2:147868621 | T | TTTTATTT others(5): Show |
1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+23431_55+23442d others(14): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147868621 | ||||||
| chr2:147868860 | A | T | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(3): Show |
6 | HG00408.hp1 HG03516.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+23653A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147868860 | |||||||
| chr2:147869030 | A | G | 1 | a0001c0002t0012g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.55+23823A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869030 | |||||||
| chr2:147869125 | T | C | 1 | a0001c0001t0002g0206 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.55+23918T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869125 | |||||||
| chr2:147869127 | C | A | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.55+23920C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869127 | |||||||
| chr2:147869155 | G | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+23948G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869155 | |||||||
| chr2:147869364 | TGCTTATT others(1): Show |
T | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.55+24158_55+24165d others(10): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869364 | |||||||
| chr2:147869425 | C | A | 2 | a0001c0001t0002g0151 a0001c0001t0002g0207 |
2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.55+24218C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869425 | |||||||
| chr2:147869704 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.55+24497A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869704 | |||||||
| chr2:147869827 | C | T | 30 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(27): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.55+24620C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869827 | |||||||
| chr2:147869917 | AGTATGTT others(6): Show |
A | 1 | a0001c0002t0001g0090 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.55+24714_55+24726d others(15): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147869917 | ||||||
| chr2:147869959 | C | A | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.55+24752C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147869959 | |||||||
| chr2:147870072 | G | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.55+24865G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870072 | |||||||
| chr2:147870127 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.55+24920G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870127 | |||||||
| chr2:147870434 | C | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.55+25227C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870434 | |||||||
| chr2:147870481 | T | G | 30 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(27): Show |
39 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.55+25274T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870481 | |||||||
| chr2:147870593 | G | A | 298 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(295): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.55+25386G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870593 | |||||||
| chr2:147870790 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.56-25511C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870790 | |||||||
| chr2:147870816 | A | G | 1 | a0001c0001t0003g0293 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.56-25485A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870816 | |||||||
| chr2:147870866 | C | T | 1 | a0001c0002t0001g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.56-25435C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147870866 | |||||||
| chr2:147870904 | TTTAA | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
7 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-25391_56-25388d others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147870904 | ||||||
| chr2:147871041 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(1): Show |
4 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-25260C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871041 | |||||||
| chr2:147871065 | A | G | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.56-25236A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871065 | |||||||
| chr2:147871403 | C | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-24898C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871403 | |||||||
| chr2:147871413 | A | T | 1 | a0001c0002t0001g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-24888A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871413 | |||||||
| chr2:147871480 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0183 |
2 | HG00639.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.56-24821A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871480 | |||||||
| chr2:147871492 | G | T | 1 | a0001c0002t0001g0056 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.56-24809G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871492 | |||||||
| chr2:147871621 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56-24680G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871621 | |||||||
| chr2:147871728 | G | A | 1 | a0001c0001t0003g0293 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.56-24573G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871728 | |||||||
| chr2:147871775 | C | G | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56-24526C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147871775 | |||||||
| chr2:147872050 | C | A | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56-24251C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147872050 | |||||||
| chr2:147872315 | A | G | 1 | a0001c0002t0011g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.56-23986A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147872315 | |||||||
| chr2:147872563 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0189 a0001c0001t0001g0256 others(4): Show |
8 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.56-23738C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147872563 | |||||||
| chr2:147872770 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.56-23531A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147872770 | |||||||
| chr2:147872821 | C | G | 1 | a0001c0001t0002g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.56-23480C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147872821 | |||||||
| chr2:147873012 | C | T | 6 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-23289C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873012 | |||||||
| chr2:147873172 | G | C | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.56-23129G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873172 | |||||||
| chr2:147873236 | A | G | 1 | a0001c0002t0013g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.56-23065A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873236 | |||||||
| chr2:147873302 | T | G | 4 | a0001c0002t0001g0035 a0001c0002t0001g0064 a0001c0002t0001g0110 others(1): Show |
4 | NA18948.hp2 NA18974.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-22999T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873302 | |||||||
| chr2:147873408 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-22893C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873408 | |||||||
| chr2:147873511 | A | C | 1 | a0001c0001t0002g0239 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.56-22790A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873511 | |||||||
| chr2:147873660 | GAGAC | G | 32 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(29): Show |
41 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.56-22637_56-22634d others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147873660 | ||||||
| chr2:147873663 | A | T | 137 | a0001c0001t0001g0094 a0001c0001t0003g0188 a0001c0001t0003g0280 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.56-22638A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873663 | |||||||
| chr2:147873705 | A | T | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.56-22596A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873705 | |||||||
| chr2:147873735 | T | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-22566T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873735 | |||||||
| chr2:147873864 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0148 a0001c0001t0001g0278 others(2): Show |
6 | HG00735.hp2 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-22437G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873864 | |||||||
| chr2:147873966 | G | A | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.56-22335G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873966 | |||||||
| chr2:147873967 | C | T | 5 | a0001c0001t0001g0190 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG01167.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-22334C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873967 | |||||||
| chr2:147873985 | T | A | 4 | a0001c0002t0001g0030 a0001c0002t0001g0057 a0001c0002t0001g0095 others(1): Show |
4 | HG01943.hp1 NA18971.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-22316T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147873985 | |||||||
| chr2:147874214 | C | G | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.56-22087C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147874214 | |||||||
| chr2:147874650 | A | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.56-21651A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147874650 | |||||||
| chr2:147874799 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.56-21502C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147874799 | |||||||
| chr2:147874959 | A | T | 1 | a0001c0008t0004g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.56-21342A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147874959 | |||||||
| chr2:147874982 | C | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0200 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.56-21319C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147874982 | |||||||
| chr2:147875323 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.56-20978A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875323 | |||||||
| chr2:147875374 | G | A | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(3): Show |
6 | HG00408.hp1 HG03516.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-20927G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875374 | |||||||
| chr2:147875385 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0189 a0001c0001t0001g0256 others(4): Show |
8 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.56-20916C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875385 | |||||||
| chr2:147875427 | C | T | 1 | a0001c0002t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-20874C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875427 | |||||||
| chr2:147875494 | T | TA | 24 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.56-20800dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147875494 | ||||||
| chr2:147875607 | G | T | 1 | a0001c0002t0001g0080 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.56-20694G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875607 | |||||||
| chr2:147875681 | A | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-20620A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875681 | |||||||
| chr2:147875715 | A | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-20586A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875715 | |||||||
| chr2:147875942 | G | C | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56-20359G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147875942 | |||||||
| chr2:147876022 | C | T | 2 | a0001c0001t0002g0164 a0001c0001t0002g0168 |
2 | NA19085.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.56-20279C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147876022 | |||||||
| chr2:147876065 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.56-20236T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147876065 | |||||||
| chr2:147876341 | A | T | 2 | a0001c0004t0001g0261 a0001c0004t0001g0262 |
2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.56-19960A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147876341 | |||||||
| chr2:147876367 | A | C | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.56-19934A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147876367 | |||||||
| chr2:147876409 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0018g0014 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.56-19892G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147876409 | |||||||
| chr2:147876599 | A | T | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.56-19702A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147876599 | |||||||
| chr2:147876923 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.56-19378C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147876923 | |||||||
| chr2:147877039 | C | CAT | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.56-19262_56-19261i others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877039 | |||||||
| chr2:147877117 | G | T | 1 | a0001c0002t0001g0054 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.56-19184G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877117 | |||||||
| chr2:147877139 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-19162C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877139 | |||||||
| chr2:147877199 | C | G | 18 | a0001c0001t0002g0015 a0001c0001t0002g0019 a0001c0001t0002g0160 others(15): Show |
20 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-19102C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877199 | |||||||
| chr2:147877382 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.56-18919G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877382 | |||||||
| chr2:147877390 | C | T | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.56-18911C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877390 | |||||||
| chr2:147877582 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56-18719A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877582 | |||||||
| chr2:147877659 | A | G | 276 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.56-18642A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877659 | |||||||
| chr2:147877884 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0229 |
2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.56-18417A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877884 | |||||||
| chr2:147877917 | C | T | 2 | a0001c0002t0001g0097 a0001c0002t0001g0099 |
2 | NA18984.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.56-18384C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877917 | |||||||
| chr2:147877968 | A | G | 2 | a0001c0002t0001g0033 a0001c0002t0001g0034 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.56-18333A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147877968 | |||||||
| chr2:147878224 | A | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-18077A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147878224 | |||||||
| chr2:147878319 | A | G | 1 | a0001c0002t0012g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.56-17982A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147878319 | |||||||
| chr2:147878348 | A | G | 2 | a0001c0001t0003g0292 a0001c0001t0003g0297 |
2 | NA18946.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.56-17953A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147878348 | |||||||
| chr2:147878444 | C | CT | 33 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(30): Show |
42 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.56-17845dupT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147878444 | ||||||
| chr2:147878472 | A | G | 24 | a0001c0001t0001g0094 a0001c0002t0001g0025 a0001c0002t0001g0026 others(21): Show |
24 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.56-17829A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147878472 | |||||||
| chr2:147878564 | G | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-17737G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147878564 | |||||||
| chr2:147878908 | TA | T | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.56-17382delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147878908 | ||||||
| chr2:147878937 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.56-17364A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147878937 | |||||||
| chr2:147878987 | G | T | 298 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(295): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.56-17314G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147878987 | |||||||
| chr2:147879018 | C | A | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56-17283C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879018 | |||||||
| chr2:147879048 | T | G | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-17253T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879048 | |||||||
| chr2:147879247 | T | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-17054T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879247 | |||||||
| chr2:147879248 | C | T | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-17053C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879248 | |||||||
| chr2:147879424 | C | T | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.56-16877C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879424 | |||||||
| chr2:147879508 | A | T | 276 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.56-16793A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879508 | |||||||
| chr2:147879552 | G | C | 1 | a0001c0001t0002g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.56-16749G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879552 | |||||||
| chr2:147879565 | A | T | 1 | a0001c0001t0002g0151 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.56-16736A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879565 | |||||||
| chr2:147879660 | A | G | 1 | a0001c0001t0016g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.56-16641A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879660 | |||||||
| chr2:147879661 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.56-16640G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879661 | |||||||
| chr2:147879798 | G | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-16503G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879798 | |||||||
| chr2:147879893 | A | C | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.56-16408A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879893 | |||||||
| chr2:147879922 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.56-16379G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147879922 | |||||||
| chr2:147880075 | T | C | 1 | a0001c0002t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-16226T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147880075 | |||||||
| chr2:147880218 | A | T | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-16083A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147880218 | |||||||
| chr2:147880726 | T | C | 1 | a0001c0002t0011g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.56-15575T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147880726 | |||||||
| chr2:147881325 | T | C | 1 | a0001c0001t0003g0295 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.56-14976T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147881325 | |||||||
| chr2:147881525 | T | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-14776T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147881525 | |||||||
| chr2:147881601 | T | G | 2 | a0001c0001t0004g0022 a0001c0001t0004g0123 |
2 | HG00408.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.56-14700T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147881601 | |||||||
| chr2:147881601 | TAGTGTGT others(5): Show |
T | 2 | a0001c0001t0002g0196 a0001c0002t0001g0113 |
2 | HG03471.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.56-14699_56-14688d others(14): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147881601 | |||||||
| chr2:147881602 | A | AGT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0192 a0001c0001t0001g0200 others(6): Show |
9 | HG02027.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-14660_56-14659d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881602 | ||||||
| chr2:147881602 | A | AGTGT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG01884.hp2 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-14662_56-14659d others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881602 | ||||||
| chr2:147881602 | A | AGTGTGT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0256 others(6): Show |
10 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.56-14664_56-14659d others(8): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881602 | ||||||
| chr2:147881602 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.56-14668_56-14659d others(12): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881602 | ||||||
| chr2:147881602 | A | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0123 |
2 | HG00408.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.56-14699A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147881602 | |||||||
| chr2:147881602 | AGT | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0001g0257 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-14660_56-14659d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881602 | ||||||
| chr2:147881602 | AGTGTGTG others(1): Show |
A | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
42 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.56-14666_56-14659d others(10): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881602 | ||||||
| chr2:147881602 | AGTGTGTG others(5): Show |
A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0003g0003 |
3 | HG00639.hp2 HG01358.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.56-14670_56-14659d others(14): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881602 | ||||||
| chr2:147881619 | GTGTGTGT others(17): Show |
G | 1 | a0001c0002t0001g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.56-14663_56-14640d others(26): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881619 | ||||||
| chr2:147881621 | GTGTGTGT others(15): Show |
G | 4 | a0001c0002t0001g0064 a0001c0002t0001g0110 a0001c0002t0009g0172 others(1): Show |
4 | HG02109.hp1 NA18948.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-14661_56-14640d others(24): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881621 | ||||||
| chr2:147881625 | GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0002g0217 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.56-14658_56-14641d others(20): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881625 | ||||||
| chr2:147881629 | GTGTGTGT others(7): Show |
G | 7 | a0001c0001t0002g0161 a0001c0001t0002g0205 a0001c0001t0002g0216 others(4): Show |
7 | HG01975.hp2 HG02622.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-14658_56-14645d others(16): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881629 | ||||||
| chr2:147881631 | GTGTGTGT others(5): Show |
G | 32 | a0001c0001t0001g0094 a0001c0001t0001g0114 a0001c0001t0001g0229 others(29): Show |
32 | HG00423.hp1 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.56-14658_56-14647d others(14): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881631 | ||||||
| chr2:147881633 | GTGTGTGT others(3): Show |
G | 55 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0148 others(52): Show |
58 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.56-14658_56-14649d others(12): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881633 | ||||||
| chr2:147881635 | GTGTGTGT others(1): Show |
G | 40 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0002g0001 others(37): Show |
41 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.56-14658_56-14651d others(10): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881635 | ||||||
| chr2:147881637 | GTGTGTA | G | 39 | a0001c0001t0001g0146 a0001c0001t0001g0199 a0001c0001t0002g0015 others(36): Show |
40 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.56-14658_56-14653d others(8): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881637 | ||||||
| chr2:147881639 | GTGTA | G | 24 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0001g0198 others(21): Show |
24 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.56-14658_56-14655d others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881639 | ||||||
| chr2:147881641 | GTA | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0178 a0001c0001t0001g0184 others(19): Show |
23 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-14658_56-14657d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881641 | ||||||
| chr2:147881643 | A | G | 30 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
32 | HG00408.hp1 HG01070.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.56-14658A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147881643 | |||||||
| chr2:147881648 | TGTGTGTG others(6): Show |
T | 1 | a0001c0001t0002g0159 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.56-14650_56-14638d others(15): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147881648 | ||||||
| chr2:147881923 | G | A | 7 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0198 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-14378G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147881923 | |||||||
| chr2:147882207 | A | G | 3 | a0001c0001t0001g0178 a0001c0001t0002g0151 a0001c0001t0002g0207 |
3 | HG00639.hp1 HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.56-14094A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147882207 | |||||||
| chr2:147882269 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56-14032C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147882269 | |||||||
| chr2:147882437 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56-13864G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147882437 | |||||||
| chr2:147882539 | G | A | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.56-13762G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147882539 | |||||||
| chr2:147882806 | C | T | 1 | a0001c0001t0002g0239 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.56-13495C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147882806 | |||||||
| chr2:147882810 | CAA | C | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.56-13490_56-13489d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147882810 | |||||||
| chr2:147882816 | GA | G | 4 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(1): Show |
4 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-13477delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147882816 | ||||||
| chr2:147882840 | C | T | 1 | a0001c0002t0001g0121 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.56-13461C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147882840 | |||||||
| chr2:147883023 | G | A | 1 | a0001c0001t0006g0187 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.56-13278G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147883023 | |||||||
| chr2:147883199 | T | C | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.56-13102T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147883199 | |||||||
| chr2:147883361 | T | C | 95 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(92): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.56-12940T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147883361 | |||||||
| chr2:147883944 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.56-12357A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147883944 | |||||||
| chr2:147883998 | T | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0278 a0001c0001t0001g0279 |
4 | HG00735.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.56-12303T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147883998 | |||||||
| chr2:147884240 | T | C | 112 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.56-12061T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147884240 | |||||||
| chr2:147884244 | C | T | 1 | a0001c0002t0001g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.56-12057C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147884244 | |||||||
| chr2:147884321 | G | C | 1 | a0001c0001t0002g0205 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.56-11980G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147884321 | |||||||
| chr2:147884538 | C | G | 1 | a0001c0001t0002g0253 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.56-11763C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147884538 | |||||||
| chr2:147884644 | C | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-11657C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147884644 | |||||||
| chr2:147884703 | A | G | 2 | a0001c0001t0006g0187 a0001c0001t0006g0283 |
2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.56-11598A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147884703 | |||||||
| chr2:147884829 | T | A | 1 | a0001c0002t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-11472T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147884829 | |||||||
| chr2:147885255 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.56-11046C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885255 | |||||||
| chr2:147885309 | G | C | 7 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(4): Show |
7 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-10992G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885309 | |||||||
| chr2:147885549 | C | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.56-10752C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885549 | |||||||
| chr2:147885647 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56-10654G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885647 | |||||||
| chr2:147885690 | A | C | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.56-10611A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885690 | |||||||
| chr2:147885735 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.56-10566A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885735 | |||||||
| chr2:147885818 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0018g0014 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.56-10483A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885818 | |||||||
| chr2:147885986 | T | C | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.56-10315T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147885986 | |||||||
| chr2:147886197 | A | G | 2 | a0001c0001t0003g0291 a0001c0001t0003g0294 |
2 | HG02165.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.56-10104A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147886197 | |||||||
| chr2:147886288 | G | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-10013G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147886288 | |||||||
| chr2:147886387 | A | G | 9 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0043 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-9914A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147886387 | |||||||
| chr2:147886410 | A | G | 7 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(4): Show |
7 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-9891A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147886410 | |||||||
| chr2:147886554 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.56-9747C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147886554 | |||||||
| chr2:147886612 | A | G | 1 | a0001c0001t0003g0273 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.56-9689A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147886612 | |||||||
| chr2:147886771 | C | CT | 29 | a0001c0001t0002g0158 a0001c0001t0002g0195 a0001c0001t0002g0197 others(26): Show |
29 | HG00423.hp1 HG00609.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.56-9514dupT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147886771 | ||||||
| chr2:147886771 | CT | C | 7 | a0001c0001t0001g0260 a0001c0001t0002g0160 a0001c0001t0002g0230 others(4): Show |
7 | HG01071.hp2 HG01168.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-9514delT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147886771 | ||||||
| chr2:147886915 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.56-9386T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147886915 | |||||||
| chr2:147887211 | C | CA | 10 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(7): Show |
12 | HG01243.hp2 HG02145.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.56-9076dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147887211 | ||||||
| chr2:147887211 | CA | C | 11 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
12 | HG00639.hp1 HG01167.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.56-9076delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147887211 | ||||||
| chr2:147887362 | T | A | 1 | a0001c0001t0003g0270 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.56-8939T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147887362 | |||||||
| chr2:147887668 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.56-8633G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147887668 | |||||||
| chr2:147887758 | A | G | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.56-8543A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147887758 | |||||||
| chr2:147888050 | C | T | 1 | a0001c0002t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.56-8251C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888050 | |||||||
| chr2:147888089 | A | G | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.56-8212A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888089 | |||||||
| chr2:147888210 | T | A | 1 | a0001c0002t0011g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.56-8091T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888210 | |||||||
| chr2:147888301 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.56-8000A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888301 | |||||||
| chr2:147888401 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-7900A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888401 | |||||||
| chr2:147888533 | A | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-7768A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888533 | |||||||
| chr2:147888538 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56-7763C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888538 | |||||||
| chr2:147888544 | C | G | 1 | a0001c0002t0001g0137 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.56-7757C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888544 | |||||||
| chr2:147888590 | A | G | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-7711A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888590 | |||||||
| chr2:147888618 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-7683C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888618 | |||||||
| chr2:147888627 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.56-7674A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888627 | |||||||
| chr2:147888633 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.56-7668T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888633 | |||||||
| chr2:147888664 | G | GGCT | 23 | a0001c0001t0003g0003 a0001c0001t0003g0020 a0001c0001t0003g0188 others(20): Show |
27 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.56-7624_56-7622dup others(3): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147888664 | ||||||
| chr2:147888680 | T | G | 12 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0272 others(9): Show |
17 | NA18612.hp2 NA18941.hp1 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.56-7621T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888680 | |||||||
| chr2:147888681 | C | CTTCT | 8 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0272 others(5): Show |
13 | NA18943.hp1 NA18946.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-7618_56-7617ins others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147888681 | ||||||
| chr2:147888681 | CT | C | 6 | a0001c0001t0002g0015 a0001c0002t0001g0026 a0001c0002t0001g0102 others(3): Show |
7 | HG00099.hp2 HG01975.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-7604delT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147888681 | ||||||
| chr2:147888806 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-7495A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888806 | |||||||
| chr2:147888861 | G | A | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.56-7440G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147888861 | |||||||
| chr2:147889022 | A | G | 306 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(303): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.56-7279A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147889022 | |||||||
| chr2:147889173 | G | A | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.56-7128G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147889173 | |||||||
| chr2:147889382 | CAT | C | 6 | a0001c0002t0001g0023 a0001c0002t0001g0039 a0001c0002t0001g0075 others(3): Show |
6 | HG00438.hp2 NA18943.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-6918_56-6917del others(2): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147889382 | |||||||
| chr2:147889467 | G | A | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02895.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.56-6834G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147889467 | |||||||
| chr2:147889863 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.56-6438C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147889863 | |||||||
| chr2:147889900 | T | G | 1 | a0001c0001t0002g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.56-6401T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147889900 | |||||||
| chr2:147889942 | G | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0127 |
2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.56-6359G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147889942 | |||||||
| chr2:147890341 | A | AGT | 12 | a0001c0001t0001g0148 a0001c0001t0001g0267 a0001c0001t0001g0281 others(9): Show |
12 | HG00741.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.56-5933_56-5932dup others(2): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147890341 | ||||||
| chr2:147890341 | A | AGTGT | 105 | a0001c0001t0001g0094 a0001c0001t0001g0173 a0001c0001t0001g0174 others(102): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.56-5935_56-5932dup others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147890341 | ||||||
| chr2:147890341 | A | AGTGTGT | 35 | a0001c0001t0001g0189 a0001c0001t0001g0256 a0001c0001t0002g0147 others(32): Show |
35 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.56-5937_56-5932dup others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147890341 | ||||||
| chr2:147890341 | A | AGTGTGTG others(1): Show |
78 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(75): Show |
84 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.56-5939_56-5932dup others(8): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147890341 | ||||||
| chr2:147890341 | A | AGTGTGTG others(3): Show |
13 | a0001c0001t0001g0114 a0001c0001t0001g0229 a0001c0001t0002g0149 others(10): Show |
13 | HG00438.hp1 HG00738.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-5941_56-5932dup others(10): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147890341 | ||||||
| chr2:147890341 | A | AGTGTGTG others(5): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0146 others(2): Show |
7 | HG02145.hp1 HG02602.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-5943_56-5932dup others(12): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147890341 | ||||||
| chr2:147890341 | AGT | A | 34 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0003g0002 others(31): Show |
43 | HG00609.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.56-5933_56-5932del others(2): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147890341 | ||||||
| chr2:147890370 | A | G | 4 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
4 | HG00609.hp2 NA18945.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-5931A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147890370 | |||||||
| chr2:147890411 | A | C | 2 | a0001c0001t0016g0162 a0001c0001t0017g0167 |
2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.56-5890A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147890411 | |||||||
| chr2:147890432 | A | T | 32 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(29): Show |
41 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.56-5869A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147890432 | |||||||
| chr2:147890490 | A | G | 91 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.56-5811A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147890490 | |||||||
| chr2:147890703 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56-5598G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147890703 | |||||||
| chr2:147890793 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-5508A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147890793 | |||||||
| chr2:147890917 | C | T | 129 | a0001c0001t0001g0094 a0001c0002t0001g0004 a0001c0002t0001g0005 others(126): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.56-5384C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147890917 | |||||||
| chr2:147891248 | TG | T | 3 | a0001c0001t0002g0154 a0001c0001t0002g0208 a0001c0001t0002g0215 |
3 | NA18975.hp1 NA18978.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.56-5052delG | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147891248 | |||||||
| chr2:147891606 | T | G | 6 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.56-4695T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147891606 | |||||||
| chr2:147891817 | G | A | 134 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(131): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.56-4484G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147891817 | |||||||
| chr2:147891919 | T | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-4382T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147891919 | |||||||
| chr2:147891958 | TTTTTGTT others(12): Show |
T | 1 | a0001c0001t0002g0216 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.56-4330_56-4312del others(19): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147891958 | ||||||
| chr2:147891962 | T | TG | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.56-4338dupG | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147891962 | ||||||
| chr2:147892068 | T | C | 1 | a0001c0001t0003g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.56-4233T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892068 | |||||||
| chr2:147892071 | A | G | 2 | a0001c0002t0001g0074 a0001c0002t0001g0136 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.56-4230A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892071 | |||||||
| chr2:147892099 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56-4202G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892099 | |||||||
| chr2:147892284 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG00735.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.56-4017C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892284 | |||||||
| chr2:147892434 | C | T | 2 | a0001c0001t0003g0188 a0001c0001t0003g0280 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.56-3867C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892434 | |||||||
| chr2:147892494 | A | AAACTTTT others(283): Show |
1 | a0001c0002t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.56-3798_56-3797ins others(290): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892494 | A | AAACTTTT others(296): Show |
6 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0118 others(3): Show |
6 | HG02886.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-3798_56-3797ins others(303): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892494 | A | AAACTTTT others(296): Show |
3 | a0001c0002t0001g0068 a0001c0002t0001g0102 a0001c0002t0001g0126 |
3 | HG00323.hp1 NA18957.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.56-3798_56-3797ins others(303): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892494 | A | AAACTTTT others(297): Show |
54 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0007 others(51): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.56-3798_56-3797ins others(304): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892494 | A | AAACTTTT others(298): Show |
34 | a0001c0002t0001g0006 a0001c0002t0001g0030 a0001c0002t0001g0032 others(31): Show |
36 | HG00735.hp1 HG01123.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.56-3798_56-3797ins others(305): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892494 | A | AAACTTTT others(299): Show |
16 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0028 others(13): Show |
16 | HG00280.hp1 HG00738.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.56-3798_56-3797ins others(306): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892494 | A | AAACTTTT others(300): Show |
7 | a0001c0002t0001g0027 a0001c0002t0001g0029 a0001c0002t0001g0053 others(4): Show |
7 | HG00423.hp1 HG01175.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-3798_56-3797ins others(307): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892494 | A | AAACTTTT others(301): Show |
1 | a0001c0002t0001g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.56-3798_56-3797ins others(308): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892494 | ||||||
| chr2:147892503 | T | TTTTTTTT others(297): Show |
5 | a0001c0002t0001g0024 a0001c0002t0001g0130 a0001c0002t0001g0131 others(2): Show |
5 | NA18944.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-3798_56-3797ins others(304): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892503 | |||||||
| chr2:147892503 | T | TTTTTTTT others(298): Show |
1 | a0001c0002t0001g0133 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.56-3798_56-3797ins others(305): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892503 | |||||||
| chr2:147892620 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-3681A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892620 | |||||||
| chr2:147892782 | A | G | 1 | a0001c0001t0003g0301 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.56-3519A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892782 | |||||||
| chr2:147892888 | G | GT | 7 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.56-3405dupT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147892888 | ||||||
| chr2:147892904 | G | A | 134 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(131): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.56-3397G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147892904 | |||||||
| chr2:147893004 | C | A | 1 | a0001c0002t0001g0101 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.56-3297C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893004 | |||||||
| chr2:147893149 | G | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.56-3152G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893149 | |||||||
| chr2:147893240 | A | AT | 23 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(20): Show |
23 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.56-3059dupT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147893240 | ||||||
| chr2:147893297 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.56-3004G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893297 | |||||||
| chr2:147893468 | AC | A | 102 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0094 others(99): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.56-2832delC | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893468 | |||||||
| chr2:147893635 | A | G | 2 | a0001c0002t0001g0119 a0001c0002t0001g0120 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.56-2666A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893635 | |||||||
| chr2:147893723 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.56-2578C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893723 | |||||||
| chr2:147893806 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.56-2495T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893806 | |||||||
| chr2:147893889 | G | A | 284 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(281): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.56-2412G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147893889 | |||||||
| chr2:147894054 | G | A | 1 | a0001c0001t0003g0285 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.56-2247G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894054 | |||||||
| chr2:147894220 | G | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-2081G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894220 | |||||||
| chr2:147894426 | CT | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-1870delT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 147894426 | ||||||
| chr2:147894438 | T | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | NA18981.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.56-1863T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894438 | |||||||
| chr2:147894490 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.56-1811C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894490 | |||||||
| chr2:147894596 | C | T | 1 | a0001c0001t0003g0290 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.56-1705C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894596 | |||||||
| chr2:147894616 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.56-1685C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894616 | |||||||
| chr2:147894643 | T | C | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-1658T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894643 | |||||||
| chr2:147894800 | G | C | 4 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0077 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-1501G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147894800 | |||||||
| chr2:147895130 | C | G | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.56-1171C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147895130 | |||||||
| chr2:147895292 | T | G | 1 | a0001c0001t0002g0019 | 2 | NA18941.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.56-1009T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147895292 | |||||||
| chr2:147895317 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-984C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147895317 | |||||||
| chr2:147895586 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-715A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147895586 | |||||||
| chr2:147895904 | CCTT | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.56-396_56-394delCT others(1): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147895904 | |||||||
| chr2:147895961 | G | C | 1 | a0001c0001t0002g0217 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.56-340G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 1/10 | chr2 | 147895961 | |||||||
| chr2:147896613 | T | A | 1 | a0001c0001t0003g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.263+105T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147896613 | |||||||
| chr2:147896780 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.263+272C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147896780 | |||||||
| chr2:147896909 | T | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+401T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147896909 | |||||||
| chr2:147896997 | G | A | 1 | a0001c0001t0003g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.263+489G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147896997 | |||||||
| chr2:147897097 | C | T | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.263+589C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897097 | |||||||
| chr2:147897197 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+689A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897197 | |||||||
| chr2:147897228 | G | C | 1 | a0001c0002t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.263+720G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897228 | |||||||
| chr2:147897342 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.263+834T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897342 | |||||||
| chr2:147897372 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+864A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897372 | |||||||
| chr2:147897430 | G | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.263+922G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897430 | |||||||
| chr2:147897686 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.263+1178G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897686 | |||||||
| chr2:147897742 | C | T | 1 | a0001c0002t0001g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.263+1234C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147897742 | |||||||
| chr2:147898727 | T | A | 1 | a0001c0001t0003g0294 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.264-731T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147898727 | |||||||
| chr2:147898797 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.264-661A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147898797 | |||||||
| chr2:147899083 | A | G | 1 | a0001c0002t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.264-375A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147899083 | |||||||
| chr2:147899204 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.264-254A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 2/10 | chr2 | 147899204 | |||||||
| chr2:147899979 | A | T | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.528+81A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147899979 | |||||||
| chr2:147900020 | A | G | 136 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0094 others(133): Show |
151 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.528+122A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147900020 | |||||||
| chr2:147900227 | G | A | 26 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(23): Show |
26 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+329G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147900227 | |||||||
| chr2:147900277 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.528+379A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147900277 | |||||||
| chr2:147900559 | G | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+661G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147900559 | |||||||
| chr2:147900642 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.528+744G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147900642 | |||||||
| chr2:147900677 | C | G | 1 | a0001c0001t0002g0164 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.528+779C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147900677 | |||||||
| chr2:147901026 | G | A | 33 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(30): Show |
42 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.528+1128G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901026 | |||||||
| chr2:147901208 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.528+1310A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901208 | |||||||
| chr2:147901377 | T | C | 1 | a0001c0001t0003g0295 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.528+1479T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901377 | |||||||
| chr2:147901739 | T | C | 1 | a0001c0002t0001g0026 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.528+1841T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901739 | |||||||
| chr2:147901775 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0229 |
2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.528+1877A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901775 | |||||||
| chr2:147901790 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.528+1892G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901790 | |||||||
| chr2:147901837 | T | C | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(3): Show |
6 | HG00408.hp1 HG03516.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+1939T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901837 | |||||||
| chr2:147901898 | C | G | 23 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(20): Show |
23 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.528+2000C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147901898 | |||||||
| chr2:147902064 | C | T | 1 | a0001c0002t0001g0072 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.528+2166C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147902064 | |||||||
| chr2:147902341 | A | T | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.528+2443A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147902341 | |||||||
| chr2:147902819 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.528+2921G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147902819 | |||||||
| chr2:147903251 | G | GT | 12 | a0001c0001t0001g0016 a0001c0001t0001g0189 a0001c0001t0001g0256 others(9): Show |
13 | HG00099.hp1 HG00741.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+3365dupT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147903251 | ||||||
| chr2:147903365 | C | G | 1 | a0001c0002t0012g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.528+3467C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147903365 | |||||||
| chr2:147903474 | G | T | 283 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(280): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.528+3576G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147903474 | |||||||
| chr2:147903587 | T | C | 2 | a0001c0001t0006g0187 a0001c0001t0006g0283 |
2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.528+3689T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147903587 | |||||||
| chr2:147903610 | G | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+3712G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147903610 | |||||||
| chr2:147903933 | T | TA | 7 | a0001c0001t0001g0016 a0001c0001t0001g0189 a0001c0001t0001g0256 others(4): Show |
8 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+4036dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147903933 | ||||||
| chr2:147904003 | G | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+4105G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904003 | |||||||
| chr2:147904010 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.528+4112G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904010 | |||||||
| chr2:147904404 | C | G | 6 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+4506C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904404 | |||||||
| chr2:147904543 | G | C | 2 | a0001c0002t0001g0103 a0001c0002t0001g0106 |
2 | HG00544.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.528+4645G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904543 | |||||||
| chr2:147904559 | T | A | 1 | a0001c0001t0002g0251 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.528+4661T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904559 | |||||||
| chr2:147904633 | C | G | 23 | a0001c0002t0001g0031 a0001c0002t0001g0038 a0001c0002t0001g0041 others(20): Show |
24 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.528+4735C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904633 | |||||||
| chr2:147904736 | T | G | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528+4838T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904736 | |||||||
| chr2:147904810 | A | G | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.528+4912A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904810 | |||||||
| chr2:147904866 | A | G | 7 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(4): Show |
7 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+4968A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147904866 | |||||||
| chr2:147905013 | A | C | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.528+5115A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905013 | |||||||
| chr2:147905084 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.528+5186C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905084 | |||||||
| chr2:147905179 | A | G | 1 | a0001c0001t0003g0288 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.528+5281A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905179 | |||||||
| chr2:147905209 | A | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0235 a0001c0001t0002g0239 |
3 | HG00544.hp1 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.528+5311A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905209 | |||||||
| chr2:147905613 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+5715A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905613 | |||||||
| chr2:147905669 | A | G | 1 | a0001c0001t0003g0305 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.528+5771A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905669 | |||||||
| chr2:147905836 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.528+5938C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905836 | |||||||
| chr2:147905999 | G | T | 90 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(87): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.528+6101G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147905999 | |||||||
| chr2:147906294 | G | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.528+6396G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147906294 | |||||||
| chr2:147906606 | T | A | 1 | a0001c0001t0003g0296 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.528+6708T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147906606 | |||||||
| chr2:147906793 | G | C | 1 | a0001c0001t0001g0017 | 2 | HG00735.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.528+6895G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147906793 | |||||||
| chr2:147906818 | A | AT | 96 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0094 others(93): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.528+6941dupT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147906818 | ||||||
| chr2:147906818 | A | ATT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0257 others(5): Show |
9 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.528+6940_528+6941d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147906818 | ||||||
| chr2:147906818 | AT | A | 26 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(23): Show |
28 | HG00140.hp1 HG01069.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.528+6941delT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147906818 | ||||||
| chr2:147906818 | ATTTT | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+6938_528+6941d others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147906818 | ||||||
| chr2:147906840 | A | T | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(3): Show |
6 | HG00408.hp1 HG03516.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+6942A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147906840 | |||||||
| chr2:147907021 | C | A | 108 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.528+7123C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907021 | |||||||
| chr2:147907164 | A | T | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.528+7266A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907164 | |||||||
| chr2:147907166 | G | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.528+7268G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907166 | |||||||
| chr2:147907171 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+7273C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907171 | |||||||
| chr2:147907262 | C | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+7364C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907262 | |||||||
| chr2:147907636 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.529-7555T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907636 | |||||||
| chr2:147907947 | G | A | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529-7244G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907947 | |||||||
| chr2:147907988 | G | A | 91 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.529-7203G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147907988 | |||||||
| chr2:147908038 | C | CA | 11 | a0001c0001t0001g0016 a0001c0001t0001g0190 a0001c0001t0001g0256 others(8): Show |
12 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.529-7137dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147908038 | ||||||
| chr2:147908039 | AAAAAAAA others(9): Show |
A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-7143_529-7128d others(18): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147908039 | ||||||
| chr2:147908059 | AAAAAG | A | 29 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(26): Show |
38 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.529-7127_529-7123d others(7): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147908059 | ||||||
| chr2:147908060 | A | G | 1 | a0001c0001t0003g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.529-7131A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147908060 | |||||||
| chr2:147908064 | G | A | 1 | a0001c0001t0003g0289 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.529-7127G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147908064 | |||||||
| chr2:147908064 | G | GA | 7 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.529-7118dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147908064 | ||||||
| chr2:147908075 | C | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG00639.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.529-7116C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147908075 | |||||||
| chr2:147908204 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529-6987T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147908204 | |||||||
| chr2:147908206 | G | T | 1 | a0001c0001t0002g0204 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.529-6985G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147908206 | |||||||
| chr2:147908560 | T | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.529-6631T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147908560 | |||||||
| chr2:147908805 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.529-6386A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147908805 | |||||||
| chr2:147909154 | T | C | 305 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(302): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.529-6037T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909154 | |||||||
| chr2:147909175 | T | C | 287 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(284): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.529-6016T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909175 | |||||||
| chr2:147909192 | C | T | 91 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.529-5999C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909192 | |||||||
| chr2:147909224 | A | G | 1 | a0001c0002t0001g0134 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.529-5967A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909224 | |||||||
| chr2:147909254 | A | G | 1 | a0001c0002t0001g0026 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.529-5937A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909254 | |||||||
| chr2:147909266 | C | T | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.529-5925C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909266 | |||||||
| chr2:147909442 | T | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.529-5749T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909442 | |||||||
| chr2:147909551 | A | G | 3 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 |
3 | NA18946.hp1 NA18965.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.529-5640A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909551 | |||||||
| chr2:147909655 | G | A | 4 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(1): Show |
4 | HG02622.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-5536G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909655 | |||||||
| chr2:147909687 | G | A | 1 | a0001c0001t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.529-5504G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909687 | |||||||
| chr2:147909767 | A | G | 12 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(9): Show |
12 | HG00738.hp1 HG01175.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.529-5424A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909767 | |||||||
| chr2:147909794 | C | T | 1 | a0001c0001t0006g0283 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.529-5397C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909794 | |||||||
| chr2:147909815 | A | T | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-5376A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909815 | |||||||
| chr2:147909877 | A | G | 1 | a0001c0002t0001g0037 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.529-5314A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147909877 | |||||||
| chr2:147909943 | TA | T | 7 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(4): Show |
7 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-5241delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147909943 | ||||||
| chr2:147910013 | CTT | C | 3 | a0001c0002t0001g0024 a0001c0002t0001g0130 a0001c0002t0001g0133 |
3 | NA18994.hp2 NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.529-5177_529-5176d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910013 | |||||||
| chr2:147910049 | T | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0272 a0001c0001t0003g0290 others(1): Show |
6 | NA18943.hp1 NA18948.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-5142T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910049 | |||||||
| chr2:147910207 | G | A | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.529-4984G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910207 | |||||||
| chr2:147910347 | T | A | 1 | a0001c0002t0001g0101 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.529-4844T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910347 | |||||||
| chr2:147910552 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.529-4639G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910552 | |||||||
| chr2:147910604 | A | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0229 |
2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.529-4587A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910604 | |||||||
| chr2:147910614 | G | T | 1 | a0001c0002t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.529-4577G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910614 | |||||||
| chr2:147910629 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.529-4562A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910629 | |||||||
| chr2:147910633 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.529-4558A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910633 | |||||||
| chr2:147910704 | C | A | 1 | a0001c0002t0001g0106 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.529-4487C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910704 | |||||||
| chr2:147910940 | C | T | 91 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.529-4251C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147910940 | |||||||
| chr2:147911056 | A | G | 2 | a0001c0004t0001g0261 a0001c0004t0001g0262 |
2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.529-4135A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147911056 | |||||||
| chr2:147911060 | T | A | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529-4131T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147911060 | |||||||
| chr2:147911615 | T | C | 2 | a0001c0002t0001g0091 a0001c0002t0001g0104 |
2 | NA18988.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.529-3576T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147911615 | |||||||
| chr2:147911784 | A | G | 1 | a0001c0001t0003g0293 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.529-3407A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147911784 | |||||||
| chr2:147911808 | A | G | 1 | a0001c0002t0001g0024 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.529-3383A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147911808 | |||||||
| chr2:147911935 | A | T | 1 | a0001c0001t0001g0279 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.529-3256A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147911935 | |||||||
| chr2:147912015 | A | AACTAGCT | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-3173_529-3167d others(9): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147912015 | ||||||
| chr2:147912056 | C | G | 23 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0027 others(20): Show |
23 | HG00423.hp1 HG00738.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.529-3135C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912056 | |||||||
| chr2:147912061 | G | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.529-3130G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912061 | |||||||
| chr2:147912205 | G | C | 128 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(125): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.529-2986G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912205 | |||||||
| chr2:147912206 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.529-2985G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912206 | |||||||
| chr2:147912228 | A | G | 6 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(3): Show |
6 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-2963A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912228 | |||||||
| chr2:147912271 | T | C | 1 | a0001c0002t0001g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.529-2920T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912271 | |||||||
| chr2:147912450 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0148 a0001c0001t0001g0278 others(2): Show |
6 | HG00735.hp2 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-2741A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912450 | |||||||
| chr2:147912633 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529-2558C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912633 | |||||||
| chr2:147912977 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.529-2214G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147912977 | |||||||
| chr2:147913093 | A | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.529-2098A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913093 | |||||||
| chr2:147913104 | T | A | 1 | a0001c0001t0002g0232 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.529-2087T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913104 | |||||||
| chr2:147913250 | G | A | 7 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(4): Show |
7 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1941G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913250 | |||||||
| chr2:147913268 | TTAAC | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0192 a0001c0001t0001g0193 |
4 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1920_529-1917d others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147913268 | ||||||
| chr2:147913532 | G | A | 108 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.529-1659G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913532 | |||||||
| chr2:147913576 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.529-1615C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913576 | |||||||
| chr2:147913593 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.529-1598C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913593 | |||||||
| chr2:147913614 | A | G | 4 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0034 others(1): Show |
4 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1577A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913614 | |||||||
| chr2:147913649 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0018g0014 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.529-1542G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913649 | |||||||
| chr2:147913740 | T | G | 1 | a0001c0002t0001g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.529-1451T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913740 | |||||||
| chr2:147913822 | C | CA | 9 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0185 others(6): Show |
9 | HG01167.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.529-1340dupA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147913822 | ||||||
| chr2:147913822 | CA | C | 31 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(28): Show |
33 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.529-1340delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147913822 | ||||||
| chr2:147913822 | CAA | C | 201 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(198): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.529-1341_529-1340d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147913822 | ||||||
| chr2:147913822 | CAAA | C | 14 | a0001c0001t0001g0260 a0001c0001t0002g0163 a0001c0001t0002g0246 others(11): Show |
14 | HG01069.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.529-1342_529-1340d others(5): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147913822 | ||||||
| chr2:147913822 | CAAAA | C | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.529-1343_529-1340d others(6): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 147913822 | ||||||
| chr2:147913933 | A | G | 1 | a0001c0002t0020g0040 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.529-1258A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147913933 | |||||||
| chr2:147914165 | T | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-1026T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147914165 | |||||||
| chr2:147914181 | G | A | 1 | a0001c0001t0003g0270 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.529-1010G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147914181 | |||||||
| chr2:147914416 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.529-775T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147914416 | |||||||
| chr2:147914426 | A | G | 1 | a0001c0002t0001g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.529-765A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147914426 | |||||||
| chr2:147914451 | C | T | 128 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(125): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.529-740C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147914451 | |||||||
| chr2:147914472 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.529-719C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147914472 | |||||||
| chr2:147914479 | T | C | 3 | a0001c0002t0001g0065 a0001c0002t0001g0070 a0001c0002t0001g0073 |
3 | HG02602.hp2 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.529-712T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147914479 | |||||||
| chr2:147915090 | C | T | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.529-101C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147915090 | |||||||
| chr2:147915164 | T | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.529-27T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 4/10 | chr2 | 147915164 | |||||||
| chr2:147915393 | C | A | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.672+59C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147915393 | |||||||
| chr2:147915714 | A | G | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.672+380A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147915714 | |||||||
| chr2:147915821 | C | T | 104 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0094 others(101): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+487C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147915821 | |||||||
| chr2:147915934 | A | T | 1 | a0001c0002t0001g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.672+600A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147915934 | |||||||
| chr2:147915970 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.672+636C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147915970 | |||||||
| chr2:147915996 | C | T | 283 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(280): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.672+662C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147915996 | |||||||
| chr2:147916093 | G | A | 166 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(163): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.672+759G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916093 | |||||||
| chr2:147916284 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.672+950A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916284 | |||||||
| chr2:147916345 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.673-938T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916345 | |||||||
| chr2:147916622 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.673-661G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916622 | |||||||
| chr2:147916632 | G | A | 128 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(125): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.673-651G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916632 | |||||||
| chr2:147916815 | G | T | 6 | a0001c0001t0002g0150 a0001c0001t0002g0194 a0001c0001t0002g0220 others(3): Show |
6 | HG00408.hp2 HG01496.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-468G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916815 | |||||||
| chr2:147916828 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0200 |
2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.673-455T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916828 | |||||||
| chr2:147916864 | AAAG | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.673-412_673-410del others(3): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 147916864 | ||||||
| chr2:147916985 | A | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0225 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.673-298A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147916985 | |||||||
| chr2:147917155 | C | G | 7 | a0001c0002t0001g0023 a0001c0002t0001g0039 a0001c0002t0001g0075 others(4): Show |
7 | HG00438.hp2 NA18943.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-128C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147917155 | |||||||
| chr2:147917185 | T | G | 1 | a0001c0002t0001g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.673-98T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147917185 | |||||||
| chr2:147917228 | G | C | 91 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.673-55G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 5/10 | chr2 | 147917228 | |||||||
| chr2:147917513 | C | T | 2 | a0001c0002t0001g0047 a0001c0002t0001g0093 |
2 | HG00558.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.816+87C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | chr2 | 147917513 | |||||||
| chr2:147917857 | A | G | 2 | a0001c0001t0003g0188 a0001c0001t0003g0280 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.816+431A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | chr2 | 147917857 | |||||||
| chr2:147918093 | G | C | 1 | a0001c0001t0002g0166 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.817-354G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | chr2 | 147918093 | |||||||
| chr2:147918159 | A | G | 34 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(31): Show |
43 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.817-288A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | chr2 | 147918159 | |||||||
| chr2:147918168 | TA | T | 6 | a0001c0001t0001g0146 a0001c0001t0001g0189 a0001c0001t0006g0187 others(3): Show |
6 | HG02071.hp2 HG02145.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-264delA | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 147918168 | ||||||
| chr2:147918184 | C | A | 1 | a0001c0001t0002g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.817-263C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | chr2 | 147918184 | |||||||
| chr2:147918210 | G | A | 298 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(295): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.817-237G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | chr2 | 147918210 | |||||||
| chr2:147918280 | A | G | 1 | a0001c0002t0001g0186 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.817-167A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 6/10 | chr2 | 147918280 | |||||||
| chr2:147918724 | TTTTAAAA others(5): Show |
T | 1 | a0001c0001t0002g0163 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.962+136_962+147del others(12): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 147918724 | ||||||
| chr2:147918907 | G | T | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.962+315G>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147918907 | |||||||
| chr2:147919045 | C | G | 276 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.962+453C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147919045 | |||||||
| chr2:147919101 | C | T | 1 | a0001c0002t0001g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.962+509C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147919101 | |||||||
| chr2:147919139 | C | T | 2 | a0001c0001t0021g0276 a0001c0002t0001g0139 |
2 | HG00099.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.962+547C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147919139 | |||||||
| chr2:147919564 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.963-666A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147919564 | |||||||
| chr2:147919777 | C | G | 5 | a0001c0001t0001g0190 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG01167.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.963-453C>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147919777 | |||||||
| chr2:147919861 | T | A | 1 | a0001c0002t0001g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.963-369T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147919861 | |||||||
| chr2:147920018 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.963-212T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147920018 | |||||||
| chr2:147920049 | G | A | 1 | a0001c0002t0009g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.963-181G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147920049 | |||||||
| chr2:147920112 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
7 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.963-118C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147920112 | |||||||
| chr2:147920185 | G | C | 1 | a0001c0002t0012g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963-45G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 7/10 | chr2 | 147920185 | |||||||
| chr2:147920472 | A | G | 2 | a0001c0002t0011g0112 a0001c0002t0012g0144 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1077+128A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920472 | |||||||
| chr2:147920513 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1077+169C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920513 | |||||||
| chr2:147920522 | T | A | 1 | a0001c0001t0002g0168 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1077+178T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920522 | |||||||
| chr2:147920591 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1077+247G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920591 | |||||||
| chr2:147920638 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0189 a0001c0001t0001g0256 others(4): Show |
8 | HG00099.hp1 HG01109.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+294G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920638 | |||||||
| chr2:147920710 | G | C | 1 | a0001c0002t0001g0080 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1077+366G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920710 | |||||||
| chr2:147920769 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1077+425G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920769 | |||||||
| chr2:147920982 | C | T | 8 | a0001c0002t0001g0074 a0001c0002t0001g0129 a0001c0002t0001g0132 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077+638C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147920982 | |||||||
| chr2:147921166 | T | C | 1 | a0001c0002t0001g0104 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1077+822T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147921166 | |||||||
| chr2:147921259 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1077+915T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147921259 | |||||||
| chr2:147921546 | G | C | 1 | a0001c0002t0001g0095 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1077+1202G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147921546 | |||||||
| chr2:147921601 | C | A | 1 | a0001c0001t0002g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1077+1257C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147921601 | |||||||
| chr2:147921717 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1078-1256A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147921717 | |||||||
| chr2:147921984 | A | G | 2 | a0001c0001t0002g0194 a0001c0001t0002g0224 |
2 | HG00408.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1078-989A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147921984 | |||||||
| chr2:147922092 | AT | A | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1078-879delT | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 147922092 | ||||||
| chr2:147922153 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-820A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147922153 | |||||||
| chr2:147922175 | C | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0281 |
2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1078-798C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147922175 | |||||||
| chr2:147922691 | G | A | 168 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0009 others(165): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1078-282G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147922691 | |||||||
| chr2:147922727 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0148 a0001c0001t0001g0278 others(2): Show |
6 | HG00735.hp2 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-246A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147922727 | |||||||
| chr2:147922755 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1078-218A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147922755 | |||||||
| chr2:147922858 | G | C | 135 | a0001c0001t0001g0094 a0001c0001t0004g0021 a0001c0001t0004g0022 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1078-115G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147922858 | |||||||
| chr2:147922957 | T | C | 7 | a0001c0002t0001g0023 a0001c0002t0001g0039 a0001c0002t0001g0075 others(4): Show |
7 | HG00438.hp2 NA18943.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-16T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 8/10 | chr2 | 147922957 | |||||||
| chr2:147923193 | A | G | 20 | a0001c0001t0002g0001 a0001c0001t0002g0147 a0001c0001t0002g0151 others(17): Show |
23 | HG01175.hp2 HG02015.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216+82A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923193 | |||||||
| chr2:147923233 | G | A | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216+122G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923233 | |||||||
| chr2:147923276 | G | C | 108 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
116 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1216+165G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923276 | |||||||
| chr2:147923458 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1216+347A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923458 | |||||||
| chr2:147923583 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0229 a0001c0004t0001g0261 others(1): Show |
4 | HG00738.hp2 HG02615.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216+472G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923583 | |||||||
| chr2:147923650 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1216+539G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923650 | |||||||
| chr2:147923943 | A | T | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1216+832A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923943 | |||||||
| chr2:147923952 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1216+841C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147923952 | |||||||
| chr2:147924135 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1216+1024G>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147924135 | |||||||
| chr2:147924426 | A | G | 5 | a0001c0001t0003g0020 a0001c0001t0003g0275 a0001c0001t0003g0302 others(2): Show |
6 | HG00609.hp1 HG00673.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1216+1315A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147924426 | |||||||
| chr2:147924500 | T | G | 1 | a0001c0002t0001g0038 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1216+1389T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147924500 | |||||||
| chr2:147924645 | G | C | 2 | a0001c0001t0002g0194 a0001c0001t0002g0224 |
2 | HG00408.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1217-1386G>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147924645 | |||||||
| chr2:147924661 | T | C | 1 | a0001c0002t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1217-1370T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147924661 | |||||||
| chr2:147925067 | T | A | 4 | a0001c0002t0001g0096 a0001c0002t0001g0097 a0001c0002t0001g0098 others(1): Show |
4 | HG01123.hp2 NA18984.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217-964T>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925067 | |||||||
| chr2:147925086 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1217-945A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925086 | |||||||
| chr2:147925132 | A | C | 1 | a0001c0001t0021g0276 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1217-899A>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925132 | |||||||
| chr2:147925142 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1217-889A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925142 | |||||||
| chr2:147925160 | T | G | 1 | a0001c0002t0001g0103 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1217-871T>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925160 | |||||||
| chr2:147925274 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1217-757C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925274 | |||||||
| chr2:147925550 | T | C | 7 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0272 others(4): Show |
12 | NA18943.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.1217-481T>C | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925550 | |||||||
| chr2:147925629 | C | A | 6 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(3): Show |
6 | HG02622.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1217-402C>A | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925629 | |||||||
| chr2:147925636 | C | T | 1 | a0001c0002t0015g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1217-395C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925636 | |||||||
| chr2:147925970 | C | T | 3 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0111 |
3 | HG01069.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1217-61C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 9/10 | chr2 | 147925970 | |||||||
| chr2:147926241 | C | T | 1 | a0001c0001t0003g0303 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1347+80C>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 10/10 | chr2 | 147926241 | |||||||
| chr2:147926344 | TAA | T | 13 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(10): Show |
13 | HG00738.hp1 HG01175.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1347+185_1347+186d others(4): Show |
ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 147926344 | ||||||
| chr2:147926350 | A | T | 284 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(281): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1347+189A>T | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 10/10 | chr2 | 147926350 | |||||||
| chr2:147926489 | A | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0123 others(2): Show |
5 | HG00408.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1347+328A>G | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 10/10 | chr2 | 147926489 |